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Blood Specimen Collection Kit (Excludes Hiv Testing)

FDA product code OFZ · Class 1 · Anesthesiology

54
Registered devices
6
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2021-04-09Medical Action Industries, Inc. 306Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.

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

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