Home / Brands / SPS Sterilization
SPS Sterilization Recalls
15 recalls on record · September 19, 2018 to September 19, 2018 · Medical Devices
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Vascular Solutions Venture Rx Catheter, 6F, resterilized.
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Self-Expanding Stent, 10MM X 94MM | 135CM, resterilized.
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Transhepatic Biliary Self-Expanding Stent, 8MM X 80MM | 7
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Boston Scientific Wallstent Enteral Endoprosthesis Colonic/Duodenal Stent, 22MM X 90MM, resterilized.
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding Stent, 24MM X 70MM | 75CM L, resterilized.
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding Stent, 22MM X 45MM | 75CM L, resterilized.
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Boston Scientific Wallstent Endoprosthesis Tracheobronchial Transhepatic Biliary Self-Expanding Stent, 12MM X 90MM | 75C
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Edwards Lifesciences Optisite Arterial Perfusion Cannula, 22F X 24CM, resterilized.
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Edwards Lifesciences Femoral Venous Cannula, 20F X 55CM, resterilized.
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Edwards Lifesciences Femoral Venous Cannula, 18FR, resterilized.
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula, 29/37F (9.6/12.3MM) X 37CM (14.5"), resterilized.
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula, 34F (11.3MM) X 40CM (16"), resterilized.
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula, 38FRX40CM, resterilized.
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Edwards Lifesciences EZ Glide Aortic Cannula, 24F x 37.6CM, resterilized.
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
September 19, 2018Medical DevicesFDA
SPS Sterilization, Inc recalls Edwards Lifesciences Aortic Perfusion Cannula, 24F x 30CM, resterilized.
Hazard: The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.