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 Angiography Pack, Catalog number 900-1488. Used by medical staff to perform patient care procedures such as wound hea
Hazard: Customed products are being recalled because of 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 ENT Pack, Catalog number 900-1482. Used by medical staff to perform patient care procedures such as wound healing, su
Hazard: Customed products are being recalled because of 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 D&C Laparoscopy Pack, Catalog number 900-1476. Used by medical staff to perform patient care procedures such as wound
Hazard: Customed products are being recalled because of 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 Reyito Urological Pack, Catalog number 900-1460. Used by medical staff to perform patient care procedures such as wou
Hazard: Customed products are being recalled because of 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 Cirugia Cardiovascular Case Cart, Catalog number 900-1415A. Used by medical staff to perform patient care procedures
Hazard: Customed products are being recalled because of 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 Umbilical Vessel Catheter Kit, Catalog number 900-1408. Used by medical staff to perform patient care procedures such
Hazard: Customed products are being recalled because of 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 number 900-1402. Used by medical staff to perform patient care procedures such as wound
Hazard: Customed products are being recalled because of 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 Open Heart Tray, Catalog number 900-1393. Used by medical staff to perform patient care procedures such as wound heal
Hazard: Customed products are being recalled because of 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 Pediatric Lap Pack, Catalog number 900-1383 Used by medical staff to perform patient care procedures such as wound h
Hazard: Customed products are being recalled because of 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 Spine Pack, Catalog number 900-1300 Used by medical staff to perform patient care procedures such as wound hea
Hazard: Customed products are being recalled because of 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 Premium OB Pack, Catalog number 900-1297. Used by medical staff to perform patient care procedures such as wound heal
Hazard: Customed products are being recalled because of 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 Premium Laparotomy Pack, Catalog number 900-1296. Used by medical staff to perform patient care procedures such as wo
Hazard: Customed products are being recalled because of 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 Premium Cesarean Pack, Catalog number 900-1294 Used by medical staff to perform patient care procedures such as woun
Hazard: Customed products are being recalled because of 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 Laminectomy Pack, Catalog number 900-1202. Used by medical staff to perform patient care procedures such as wound hea
Hazard: Customed products are being recalled because of 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 Open Heart Tray, Catalog number 900-1196C Used by medical staff to perform patient care procedures such as wound hea
Hazard: Customed products are being recalled because of 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 OB GYN Pack, Catalog number 900-1192. Used by medical staff to perform patient care procedures such as wo
Hazard: Customed products are being recalled because of 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 900-1176. Used by medical staff to perform patient care procedures such as wound hea
Hazard: Customed products are being recalled because of 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 number 900-1146. Used by medical staff to perform patient care procedures such as wound healing,
Hazard: Customed products are being recalled because of 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 Foley Catheter Kit, Catalog number 900-1139 Used by medical staff to perform patient care procedures such as wound h
Hazard: Customed products are being recalled because of 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 Foley Catheter Kit, Catalog number 900-1127. Used by medical staff to perform patient care procedures such as wound h
Hazard: Customed products are being recalled because of 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 number 900-1091. Used by medical staff to perform patient care procedures such as wound healin
Hazard: Customed products are being recalled because of 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 900-1062. Used by medical staff to perform patient care procedures such as wound hea
Hazard: Customed products are being recalled because of 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 number 900-1061. Used by medical staff to perform patient care procedures such as wound healin
Hazard: Customed products are being recalled because of 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 Chole Pack, Catalog number 900-1059. Used by medical staff to perform patient care procedures such as wou
Hazard: Customed products are being recalled because of 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 900-1042. Used by medical staff to perform patient care procedures such as wound he
Hazard: Customed products are being recalled because of 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 OB Pack, Catalog number 900-1030. Used by medical staff to perform patient care procedures such as wound healing, sut
Hazard: Customed products are being recalled because of 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 Cysto Tur Pack, Catalog number 900-080. Used by medical staff to perform patient care procedures such as wound healin
Hazard: Customed products are being recalled because of 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 Major Laparotomy Pack, Catalog number 900-036. Used by medical staff to perform patient care procedures such as wound
Hazard: Customed products are being recalled because of 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 900-028. Used by medical staff to perform patient care procedures such as wound heal
Hazard: Customed products are being recalled because of 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 900-012. Used by medical staff to perform patient care procedures such as wound healing, su
Hazard: Customed products are being recalled because of 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.