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  • Dispositivo 1149
  • Fabricante 31827
  • Evento 1201
  • Implante 0
Device Recall Remel Blood Agar, 5 Sheep Blood REF R01202
  • Modelo / Serial
    Lot Number: 646595 and 646596 Expiration date: 19May2015
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution.
  • Descripción del producto
    Remel Blood Agar (TSA w/sheep blood) plate REF R01202 packaged 10 plates per pack, 10/10-packs per case (100 plates). || Blood agar is a solid medium recommended for use in qualitative procedures for the cultivation of a wide variety of microorganisms and visualization of hemolytic reactions.
  • Manufacturer
    Remel Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Remel Blood Agar, 5 Sheep Blood REF R01202
Device Recall VersaTREK Automated Microbial Detection System
  • Modelo / Serial
    Serial numbers: 0169039201140624, 0169040501140626, 0169050101141007, 0169068601141216, 0169078101150213, 2163X1013, 2164X1013, 2165X1013, 2166X1013, 2167X1013, 2168X1013, 2169X1013, 2170X1013, 2171X1013, 2172X1013, 2173X1013, 2174X1013, 2175X1013, 2176X1013, 2177X1013, 2178X1013, 2179X1013, 2180X1013, 2181X1013, 2182X1013, 2183X1013, 2184X1013, 2185X1013, 2186X1013, 2187X1013, 2188X1013, 2189X1013, 2190X1013, 2191X1013, 2192X1113, 2193X1113, 2194X1113, 2195X1113, 2196X1113, 2199X1113, 2201X1113, 2202X1113, 2203X1113, 2204X1113, 2205X1113, 2206X1113, 2207X1113, 2208X1113, 2209X1113, 2210X1113, 2211X1113, 2212X1113, 2213X1113, 2214X1113, 2216X1113, 2217X1113, 2218X1213, 2219X1213, 2220X1213, 2221X1213, 2222X1213, 2223X1213, 2224X1213, 2225X1213, 2226X1213, 2227X1213, 2228X1213, 2229X1213, 2230X1213, 2231X1213, 2232X1213, 2233X1213, 2234X1213, 2235X1213, 2237X1213, 2238X1213, 2239X1213, 2240X1213, 2241X1213, 2242X1213, 2243X1213, 2245X1213, 2249X0114, 2250X0114, 2251X0114, 2252X0114, 2253X0114, 2254X0114, 2255X0114, 2256X0114, 2257X0114, 2261X0114, 2262X0114, 2263X0114, 2264X0114, 2268X0114, 2269X0114, 2276X0214, 2277X0214, 2278X0214, 2279X0214, 2280X0214, 2281X0214, 2282X0214, 2286X0214, 2287X0214, 2288X0214, 2289X0214, 2290X0214, 2306X0714, 2307X0714, 2309X0714, 2311X0714, 2312X0714, 2314X0714, 2315X0714, 2316X0714, 2317X0714, 2318X0714, 2320X0714, 2321X0814, 2322X0814, 2323X0814, 2330X0814, 2332X0814, 2333X0814, 2334X0814, 2336X0814, 2337X0814, 2338X0814, 2339X0814, 2340X0814, 2342X0814, 2345X0914, 2346X0914, 2347X0914, 2348X0914, 2349X0914, 2352X0914, 2353X0914, 2359X0914, 2365X0914, and 2366X0914;
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide distribution: US (nationwide) to states of AZ, CO, FL, GA, IA, ID, LA, MI, MO, PR, TN, TX, VA, and WA and the countries of Canada, People's Republic of China, Egypt, Finland, France, Indonesia, Israel, Jordan, Kenya, Republic of Korea, Latvia, Romania, Russia, Spain, Thailand, United Kingdom, Uruguay, and Vietnam.
  • Descripción del producto
    VersaTREK Instrument Series 240 REF 6240, Manufactured for Remel Inc. || The VersaTREK System is for cultivating and recovering microorganisms, especially bacteria and yeasts, from blood and other normally sterile bodily fluids.
  • Manufacturer
    Remel Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall VersaTREK Automated Microbial Detection System
Device Recall IMMULITE 2000/IMMULITE 2000 XPi Italian Cypress
  • Modelo / Serial
    Kit lots 206 (exp. 6-30-2015) and 208 (exp. 11-30-2015)
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution-Distributed in the states of Florida, New Mexico and New York and the countries of Australia, Belgium, Chile, Costa Rica, Croatia, Czech Republic, France, Germany, Greece, Guatemala, Israel, Italy, Japan, Kazakhstan, Latvia, Netherlands, Portugal, Romania, Russian Federation, Slovakia, and Spain.
