FDA-Device2023-11-01Class II

DiagnosUS hCG Pregnancy Urine Test Strip Format REF 100-12

Universal Meditech Inc.
Hazard

Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk Alcohol Test Strip, DiagnosUS¿ SARS-CoV-2 Antibody (IgG/IgM) Test, HealthyWiser KetoFast" Ketone Test Strips and PrestiBio" Ketone Test Strips without marketing authorization. UMI is also recall their tests because they are going out of business and would not be able to continue fulfilling any post-market responsibilities of these distributed products. UMI claims to hold 510(k)s for the other devices, purchased the intellectual property in 2015 from the previous 510(k) holder, but FDA has been unable to verify this information. The devices may have unknown performance characteristics because the firm is unable to provide any documentation that the devices were manufactured in conformance with the Quality System regulation, including documentation (e.g., DHF) that the distributed devices had not been modified since original clearance in a way that could impact their safety and effectiveness, documentation of controlled storage temperature/humidity, and post-market surveillance documentation, such as complaints and adverse events.

Sold states
U.S.: CA, FL, IL, LA, NJ, NY, TX and WY O.U.S.: Taiwan
Affected count
5,025 tests
Manufactured in
850 I St, N/A, Reedley, CA, United States
Products
DiagnosUS hCG Pregnancy Urine Test Strip Format REF 100-12

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0063-2024

Don't want to check this manually?

We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.

Get the Sunday Brief