FDA Device Recalls

Recalls /

#194132

Product

Clean Catch Urine Kit NS 178489, AHMU58A

FDA product code
JSMCulture Media, Non-Propagating Transport
Device class
Class 1
Medical specialty
Microbiology
Affected lot / code info
UDI-DI: 00191072120557 Lots 891211, 737211, 699211, 986221

Why it was recalled

Affected products were assembled off-site by individuals who may not have been properly trained.

Root cause (FDA determination)

Process control

Action the firm took

On May 2, 2022, the customer was notified by email. The customer was instructed to destroy or discard affected kits.

Recalling firm

Firm
American Contract Systems, Inc.
Address
2610 Ne Industrial Dr, Ste 220, Kansas City, Missouri 64117-2648

Distribution

Distribution pattern
US distribution in the state of Minnesota.

Timeline

Recall initiated
2022-05-02
Posted by FDA
2022-07-01
Status

Source: openFDA Device Recall endpoint. Recall record ID #194132. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.