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Nombre Fecha Fecha de inicio País Fuente
Retiro De Equipo (Recall) de Tourniquet Cuffs 2008-08-08 United States USFDA
Retiro De Equipo (Recall) de TURP Electrodes 2008-08-08 United States USFDA
Retiro De Equipo (Recall) de Open & Unused Items - This refers to a sterilization service provided by by SterilMed, Inc. (devices were not reprocessed) for Class 1 and Class 2 devices that were opened, most likely in O. R. suites, in which for whatever reason the physician elected to select a different type of device, different size of device, or maybe elected to not use the device at all in a procedure. This is not a process regulated by FDA, but is included in the recall process as product would still be considered misbranded and or represent a potential risk to patients. || Model #'s: || ABB6543-01 || ABB6544-01 || ACM23116 || ACR800-499 || ACU014719 || ALL2N2704X || ALLASC1201 || ALLF-5501 || ALLSU130-404E || ARTAR-6530 || ARTAR-6540 || ARTAR-6560 || ARTAR-6562 || ARTAR-6564 || ARTAR-6570 || AUT054887 || AUT059035 || AUT059037 || AUT174001 || AUT8886803712 || AUTGIA6025S || BAL60417 || BAR0043620 || BAR0070740 || BAR0601110 || BAR072231 || BARBRD100R || BAX2C4005 || BER610 || BIO418200 || BIO631031 || BOUTC001NSKA || CARASU1510 || COD26-1221 || CON130309 || CON130321 || CON134006 || CON1412 || CON29410 || CON29415H || CON29496 || CON60-6085-100 || CON8535 || CON9413 || CON9448 || COO081012 || COO081014 || COOCTI-512N || COOTD-1 || COOZSI1151 || DAV0035280 || DAV0043650 || DEN50-7000 || DEN50-7500 || DER28-0211 || DLP10012 || EDWDSAFE61 || EDWFEMII016A || ETH10BB || ETH2189 || ETH2211 || ETH5BB || ETH6TB45 || ETHBTD05 || ETHPMW35 || ETHPRW35 || ETHPXW35 || ETHUV120 || FUT4549 || GUIOM-9000S || GUIXP-4000 || GYR240060 || GYR240072 || GYR70138000 || GYR7013-8100 || GYR70140257 || JOH2214 || KEN31140240 || KEN31140562 || KEN8884720221 || KEN8888505172 || KIM111 || KIM228 || kim279 || KIM311 || KIM330 || KIM345 || KIM70321 || KIM79043 || KIM79870 || KIM79878 || KIM888 || KIM89601 || KIM95111 || KIM95521 || KIR10-4000 || KIR10-4001 || KIR14-3000 || KRO6003 || LIN9718 || LINESA-5333 || LINESA-5339 || MECEPT03 || MED05897/JP2311 || MED10001S/JP10001 || MED11348/DYNJP2500 || MED14184/JP2414 || MED14184A/JP2414A || MED21394P/JP2302P || MED2457S/JP8303 || MED2505/JP2510 || MED3110A/JP3003A || MED3110S/JP3003 || MED3130S/JP3008 || MED3140S/JP3005 || MED3820A/JP3102A || MED3820S/JP3102 || MED4202S/JP4003 || MED6052-53 || MED8610S/JP8005 || MED91263 || MED96570-021 || MEDDYNJ01201H || MEDDYNJ05933 || MEDDYNJO5933 || MEDDYNJP8201 || MEDSPT-2314/JP2314HD || MEG0012 || MEG0020 || MEG0035H || MEG0039H || MIC390-310 || MIC6131 || MIC6237 || MIC670-308 || MIC710-111 || MIC81010 || MPS5001689 || OLS20-1410KI || ORSORS-300 || Q2M20-1370 || RMITF-3646-0 || SMI4116 || SMI4615 || SMI4616 || SMI71111579 || SMI7204727 || SMI72200195 || SPIXDWIK28 || STR1608-2-59 || STR1608-2-63 || STR206-16 || STR206-546 || STR250-070-530 || STR250-070-540 || STR275-802-000 || STR306-553 || STR350-202-000 || STR3910-075-500 || STR3910-075-501 || STR3910-075-650 || STR3910-075-651 || STR3910-075-800 || STR400-800 || STR501-140-50 || STR5120-103-15 || STR606-563 || STR620-030-301 || STR620-030-407 || STR620-30-301 || SYN55.36E || SYNSDLB || TELDP-40K || TELMDP-40K || TER5842 || TERL7328 || TEX311033-000 || USE00712031 || VALE1450-6 || VALE1510 || VALE2350H || VALE2450H || VALE2505-10FR || VALE2515H || VALE2516H || WAL909009 || WEC528235 || WEL24-6001 || XOM1014242 || XOM10-46001 || XOM1850200 || XOM31-55631 || XOM31-55632 || XOM31-55636 || XOM31-55637 || XOM31-55638 and || XOM8225825 2008-08-08 United States USFDA
Retiro De Equipo (Recall) de Accessory Head Rest for Alphastar Operating Tables United States USFDA
Retiro De Equipo (Recall) de BD PrepStain System United States USFDA
Retiro De Equipo (Recall) de UniCP Compression Forceps (spreader) United States USFDA
Retiro De Equipo (Recall) de VISTA Negative Pressure Wound Therapy Charger 2008-08-07 United States USFDA
Retiro De Equipo (Recall) de NAMIC Custom Angiographic Kit 2008-08-06 United States USFDA
Retiro De Equipo (Recall) de Liquid Bicarbinate United States USFDA
Retiro De Equipo (Recall) de Liquid Bicarbinate United States USFDA
Retiro De Equipo (Recall) de King Systems, DatexOhmeda, Universal Flex2 Breathing Circuit 2008-08-01 United States USFDA
Retiro De Equipo (Recall) de Intera 1.5T and 1.5T Achieva MRI systems United States USFDA
Retiro De Equipo (Recall) de Next Generation Laser United States USFDA
Retiro De Equipo (Recall) de Dimension EXL United States USFDA
Retiro De Equipo (Recall) de Biomet 2.0 MM Stainless Steel (SS) Crimp Sleeve United States USFDA
Retiro De Equipo (Recall) de Hologic United States USFDA
Retiro De Equipo (Recall) de Biopsy Forceps, Cold 2008-08-08 United States USFDA
Retiro De Equipo (Recall) de Taps 2008-08-08 United States USFDA
Retiro De Equipo (Recall) de Reamers 2008-08-08 United States USFDA
Retiro De Equipo (Recall) de Novel VBR Spinal System 2007-08-16 United States USFDA
Retiro De Equipo (Recall) de King Systems, DatexOhmeda, Universal Flex2 Breathing Circuit 2008-08-01 United States USFDA
Retiro De Equipo (Recall) de GreenLine/D Laryngoscope Blades 2007-04-27 United States USFDA
Retiro De Equipo (Recall) de Reamer THandle 2005-08-08 United States USFDA
Retiro De Equipo (Recall) de Reamer THandle 2005-08-08 United States USFDA
Retiro De Equipo (Recall) de 3'" Titanium Skull Pin United States USFDA