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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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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.
April 2, 2025Medical DevicesFDA
American Contract Systems, Inc. recalls Brand Name: Banner Health Systems Product Name: Lap Pack - 170307 Model/Catalog Number: BHLP62H Software Version: N/A
Hazard: Sterility assurance with procedure trays
April 2, 2025Medical DevicesFDA
American Contract Systems, Inc. recalls Brand Name: Banner Health Systems Product Name: Cysto Pack Model/Catalog Number: BHCY31E Product Description: Conveni
Hazard: Sterility assurance with procedure trays
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls CRANI PACK, Model/Catalog Number WECR41D, medical procedure kit.
Hazard: During an internal investigation, ACS was unable to confirm that the CODMAN component achieved the required Sterility Assurance Level and therefore is not suitable for sterilization according to ACS procedures.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls VEIN TRAY, Model No UTVT21C UTVT21C02 UTVT21C-03
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls THORACIC PACK , Model No UTTC82Y UTTC82AA-01
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls SPINE LUMBAR PACK , Model No UTSL72AA UTSL72AB
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls OPEN HEART A PACK , Model No UTOH19AI UTOH19AJ-01 UTOH19AJ-02
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls MAJOR VASCULAR PACK , Model No UTMV78X-01 UTMV78Y UTMV78Y-01 UTMV78X-01 UTMV78Y-02
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls GENERAL LAPAROSCOPIC PACK-LF , Model No UTGL53S-06 UTGL53S-07 UTGL53S-08
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls AV FISTULA , Model No UTAV77T
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls NEURO IR TRAY , Model No WENI56J
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls DIAGNOSTIC NEURO IR TRAY , Model No WENE21
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls CV BASIC PUMP PACK , Model No WECV23D
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls LAPAROSCOPY PACK , Model No SFLA02A SFLA02B
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls EAR PACK , Model No SFEA12A
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls LACERATION TRAY , Model No SGLA07A SGLA07B-01 SGLA07B-02 SGLA07B
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls LACERATION TRAY , Model No SGLA07A SGLA07B-01 SGLA07B-02 SGLA07B
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls DELIVERY PACK , Model No SGDV22D-01 SGDV22E
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls TOTAL HIP PACK , Model No SMTH06O SMTH06P
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls CYSTO , Model No SACY80R
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls URO ROBOTIC PACK , Model No LVUR44C LVUR44C-03
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls LABOR & DELIVERY PPS , Model No LLLD64O LLLD64O-01 LLLD64O-02
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls CENTRAL LINE PICC , Model No LLCL44H LLCL44H-01
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls C-SECTION PPS , Model No LLCI66M LLCI66M-02 LLCI66M-03 LLCI66M-04
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls BORN ON ARRIVAL KIT , Model No LLBN11B
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls GENERAL ANGIO PACK , Model Nos LLAP75G LLAP75G-01 LLAP75G-02 LLAP75G-03
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls OPEN HEART ADULT - SIDE A , Model Nos LLOH01I-01 LLOH01I
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls LABOR & DELIVERY PACK, Model Nos LLLD19H
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls LAPAROSCOPY PACK, Model Nos LLLA21J LLLA21J-02
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls C-SECTION PACK, Model Nos LLCS44F LLCS44F-01
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.