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.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls C-Section Pack, Catalog # 900-998 Used by medical staff to perform patient care procedures such as wound healing, sut
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Peri Gyn Pack, Catalog # 900-997 Used by medical staff to perform patient care procedures such as wound healing, sutu
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Laparotomy Pack, Catalog # 900-996 Used by medical staff to perform patient care procedures such as wound healing, su
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Arthoscopy Pack, Catalog # 900-982 Used by medical staff to perform patient care procedures such as wound healing, su
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Strabismus And Plastic Pack, Catalog # 900-946 Used by medical staff to perform patient care procedures such as wound
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Cataract Pack, Catalog # 900-944 Used by medical staff to perform patient care procedures such as wound healing, sutu
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls C-Section Surgical Pack, Catalog # 900-921A Used by medical staff to perform patient care procedures such as wound he
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Plastic Surgery Pack, Catalog # 900-920 Used by medical staff to perform patient care procedures such as wound healin
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls , Catalog # 900-913 Used by medical staff to perform patient care procedures such as wound healing, suture removals,
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Arthroscopy Pack, Catalog # 900-902 Used by medical staff to perform patient care procedures such as wound healing, s
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Urology Pack, Catalog # 900-868 Used by medical staff to perform patient care procedures such as wound healing, sutur
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Cesarean Pack, Catalog # 900-851 Used by medical staff to perform patient care procedures such as wound healing, sutu
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Laparotomy Pack, Catalog # 900-848 Used by medical staff to perform patient care procedures such as wound healing, su
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Femoral Angiography Pack, Catalog number 900-796. Used by medical staff to perform patient care procedures such as wo
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls General Minor Pack, Catalog # 900-787 Used by medical staff to perform patient care procedures such as wound healing,
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Neuro Pack, Catalog # 900-752 Used by medical staff to perform patient care procedures such as wound healing, suture
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Carpal Tunnel Surgical Large Pack, Catalog # 900-742A Used by medical staff to perform patient care procedures such a
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Arthroscopy Surgical Pack, Catalog # 900-740A Used by medical staff to perform patient care procedures such as wound
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Cesarean Pack, Catalog # 900-660 Used by medical staff to perform patient care procedures such as wound healing, sutu
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls O.B. Pack, Catalog number 900-645. Used by medical staff to perform patient care procedures such as wound healing, su
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Pery Gyn Pack, Catalog number 900-635. Used by medical staff to perform patient care procedures such as wound healing
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Fanfold Drape, Catalog number 900-633. Used by medical staff to perform patient care procedures such as wound healing
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls O.R. Towels, Catalog number 900-629. Used by medical staff to perform patient care procedures such as wound healing,
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Arthroscopy Pack, Catalog number 900-620. Used by medical staff to perform patient care procedures such as wound heal
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Angiography Pack, Catalog number 900-610. Used by medical staff to perform patient care procedures such as wound heal
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Laparoscopy Gyn Pack, Catalog number 900-605. Used by medical staff to perform patient care procedures such as wound
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Laparoscopy Cholecystectomy Surgical Pack, Catalog number 900-576A. Used by medical staff to perform patient care pro
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Pery GYN Surgical Pack, Catalog number 900-548A. Used by medical staff to perform patient care procedures such as wou
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Laparotomy Basic Pack, Catalog number 900-547 Used by medical staff to perform patient care procedures such as wound
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
December 10, 2014Medical DevicesFDA
Customed, Inc recalls Laparoscopy Pack, Catalog number 900-486. Used by medical staff to perform patient care procedures such as wound heal
Hazard: Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.