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American Contract Systems Recalls
204 recalls on record · November 21, 2018 to May 13, 2026 · Medical Devices
Recalls by year
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22
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26
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 14, 2022Medical DevicesFDA
American Contract Systems, Inc. recalls Various Angiography packs/trays
Hazard: Product was exposed to multiple sterilization cycles without validation for multiple exposures.
July 13, 2022Medical DevicesFDA
American Contract Systems, Inc. recalls Nasopharyngeal sample collection tray for COVID-19 testing, labeled as COVID TEST KIT NONSTERILE 184312, AHCV18A
Hazard: Affected products were assembled off-site by individuals who may not have been properly trained.
July 13, 2022Medical DevicesFDA
American Contract Systems, Inc. recalls Clean Catch Urine Kit NS 178489, AHMU58A
Hazard: Affected products were assembled off-site by individuals who may not have been properly trained.
May 18, 2022Medical DevicesFDA
American Contract Systems, Inc. recalls ACS Cath Lab Pack
Hazard: Product was sterilized with a higher than specification EO concentration.
May 18, 2022Medical DevicesFDA
American Contract Systems, Inc. recalls ACS Lap Chole Pack
Hazard: Product was sterilized with a higher than specification EO concentration.
May 18, 2022Medical DevicesFDA
American Contract Systems, Inc. recalls ACS IR - Angio Pack
Hazard: Product was sterilized with a higher than specification EO concentration.
May 18, 2022Medical DevicesFDA
American Contract Systems, Inc. recalls 1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack
Hazard: Product was sterilized with a higher than specification EO concentration.
May 18, 2022Medical DevicesFDA
American Contract Systems, Inc. recalls 1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray
Hazard: Product was sterilized with a higher than specification EO concentration.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
June 10, 2020Medical DevicesFDA
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
Hazard: The surgical gowns were manufactured in a facility that is not registered by the FDA.
March 6, 2019Medical DevicesFDA
American Contract Systems, Inc. recalls Bag size #4 Custom Convenience Kits Usage: Surgical convenience kits labeled as the following: a. Tray Name:
Hazard: Potential that product has not reached complete sterilization,
November 21, 2018Medical DevicesFDA
American Contract Systems, Inc. recalls Powdered Surgical Gloves, labeled as: a. Baxter and Ansell brand Powdered Surgical Gloves b. Powdered Surgical Glove
Hazard: Powdered Surgical Gloves are an FDA banned substance.