  • Descripción del producto
    IMMULITE 2000/IMMULITE 2000 XPi Italian Cypress 3g Allergy, Catalog # T23L4 (40 test), Siemens Material Number (SMN) 10386079, IVD. || For in vitro diagnostic use with the IMMULITE 2000 Systems Analyzers for the quantitative measurement of allergen-specific IgE in human serum, as an aid in the clinical diagnosis of IgE-mediated allergic disorders.
  • Manufacturer
    Siemens Healthcare Diagnostics, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall IMMULITE 2000/IMMULITE 2000 XPi Italian Cypress
Device Recall VersaTREK Automated Microbial Detection System
  • Modelo / Serial
    Serial numbers: 0169050501141020, 0169059801141031, 0169064701141210, 0169066801150105, 2200X1113, 2215X1113, 2236X1213, 2244X1213, 2272X0214, 2273X0214, 2274X0214, 2275X0214, 2298X0714, 2299X0714, 2300X0714, 2301X0714, 2303X0714, 2304X0714, 2326X0814, 2327X0814, and 2328X0814;
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide distribution: US (nationwide) to states of AZ, CO, FL, GA, IA, ID, LA, MI, MO, PR, TN, TX, VA, and WA and the countries of Canada, People's Republic of China, Egypt, Finland, France, Indonesia, Israel, Jordan, Kenya, Republic of Korea, Latvia, Romania, Russia, Spain, Thailand, United Kingdom, Uruguay, and Vietnam.
  • Descripción del producto
    VersaTREK Instrument Series 528 REF 6528, Manufactured for Remel Inc. || The VersaTREK System is for cultivating and recovering microorganisms, especially bacteria and yeasts, from blood and other normally sterile bodily fluids.
  • Manufacturer
    Remel Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall VersaTREK Automated Microbial Detection System
Device Recall Etest CEFOTAXIME CT 256
  • Modelo / Serial
    1002774320, 1002377890, 1002590470, 1002775330, 1002379610
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - USA (nationwide) to the states of AL, AR, CA, CO, FL, GA, IL, IN, KY, MD, MI, MN, MO, NE, NY, NC, OH, OK, OR, PA, TN, TX, UT, VA, WA, WV and WI., and to the countries of: Austria, Australia, Canada, Switzerland, Germany, Spain, France, United Kingdom, Greece, Hong Kong, India, Italy, Japan, Netherlands, Poland, Sweden, Thailand, Turkey, Saudi Arabia, Philippines, Slovenia, Kuwait, Brazil, Chile, Czech Republic, Algeria, South Africa, Kosovo, Costa Rica, Belarus, Guam, Honduras and Vietnam.
  • Descripción del producto
    Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic.
  • Manufacturer
    BioMerieux SA
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Etest CEFOTAXIME CT 256
Device Recall HardyCHROM VRE Agar
  • Modelo / Serial
    Cat No.: G333 Lot No.: H15055
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Distributed to one U.S. customer in SC.
  • Descripción del producto
    HardyCHROM VRE Agar-RSR || Cat no: GA333 Lot no: H15055 || Expires: 2015-07-04 || Container type: 15x100mm monoplate || Packaged: 10 plates/sleeve || Storage 2 to 8 degrees C on receipt || Chromogenic medium for stool pathogen screening.
  • Manufacturer
    Hardy Diagnostics
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall HardyCHROM VRE Agar
Device Recall Alere i flu, Alere i, Alere Influenza A & B
  • Modelo / Serial
    Lot Number 0073853 (US distribution only)
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution including AR CA CO CT FL GA IA IL IN KS KY LA MA MD ME MO MS NC NE NJ NY OH PA SC TX VA WA WY.
  • Descripción del producto
    Alere i flu, Alere i, Alere Influenza A & B; Part Number (PN) 425-024 || The Alere" i Influenza A & B assay, performed on the Alere" i Instrument, is a rapid molecular in vitro diagnostic test utilizing an isothermal nucleic acid amplification technology for the qualitative detection and discrimination of influenza A and B viral RNA in nasal swabs from patients with signs and symptoms of respiratory infection. It is intended for use as an aid in the differential diagnosis of influenza A and B viral infections in humans, in conjunction with clinical and epidemiological risk factors. The assay is not intended to detect the presence of influenza C virus.
  • Manufacturer
    Alere Scarborough, Inc. dba Binax, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Alere i flu, Alere i, Alere Influenza A & B
Device Recall MacConkey Agar with Ciprofloxacin
  • Modelo / Serial
    Lot number: 15096 and 15107
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    U.S. Nationwide Distribution and the country of: Canada
  • Descripción del producto
    Hardy Diagnostics || MacConkey Agar with CiPRP, 1ug/ml || Container type: 15x100mm monoplate || packaged: 10 plates/sleeve || Product Usage: || MacConkey Agar with Ciprofloxacin is used as a screening medium for the selective isolation of Ciprofloxacin-resistant E. coli from clinical samples.
