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Dna-Reagents, Mycobacterium Spp.

FDA product code LQF · Class 1 · Microbiology

8
Registered devices
2
Adverse events
2
Recalls
15
510(k) clearances

Devices with this code

ACCUPROBE® — Hologic, Inc.ACCUPROBE® — Hologic, Inc.ACCUPROBE® — Hologic, Inc.ACCUPROBE — Hologic, Inc.ACCUPROBE® — Hologic, Inc.ACCUPROBE® — Hologic, Inc.ACCUPROBE® — Hologic, Inc.ACCUPROBE® — Hologic, Inc.

Recent recalls

DateFirmReason
2008-12-30Gen-Probe IncThis recall has been initiated following the identification of certain assay tubes that do not contain probe reagent. The affected kits may contain a combinatio
2008-12-30Gen-Probe IncThis recall has been initiated following the identification of certain assay tubes that do not contain probe reagent. The affected kits may contain a combinatio

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.