Customed Recalls
682 recalls on record · September 10, 2014 to April 20, 2016 · Medical Devices
Recalls by year
14
15
16
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 900345 BASIC SURGICAL PACK Used by medical staff to perform surgical procedures and patient care pro
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9003190 SURG GOWN SMS AMMI IV FULL Used by medical staff to perform surgical procedures and patient
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002940 OBSTETRICAL SURGICAL PACK Used by medical staff to perform surgical procedures and patient c
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002899 CYSTO TUR SURGICAL PACK Used by medical staff to perform surgical procedures and patient ca
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002830 ORTHOPEDIC SURGICAL PACK Used by medical staff to perform surgical procedures and patient ca
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002829 BASIC SURG PACK Used by medical staff to perform surgical procedures and patient care proce
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 900281A LAPAROTOMY PACK Used by medical staff to perform surgical procedures and patient care proced
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 900278 URETHRAL CATHETER TRAY 14FR Used by medical staff to perform surgical procedures and patient
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 900277 SUCTION CATHETER TRAY 14FR WITH SODIUM CHLORIDE 0.9% IRRIGATION Used by medical staff to perfo
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002766 SHOULDER PACK Used by medical staff to perform surgical procedures and patient care procedur
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002726 HIP AND KNEE REPLACEMENT SURGICAL PACK Used by medical staff to perform surgical procedures
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002618 OPEN HEART SURGICAL PACK Used by medical staff to perform surgical procedures and patient c
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002615 EXTREMITY SURGICAL PACK Used by medical staff to perform surgical procedures and patient car
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002614 HIP AND KNEE REPLACEMENT SURGICAL PACK Used by medical staff to perform surgical procedures a
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002609 ARTHOSCOPY PACK Used by medical staff to perform surgical procedures and patient care proce
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002516 LAPAROTOMY SURGICAL PACK Used by medical staff to perform surgical procedures and patient c
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002511 MINOR SURGICAL PACK Used by medical staff to perform surgical procedures and patient care p
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002510 UROLOGY SURGICAL PACK Used by medical staff to perform surgical procedures and patient care
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002469 BASIC SURGICAL PACK IV Used by medical staff to perform surgical procedures and patient car
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002259A LAPAROSCOPY-COLORECTAL SURGICAL PACK Used by medical staff to perform surgical procedures an
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002256 NEUROSURGERY PACK Used by medical staff to perform surgical procedures and patient care pro
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002224 SURGICAL PACK Used by medical staff to perform surgical procedures and patient care procedu
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002193 SHOULDER ARTHROSCOPY SURGICAL PACK Used by medical staff to perform surgical procedures and
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002167 LITHOTOMY SURGICAL PACK Used by medical staff to perform surgical procedures and patient ca
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002164 FEMORAL SURGICAL PACK Used by medical staff to perform surgical procedures and patient care
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9002123 KNEE ARTHROSCOPY SURGICAL PACK Used by medical staff to perform surgical procedures and pat
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9001966 LIVER & PANCREAS SURGERY Used by medical staff to perform surgical procedures and patient c
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9001933 OPHTALMIC SURGICAL PACK Used by medical staff to perform surgical procedures and patient ca
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9001780 OPHTHALMIC SURGICAL PACK Used by medical staff to perform surgical procedures and patient c
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
April 20, 2016Medical DevicesFDA
Customed, Inc recalls Catalog Number: 9001771 MAYO STAND COVER STERILE Used by medical staff to perform surgical procedures and patient ca
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.