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American Contract Systems, Inc.

American Contract Systems, Inc. Recalls

All product recalls associated with American Contract Systems, Inc..

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Recall Summary

Total Recalls

1000

Past Year

891

Class I (Serious)

124

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 4201–4220 of 17593 recalls

ACS Spine and Lumbar Packs (American Contract Systems) – sterilization issue (2022)

Product was sterilized with a higher than specification EO concentration.

Moderate

FDAMar 22, 2022Nationwide• American Contract Systems, Inc.

ACS Surgical Kits (American Contract Systems) – sterilization issue (2022)

Product was sterilized with a higher than specification EO concentration.

Moderate

FDAMar 22, 2022Nationwide• American Contract Systems, Inc.

WAVES WCM Kidney Cassette Module (Waters Medical Systems) – Potential Leakage (2022)

There is a potential for the WCM cassette pump head leaking solution.

Moderate

FDAMar 21, 2022IN, TN• Waters Medical Systems LLC

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ARIA Radiation Therapy System (Varian) – treatment planning issue (2022)

Software issue for treatment plan and image management application may result in mismatch values which could result in treatment in the wrong location

High

FDAMar 21, 2022Nationwide• Varian Medical Systems Imaging Laboratory GmbH Tafernstrasse 7 DATTWIL Baden Switzerland

Natural Dentist Breath Rinse (Revive) – Labeling Mix-up (2022)

Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states active ingredient as Peppermint Oil and Sage Oil and has the wrong UPC

Class IIModerate

FDAMar 21, 2022Nationwide• Revive Personal Products Company

Ultrasonic Gastrovideoscope GF-UC140P-AL5 (Olympus) – Infection Control Risk (2022)

GF-UC140P-AL5 is no longer a compatible endoscope for reprocessing in the OER-Pro and presents an infection control risk to patients

High

FDAMar 18, 2022Nationwide• Olympus Corporation of the Americas

Enoki Mushrooms (Yes Produce) – Listeria Risk (2022)

Listeria

California Department of Public Health sampled product with a result of Listeria monocytogenes

Class IHigh

FDAMar 18, 2022CA, GA, TX• T Fresh Company DBA Yes Produce

PhysiciansCare OTC Drugs (Acme United) – Quality Compliance (2022)

This recall involves the PhysiciansCare brand Extra Strength Non Aspirin, Aspirin, Extra Strength Pain Reliever, Ibuprofen, Medication Station, and Multi-Pack over-the-counter drugs. The products contain aspirin, acetaminophen, or ibuprofen. They are packaged in cardboard boxes of 50, 100, 250, and 500 tablets per box. Product Drug Tablet Amount Extra Strength Non Aspirin Acetaminophen (500 mg) 50 tablets 100 tablets 250 tablets 500 tablets 2 boxes of 100 tablets each Aspirin Aspirin (325 mg) 50 tablets 100 tablets 250 tablets 500 tablets Extra Strength Pain Reliever Acetaminophen (250 mg) Aspirin (250 mg) 100 tablets 250 tablets Ibuprofen Ibuprofen (200 mg) 100 tablets 250 tablets 500 tablets 2 boxes of 100 tablets each Medication Station / Multi-Pack Acetaminophen (500 mg) Aspirin (325 mg) Ibuprofen (200 mg) Antacid (420 mg) 4 boxes of 100 tablets each with outer station 4 boxes of 100 tablets each without outer station The Antacid is not subject to this recall.

Moderate

CPSCMar 17, 2022Nationwide• Acme United of Rocky Mount, North Carolina

ZEISS miLOOP Lens Device (Carl Zeiss) – High Friction Risk (2022)

High friction of the slider can cause the device to stick, or not move as intended.

Moderate

FDAMar 16, 2022AL, AZ, AR +29 more• Carl Zeiss Meditec AG Rudolf-Eber-Str. 11 Oberkochen Germany

Frozen Hash Brown Patties (Cavendish Farms) – Undeclared Allergens (2022)

Undeclared Allergen

Undeclared barley and wheat flour

Class IHigh

FDAMar 13, 2022CT, DE, IN +7 more• Cavendish Farms

Gallant VR Defibrillator (St. Jude Medical) – Bluetooth Malfunction (2022)

Bluetooth malfunction impacting Gallant devices post-implant. The failure causes the device to enter an inductive-only telemetry mode with a loss of Bluetooth communication. The Bluetooth malfunction results in the inability to remotely monitor these devices and resulted in reduced battery longevity.

Moderate

FDAMar 10, 2022Nationwide• St. Jude Medical, Cardiac Rhythm Management Division

Merlin PCS Programmer (St. Jude Medical) – Software Anomaly (2022)

Laceration Risk

Due to a programmer software anomaly under very specific circumstance when executing a pacing capture Decrement Test in-clinic on implantable cardioverter and cardiac resynchronization therapy defibrillator devices, the programmer may continue to execute the Decrement Test instead of terminating the test and restoring the permanent programmed pacing parameters.

Moderate

FDAMar 10, 2022Nationwide• St. Jude Medical, Cardiac Rhythm Management Division