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UASure Blood Uric Acid Test Strip

APEX BIOTECHNOLOGY CORP. · Model UASure I · UDI-DI 04713648766479

LFQ
5
510(k) clearances
1
Adverse events
1
Recalls
3
Facilities

Description

25s

Recalls

DateFirmReason
2016-07-20Sterling Diagnostics, Inc.Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple diagnostic kits due to a recision of the previously extended expiration dates for the kits.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.