  • Manufacturer
    Hardy Diagnostics
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall MacConkey Agar with Ciprofloxacin
Device Recall Brain Heart Infusion Broth with Ciprofloxacin
  • Modelo / Serial
    Lot number: 15055, 15083, and 15091
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    U.S. Nationwide Distribution and the country of: Canada
  • Descripción del producto
    Hardy Diagnostics || BHI with CIPRO, 1ug/ml || container type: 16x100mm tube || packaged: 20 tubes/box || Product Usage: || Brain Heart Infusion Broth with Ciprofloxacin, 1ug is for use as pre-enrichment broth for the cultivation of ciprofloxacin-resistant organisms from clinical samples.
  • Manufacturer
    Hardy Diagnostics
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Brain Heart Infusion Broth with Ciprofloxacin
Device Recall PathoDx Strep Grouping Kit
  • Modelo / Serial
    lot 1470133, exp. date 31 Mar 2016
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution, including Puerto Rico and the country of Canada.
  • Descripción del producto
    PathoDx Strep Grouping Kit, REF 62025, packaged 60 tests per kit. || Latex agglutination test for identification of beta-hemolytic streptococci of Lancefield Groups A, B, C, F or G from primary culture plates.
  • Manufacturer
    Remel Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall PathoDx Strep Grouping Kit
Device Recall PathoDx Strep B Grouping Latex
  • Modelo / Serial
    lot 1463129, exp. date 31 May 2016
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution, including Puerto Rico and the country of Canada.
  • Descripción del producto
    PathoDx Strep B Grouping Latex, REF 62031, 3 ml packaged in plastic dropper bottle with a pink cap. || Latex reagent for streptococcal group B; Identify beta-hemolytic streptococci of Lancefield Groups A, B, C, F and G from primary culture plates.
  • Manufacturer
    Remel Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall PathoDx Strep B Grouping Latex
Device Recall MDR Acinetobacter
  • Modelo / Serial
    Lot number: 15092, 15101, 15113 Cat no. G259
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    U.S. Nationwide Distribution and the country of: Canada
  • Descripción del producto
    Hardy Diagnostics || MDR Acinetobacter || container type: 15x100mm monoplate || packaged: 10 plates/sleeve || Product Usage: || MDR Acinetobacter is for the primary selective screening for detection and differentiation of multi-drug resistant (MDR) Acinetobacter baumannii.
  • Manufacturer
    Hardy Diagnostics
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall MDR Acinetobacter
Device Recall BEA (Bile Esculin Agar) with Azide and Vancomycin
  • Modelo / Serial
    Lot number: 15075. 15096, 15107, 15121, 15134, and 15154 Cat no. G103
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    U.S. Nationwide Distribution and the country of: Canada
  • Descripción del producto
    Hardy Diagnostics || BEA Agar with Vancomycin || container type: 15x100mm monoplate || packaged: 10 plates/sleeve || Product Usage: || BEA (Bile Esculin Agar) with Azide and Vancomycin for VRE is used as a direct screening medium in the isolation and presumptive identification of vancomycin-resistant enterococci/group D streptococci, such as Enterococcus faecalis and E. faecium, from fecal and rectal cultures.
  • Manufacturer
    Hardy Diagnostics
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall BEA (Bile Esculin Agar) with Azide and Vancomycin
Device Recall BEA (Bile Esculin Azide) Agar with Vacomycin, Gentamicin, and Amphotericin B
  • Modelo / Serial
    Lot number: 15105 Cat no. G107
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    U.S. Nationwide Distribution and the country of: Canada
  • Descripción del producto
    Hardy Diagnostics || BEA Agar with VGA || container type: 15x100mm monoplate || packaged: 10 places/sleeve || Product Usage: || BEA (Bile Esculin Azide) Agar with Vacomycin, Gentamicin, and Amphotericin B is for the selective isolation of vancomycin resistant enterococci (VRE).
