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 UROLOGY 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 EENT PACK I (1) 10/CS CUSTOMED 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 (1) (2) 10/CS CUSTOMED 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 EXTREMITY ARM PACK 4/CS HOSP. DR. CENTER 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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls EAR PACK 3/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 LUMBAR PACK 4/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 CENTRAL LINE FULL BODY DRAPE CUSTOMED 28/CS 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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls LAPAROSCOPY-COLORECTAL SURGICAL PACK 2/CS Used by medical staff to perform surgical procedures and patient care proc
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 NEURO PACK 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 EAR PACK 3/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing,
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 SURGICAL PACK 20/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 ARTHROSCOPY 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 LITHOTOMY PACK 10/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 FEMORAL 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 KNEE ARTHROSCOPY PK 4/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 ANGIOGRAPHY PACK CUSTOMED 4/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 GAUZE 2" X 2" PRODUCTION ONLY 1500PK/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 GAUZE SPONGE 2"X2" 8PLY COTTON 1500PK/CS 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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls GAUZE SPONGES 2"x2" 4 PLY ST 2/PK 1500PK/CS 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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls ANGIOGRAPHY PK 4/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 SHOULDER PACK CUSTOMED 3/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 HIGADO Y PANCREA 2/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 ENDOVENOUS CUSTOM PACK 5/CS CUSTOMED 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 OPHTHALMIC 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 HIP ORTHO. 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 OPHTHALMIC PACK 6/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 MAYO STAND COVER W/CSR WRAP 30/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 LAPAROTOMY PACK CUSTOMED 7/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 MINOR LACERATION TRAY CUSTOMED 50/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 UROLOGY PK 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.