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 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.
September 9, 2015Medical DevicesFDA
Customed, Inc recalls MINOR LAP. PACK 5/CS REV. 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 CESAREAN PACK 4/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 O.B. PACK 4/CS REV. 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 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 OPEN HEART TRAY CUSTOMED 1/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 LABOR & DELIVERY 4/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 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 LAPAROS.CHOLE 3/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 FEMORAL 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 RETINA PACK 7/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 UNIVERSAL 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 Gown, surgical 30/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 LEGGINGS W/7" CUFF 30" x 42" 30/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 DRESSING CHANGE CUSTOMED 50/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 UROLOGY 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 FOLEY CATH KIT 16FR. W/FOLEY S SENSOR 20/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 LAPAROTOMY PK 4/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 D & C LAPAROSCOPY PK 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 ANGIOGRAPHY 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 E.N.T. PK 7/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 IMPLANTE DE ORTHOPEDIA 3/CS 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 UROLOGY CUSTOMED PACK 5/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 WOUND MANAGEMENT CUSTOMED 20/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 UMBILICAL VESSEL CATHETER KIT CUSTOMED 8/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 PLASTIC SURGERY PACK 5/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 OPEN HEART TRAY 1/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 PEDIATRIC LAP PACK 8/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 NEURO SPINE PACK 3/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 PREMIUM ARTHROSCOPY PK CUSTOMED 5/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.