  • Manufacturer
    Hardy Diagnostics
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall BEA (Bile Esculin Azide) Agar with Vacomycin, Gentamicin, and Amphotericin B
Device Recall BEA (Bile Esculin Azide) Broth with Vancomycin
  • Modelo / Serial
    Lot number: 15070 Cat no. R98  Lot number: 14193, 14232, 14251, 14272, and 14329 Cat no.: R72
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    U.S. Nationwide Distribution and the country of: Canada
  • Descripción del producto
    Hardy Diagnostics || BEA Broth with Vancomycin || container type: 13x100mm tube || packaged: 20 tubes/box || fill: 2ml || Product Usage: || BEA (Bile Esculin Azide) Broth with Vancomycin is for the surveillance of vancomycin resistant enterococci (VRE) not to be used for susceptibility reporting
  • Manufacturer
    Hardy Diagnostics
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall BEA (Bile Esculin Azide) Broth with Vancomycin
Device Recall VRE Broth
  • Modelo / Serial
    Lot number: 15021, 15043, 15072, 15126, 15152 Cat no. K103
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    U.S. Nationwide Distribution and the country of: Canada
  • Descripción del producto
    Hardy Diagnostics || VRE Broth, 5ml || container type: 16x100mm tube || packaged: 20 tubes/box || fill: 5ml || Product Usage: || BEA (Bile Esculin Azide) Broth with Vancomycin is for the surveillance of vancomycin resistant enterococci (VRE) not to be used for susceptibility reporting.
  • Manufacturer
    Hardy Diagnostics
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall VRE Broth
Device Recall cobas Liat Analyzer
  • Modelo / Serial
    Production Identifier (Lot/Serial Number): M1-E-00375, M1-E-00380, M1-E-00381, M1-E-00382, M1-E-00389
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    US Distribution to the states of :TX and NC.
  • Descripción del producto
    cobas Liat Analyzer, for in vitro diagnostic use.
  • Manufacturer
    Roche Molecular Systems, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall cobas Liat Analyzer
Device Recall HardyCHROM MRSA
  • Modelo / Serial
    Cat no. G307 Lot no. H15155
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Distributed in the states of VA, PA, NY, NJ, IL, OH, and MD.
  • Descripción del producto
    HardyCHROM MRSA || Cat no: G307 Lot no: H15155 || Expires: 2015-08-13 || Container Type: 15x100mm monoplate || Packaged: 10 plates/sleeve || Storage: 2-8C on receipt. Light Sensitive. || In vitro diagnostic || www.HardyDiagnostics.com
  • Manufacturer
    Hardy Diagnostics
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall HardyCHROM MRSA
Device Recall Dimension Vista beta2Microglobulin Flex Reagent Cartridge (B2MIC)
  • Modelo / Serial
    Lot Number:15037MA; ExpDate: 2016-07-14 Lot # 15175MA; ExpDate: 2015-11-17; Lot # 15204MA; Expdate: 2017-01-13;  Lot #15246MA; expdate: 2017-02-26 Lot # 15267MA; expdate: 2017-02-26
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    US Nationwide Distribution in the states of TN, AZ, CT, Fl, CA, NY and WI
  • Descripción del producto
    Dimension Vista B¿2-Microglobulin Flex Reagent Cartridge (B2MIC); || Product Usage: The B2MIC method is an in vitro diagnostic test for the quantitative measurement of B¿2-Microglobulin in human serum, heparinized plasma, EDTA plasma and urine on the Dimension Vista System. Measurements of B¿2-Microglobulin aid in the diagnosis of active rheumatoid arthritis and kidney disease.
  • Manufacturer
    Siemens Healthcare Diagnostics, Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Dimension Vista beta2Microglobulin Flex Reagent Cartridge (B2MIC)
Device Recall Xpert CT /NG Vaginal/Endocervical/ Specimen Collection Kit GXCT/NGSWAB50
  • Modelo / Serial
    Part number: CT/NGSWAB-50: Lot numbers: 46A202C, 46A202D, 46A202E, 46A202F, 46A202G, Flock swab expires end of July 2015. Kit expires October 2015. Lot numbers 26N121H, and 28N134D.- Cleaning swabs expire end of June 2016. Kits expires November 2016.
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide distribution. US nationwide, including North Mariana Islands, Aruba, Canada, Chile, Colombia, Costa Rica, Cyprus, Guam, Guatemala, Italy, Malawi, Micronesia Federated States, Panama, San Marino, South Africa, Spain, Switzerland, and Zimbabwe.
  • Descripción del producto
    Xpert CT /NG Vaginal/Endocervical/ Specimen Collection Kit: || Part number CT/NGSWAB-50; || Microbiology: The Cepheid X pert CT /NG Vagina Endocervical/ Specimen Collection Kit is designed to collect, preserve and transport patient Chlamydia trachomatis and Neisseria gonorrhoeae DNA in endocervical and vaginal specimens from symptomatic and asymptomatic individuals prior to analysis with the Cepheid Xpert CT/NG Assay.
