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Remel

REMEL, INC. · Model R21143 · UDI-DI 00848838022982

JWX
10
510(k) clearances
12
Adverse events
7
Recalls
8
Facilities

Description

BactiStaph Latex 450TST/KT

Recalls

DateFirmReason
2022-11-09Biomerieux IncAs the temperature and time out of range was exceeded, product performances cannot be guaranteed
2011-12-21bioMerieux, Inc.Reports of false negative results in organism identification.
2010-01-15NERL Diagnostics CorporationUnreactive Staph latex reagent
2010-01-15NERL Diagnostics CorporationUnreactive Staph latex reagent
2009-07-20Remel, IncThe products may give false positive results with some non-Staphylococcus aureus strains
2009-07-20Remel, IncThe products may give false positive results with some non-Staphylococcus aureus strains
2008-10-07Remel, IncControl and test wells are reversed on some of the reaction cards.

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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.