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Nombre Fecha Fecha de inicio País Fuente
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de NEONATE 1 DISPOSABLE BLOOD PRESSURE CUFF WITH 1 TUBE, a disposable 1 piece cuff for single patient use only. Sold under the Welch Allyn label with Part #5082-101-1, and sold as part of a multi-pack (1 of each size) with Part #5082-241-9 - firm on label is Welch Allyn, Inc., Skaneateles Falls, NY; Allegiance ''Tactics'' label with Part #30502-110S, firm on label is Allegiance Healthcare Corp., McGaw Park, IL; and Arden label with Part #5084-101-1, firm on label is Arden, Skaneateles, NY. 2004-03-01 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de NEONATE 1 DISPOSABLE BLOOD PRESSURE CUFF WITH 2 TUBES, a disposable 1 piece cuff, for single patient use only. Sold under the Welch Allyn ''Tycos'' label with Part #s 5082-101-2, 5082-101-2CL, and sold as part of a multi-pack (1 of each size) with Part #5082-241-10 - Welch Allyn Inc., Skaneateles Falls, NY; Allegiance ''Tactics'' label with Part #s 30502-110 and 30502-210 - Allegiance Healthcare Corp., McGaw Park, IL; and Arden label with Part #s 5084-101-2 and 633-5084-101-2 - Arden, Skaneateles, NY. 2004-03-01 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de NEONATE 2 DISPOSABLE BLOOD PRESSURE CUFF WITH 1 TUBE, a disposable 1 piece cuff for single patient use only. Sold under the Welch Allyn ''Tycos'' label with Part # 5082-102-1 and sold as part of a multi-pack (1 of each size) with Part #5082-241-9 - Welch Allyn Inc., Skaneateles Falls, NY; Allegiance Healthcare ''Tactics'' label with Part # 30502-111S - Allegiance Healthcare Corp., McGaw Park, IL; and Arden label with Part # 5084-102-1 - Arden, Skaneateles, NY. 2004-03-01 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe and Hypodermic Needle 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe 2017-06-23 United States USFDA
Retiro De Equipo (Recall) de Device Recall TDx/TDxFLx 2002-12-11 United States USFDA
Retiro De Equipo (Recall) de Device Recall Piston Syringe 2017-06-23 United States USFDA