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: 900064 WOUND CLOSURE TRAY II Used by medical staff to perform surgical procedures and patient care pr
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: 900063 WOUND CLOSURE TRAY I 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: 900052 MINOR PROCEDURE SURGICAL PACK Used by medical staff to perform surgical procedures and patien
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: 900036 LAPAROTOMY 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: 900032 UNIVERSAL DRAINAGE TRAY 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: 900028 LAPAROSCOPY SURGICAL PACK
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: 900020 IRRIGATION TRAY WITH IRRIGATION BULB SYRINGE Used by medical staff to perform surgical 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: 900012 OB SURGICAL 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: 900010 SUTURE REMOVAL KIT 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: 9001771 MAYO STAND COVER STERILE 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 C-SECTION PK 2/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 PERI GYN PACK 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 LAPAROTOMY PACK 3/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 ARTHROSCOPY PK L/F 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 CATARACT 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 C-SECTION SURGICAL PACK 2/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 PLASTIC SURGERY PACK 5/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 CURATION KIT 10/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound heal
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
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 UROLOGY PACK 5/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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls CESAREAN PK 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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls LAPAROTOMY PACK CS/6 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 FEMORAL ANGIOGRAPHY PACK 4/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 GENERAL MINOR PK 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 SKIN STAPLE REMOVER KIT 80/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 INCISION AND DRAINAGE TRAY 50/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 CARPAL TUNEL LARGE SURGICAL PACK, 6/CS 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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls ORTHO-IMPLANT SURGICAL PACK, 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 ARTHROSCOPY SURGICAL PACK 4/C 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 CESAREAN PACK 5/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound heal
Hazard: Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.