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 O.B. PACK HOSPITAL 3/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 PERI GYN PACK 5/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 FANFOLD DRAPE 44"X58 60/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 O.R. TOWELS 25/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 ARTHROSCOPY PK 5/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound he
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 LAPAROSCOPY-GYN SURGICAL PACK Used by medical staff to perform surgical procedures and patient care procedures such as
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 ANGIOGRAPHY PACK 5/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 LAPAROSCOPY GYN PK CS/4 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 UTILITY DRAPE END PRODUCT 50PK/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 LAP-CHOLECYSTECTOMY SURGICAL PACK 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 PERY-GYN SURGICAL PACK 6/CS Used by medical staff to perform surgical procedures and patient care procedures such as
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 BASIC PACK 10/CS Used by medical staff to perform surgical procedures and patient care procedures such as
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 GAUZE SPONGE 4"X4" 16 PLY XRD 1280/CS (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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls SURG GOWN POLYREINF LGE CUSTOM 28/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 GOWN POLYREINF XLGE TOWEL/W 24/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 LAPAROSCOPY PACK 6/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 LAPAROSCOPY OB 6/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound he
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 LAPAROSCOPY PK 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 MINOR LAPAROTOMY PK 5/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 CYSTO TUR PACK 5/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound he
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 LABOR & DELIVERY 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 GAUZE SPONGE 4"X4" 16 PLY SOFT 1280/CS 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 LAPAROSCOPY CHOLE 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 CESAREAN PACK 2/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound he
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 MAJOR LAP PACK 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 CESAREAN PACK 3/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound he
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 ANGIODRAPE PACK DAMAS 6/CS Used by medical staff to perform surgical procedures and patient care procedures such as
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 W/OUT GOWN 11/CS Used by medical staff to perform surgical procedures and patient care procedures such as
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-TPSC 3/CS Used by medical staff to perform surgical procedures and patient care procedures such as wo
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 IMPERVIOUS EXTRA LONG 24/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.