FDA recall record

Medical Action Industries, Inc. 306 Generic Name: Kit, Urine, Clean Catch Trade Name: Kit recall — FDA Z-0069-2027

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.

Class IIIclassification
Z-0069-2027official record ID
Oct 14, 2026report date

Recall record at a glance

Official recordZ-0069-2027
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmMedical Action Industries, Inc. 306
Report dateOct 14, 2026
Recall initiation dateJul 9, 2026
Quantity4000
LocationArden, NC, United States

Official product description

Generic Name: Kit, Urine, Clean Catch Trade Name: Kit: Urinary Clean Catch 20/cs Model/Catalog Number: 76769 Lot Number: 333606 UDI-DI: 20809160118228 Software Version: N/A

Why the product was recalled

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.

Distribution information

U.S.: CA O.U.S.: N/A

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.

Medical DeviceMay 13, 2026

Medical Action Industries Inc recall — FDA Z-2007-2026

Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"

Class IFDA: OngoingMedical Action Industries, Inc. 306