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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls LAPAROSCOPY PACK 2/CS Used by medical staff to perform surgical procedures and patient care procedures such as wou
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls FACE PACK FJG 8/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound hea
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls TUMMY TUCK PACK-FJG 6/CS Used by medical staff to perform surgical procedures and patient care procedures such as w
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls FACE LIFT 4/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound hea
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls BREAST PACK-BOD 6/CS Used by medical staff to perform surgical procedures and patient care procedures such as wou
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls HAIR RESTORATION PACK-THR 12/CS Used by medical staff to perform surgical procedures and patient care procedures su
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls OBSTETRICAL SURGICAL PACK 4/CS Used by medical staff to perform surgical procedures and patient care procedures s
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls CYSTO TUR PACK BASIC 8/CS Used by medical staff to perform surgical procedures and patient care procedures s
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls ORTHOPEDIC PACK BASIC 5/CS Used by medical staff to perform surgical procedures and patient care procedures suc
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls BASIC PACK 8/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound hea
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls LAPAROTOMY SURGICAL PACK 3/CS Used by medical staff to perform surgical procedures and patient care procedures such
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls URETHRAL CATHETER TRAY CUSTOMED 50/CS Used by medical staff to perform surgical procedures and patient care procedures
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls SUCTION CATHETER KIT CUSTOMED 50/CS Used by medical staff to perform surgical procedures and patient care procedure
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls SHOULDER PACK 3/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound h
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls REEMPLAZO DE RODILLA Y CADERA 2/CS Used by medical staff to perform surgical procedures and patient care procedures
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls SHOULDER ARTHROSCOPY PACK 2/CS Used by medical staff to perform surgical procedures and patient care procedures suc
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls TUMMY TUCK & BREAST PACK-RFMHI 6/CS 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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls FACE PACK MRT 8/CS CUSTOMED Used by medical staff to perform surgical procedures and patient care procedures such a
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls OPEN HEART PACK 1/CS Used by medical staff to perform surgical procedures and patient care procedures such as woun
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls SHOULDER PACK 6/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound hea
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls EXTREMITY PACK 4/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls HIP AND KNEE REPLACEMENT 3/CS Used by medical staff to perform surgical procedures and patient care procedures su
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls ARTHROSCOPY PACK 3/Cs Used by medical staff to perform surgical procedures and patient care procedures such as wound h
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls GOWN COOL IMPEV. XLGE BREATHABLE 24/CS CUSTOMED 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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls GOWN SURG. POLY REINF. XL XLONG 40/CS CUSTOMED 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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls GOWN SURG. POLY REINF. XL XLONG 40/CS CUSTOMED 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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls O.B. PACK 5/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound h
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls LAPAROTOMY PACK 4/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound h
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls SHOULDER PACK (I) (2) 6/CS CUSTOMED 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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls MINOR PACK 4/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound heali
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.