Lower riskMedical device recall · FDA · Published July 9, 2026
Urinary Clean Catch Kit Recalled Due to Incorrect Expiration Date
Medical Action Industries recalls 4,000 units of Urinary Clean Catch Kit (Lot 333606) with an incorrect expiration date of March 31, 2027 instead of February 28, 2027.
An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027.
✎ GovInfoNow plain-language explainer
Medical Action Industries recalls 4,000 units of Urinary Clean Catch Kit (Lot 333606) due to an internal data-entry error that labeled the expiration date as March 31, 2027 instead of February 28, 2027. This error does not affect the product's safety but requires correction to ensure proper use. Read more at govinfonow.com/recall/1629887-medical-action-industries-inc-306-recalls-generic-name-kit-urine.
“Urinary Clean Catch Kit Recalled Due to Incorrect Expiration Date.” GovInfoNow, updated October 21, 2026. https://govinfonow.com/recall/1629887-medical-action-industries-inc-306-recalls-generic-name-kit-urine. Based on FDA recall #Z-0069-2027 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0069-2027%22&limit=1).
The FDA announced on July 9, 2026, that Medical Action Industries is recalling Urinary Clean Catch kits due to an incorrect expiration date. The hazard involves kit lot 333606 being labeled with a March 31, 2027, date instead of February 28, 2027.
How to tell if you have it
Brand: Medical Action Industries
Product: Urinary Clean Catch Kit
Model/Catalog Number: 76769
Lot Number: 333606
UDI-DI: 20809160118228
The hazard
An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027.
Context
GovInfoNow's records show Medical Action Industries, Inc. 306 has 15 other recalls on record since 2019-12-02. Other recent recalls include the Medical Action Industries Epidural Pain Kit Recall (2026-07-23), the Medical Action Industries Blood Culture Kits Risk Localized Infection Due to Packaging Seal (2026-07-23), and the Medical Action Industries Dialysis Change Tray Clear Sequence: Silicone Seal Risk (2026-05-21). Other recent recalls of similar products include LimFlow Vector Product Recall: Incorrect Expiration Date Hazard (2025-12-05) and Medtronic Pocket Adaptor Kits with Incorrect Use-By Dates Recalled (2026-05-13).
How to tell if you have this one
Check for the model number 76769 and lot number 333606 on the kit's packaging. The kit was distributed in California and sold between 2026 and 2027.
Brand
Medical Action Industries
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Expiration Date
Verify the expiration date on the kit's packaging matches February 28, 2027, not March 31, 2027.
Where it went and when
Where it was distributed
Distributed in California.
Listed by the agency
Not listed
FDA distribution: “U.S.: CA O.U.S.: N/A” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California.
Recall timeline
FDA published this recall 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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-0069-2027 (July 9, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0069-2027 to see it in context.
Plain-language summary written by qwen3:4b on October 21, 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.