American Contract Systems recalls Clean Catch Urine Kit NS 178489, AHMU58A due to potential improper assembly by untrained individuals. Affected lots include 891211, 737211, 699211, 986221.
Affected products were assembled off-site by individuals who may not have been properly trained.
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📍Recalling firmAmerican Contract Systems, Inc.2610 Ne Industrial Dr Ste 220 · Kansas City, MO 64117-2648
✎ GovInfoNow plain-language explainer
American Contract Systems is recalling Clean Catch Urine Kits with specific model numbers because they were assembled by people who might not have been properly trained. This could lead to improper use of the kit, though the recall doesn't mention specific injuries or hazards beyond assembly issues. Read more at govinfonow.com/recall/60741-clean-catch-urine-kit-recall-improper-assembly-risk.
“Clean Catch Urine Kit Recall: Improper Assembly Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60741-clean-catch-urine-kit-recall-improper-assembly-risk. Based on FDA recall #Z-1276-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1276-2022%22&limit=1).
The FDA announced on May 2, 2022, that American Contract Systems Inc. is recalling Clean Catch Urine Kits NS 178489 and AHMU58A due to potential assembly errors by untrained individuals. The agency classified the recall as Class I.
How to tell if you have it
Brand: American Contract Systems
Product: Clean Catch Urine Kit NS 178489, AHMU58A
UDI-DI: 00191072120557
Lots: 891211, 737211, 699211, 986221
Quantity: 274,400 kits
Distribution: Minnesota
The hazard
According to the FDA, affected products were assembled off-site by individuals who may not have been properly trained. The agency classified the recall as Class I.
Context
GovInfoNow's records show American Contract Systems Inc. has had 21 other recalls on record since November 21, 2018. Other recent recalls of similar products include Medical Convenience Kits with Contaminated Wipes Risk Infection (August 10, 2026), American Contract Systems Convenience Kit Recall: Catheters May Not Meet Performance Specs (June 29, 2026), and American Contract Systems Medical Kits Recall: Endotoxin Variability Risk (May 19, 2026). Other recent recalls of similar products include Medline Convenience Kits Recall: Contaminated Components Risk (July 10, 2026), Stryker FluidSmart Urology Tube Set Recall: Nonconforming Products Distributed (April 9, 2026), and Medline convenience kits recalled for potential contamination (July 10, 2026).
How to tell if you have this one
Check for the model number NS 178489, AHMU58A on the kit. Affected lots include 891211, 737211, 699211, and 986221. The kit may have a unique identifier (UDI-DI) starting with 00191072120557.
Brand
American Contract Systems
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1276-2022 (May 2, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1276-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.