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Phlebotomy Blood Collection Kit
FDA product code OFM · Class 2 · Cardiovascular
101
Registered devices
0
Adverse events
2
Recalls
0
510(k) clearances
Devices with this code
CARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCMedical Action Industries — MEDICAL ACTION INDUSTRIES INC.MEDICAL ACTION INDUSTRIES — MEDICAL ACTION INDUSTRIES INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Butterfly Needle Phlebotomy Kit — Labcorp Genetics IncMEDICAL ACTION INDUSTRIES — MEDICAL ACTION INDUSTRIES INC.MEDICAL ACTION INDUSTRIES — MEDICAL ACTION INDUSTRIES INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Avid Trucustom — MEDICAL ACTION INDUSTRIES INC.CARDINAL HEALTH — Cardinal Health 200, LLCMedical Action Industries — MEDICAL ACTION INDUSTRIES INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.MAI-A — MEDICAL ACTION INDUSTRIES INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-04-09 | Medical Action Industries, Inc. 306 | Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. |
| 2010-12-06 | Continental Medical Labs,Inc | Continental Medical labs, Inc, is recalling various lots of Blood Center Kit and Port VAD Kits because Covidien reported that testing could not pick up an O |
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