  • Manufacturer
    Cepheid
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Xpert CT /NG Vaginal/Endocervical/ Specimen Collection Kit GXCT/NGSWAB50
Device Recall Xpert CT/NG Urine Specimen Collection Kit GXCT/NGSWAB50
  • Modelo / Serial
    Part number: GXCT/NGURINE-50; Lot numbers: 23E104B, 23E104C, 26N128C, 26N1281, 29N142A, 29N142B, 29N142C, 29N142D, 29N142E, 29N142F, and 29N142G All with transfer pipette expiring end of May, June or July 2016. Collection kits expires in August, September, October of November 2016.
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide distribution. US nationwide, including North Mariana Islands, Aruba, Canada, Chile, Colombia, Costa Rica, Cyprus, Guam, Guatemala, Italy, Malawi, Micronesia Federated States, Panama, San Marino, South Africa, Spain, Switzerland, and Zimbabwe.
  • Descripción del producto
    Xpert CT/NG Urine Specimen Collection Kit || Part number GXCT/NGURINE-50; || Microbiology: Xpert CT/NG Urine Specimen Collection Kit is designed to preserve and transport Chlamydia trachomatis and Neisseria gonorrhoeae DNA in first-catch male and female urine specimens from symptomatic and asymptomatic individuals prior to analysis with the Cepheid Xpert CT/NG Assay.
  • Manufacturer
    Cepheid
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Xpert CT/NG Urine Specimen Collection Kit GXCT/NGSWAB50
Device Recall Access Thyroglobulin Assay
  • Modelo / Serial
    Catalogue number: 33860 Lot numbers: 431990 434727 430969 522896 523251  Expiration date: 10/31/16 12/31/16 08/31/16 04/30/17 05/31/17
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution-US (nationwide) including Puerto Rico and the countries of Algeria, Australia, Austria, Belgium, Bolivia, Brazil, Bulgaria, Canada, Chile, China, Colombia, Czech Republic, Egypt, France, Germany, Greece, Honduras, Hong Kong, Hungary, India, Ireland, Israel, Italy, Japan, Korea, Republic of, Lebanon, Lithuania, Mexico, Morocco, New Zealand, Oman, Philippines, Portugal, Qatar, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, Spain, Sweden, Switzerland, Taiwan, Turkey, United Kingdom, Vietnam and Yemen.
  • Descripción del producto
    Access Thyroglobulin Assay; 100 determinations, 2 packs, 50 tests/pack. For the quantitative determination of thyroglobulin levels in human serum and plasma using the Access Immunoassay Systems.
  • Manufacturer
    Beckman Coulter Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Access Thyroglobulin Assay
Device Recall BBL Vancomycin Screen Agar
  • Modelo / Serial
    catalog number 222204.  Lot numbers 5041659, 5064921, 5076659, 5083712, 5097504, 5105955, 5130907, 5139626, and 5147941
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (nationwide) Distribution to the states of: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, PA, RI, SC, TN, TX, UT, VA, WA, WI and WV., and to the countries of : Canada, Colombia, India, Mexico and Europe.
  • Descripción del producto
    Vancomycin Screen Agar
  • Manufacturer
    Becton Dickinson & Co.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall BBL Vancomycin Screen Agar
Device Recall BBL Enterococcus Screen Agar QUAD Plate
  • Modelo / Serial
    catalog number 222201.  Lot numbers 5064938, 5085954, 5105509, and 5133580
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (nationwide) Distribution to the states of: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, PA, RI, SC, TN, TX, UT, VA, WA, WI and WV., and to the countries of : Canada, Colombia, India, Mexico and Europe.
  • Descripción del producto
    Enterococcus Screen Agar QUAD Plate
  • Manufacturer
    Becton Dickinson & Co.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall BBL Enterococcus Screen Agar QUAD Plate
Device Recall Oxoid Gentamicin Anticrobial Susceptibility Testing Disc
  • Modelo / Serial
    Lot 1686823, expiry 30 June 2018
  • Clasificación del producto
    Immunology and Microbiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution including IL, GA, FL, NC, CA, AL, MA, IN, MO, NY, TX, VA, KS, and IA. Product was also distributed to Puerto Rico.
  • Descripción del producto
    Oxoid Gentamicin Antimicrobial Susceptibility Testing Disc (CN10), REF# CT0024B packaged in packs of 5 cartridges - 50 disc/cartridge. || Used in the semi-quantitative agar diffusion test method for in vitro susceptibility testing to assist in the determination of a suitable antibiotic agent for treatment purposes.
  • Manufacturer
    Remel Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Oxoid Gentamicin Anticrobial Susceptibility Testing Disc
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Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.