Home › Device types › OFZ
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
Motion Medical Distributing — Haslam Medical, Inc.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Curaplex — BOUND TREE MEDICAL, LLCMotion Medical Distributing — Haslam Medical, Inc.Motion Medical Distributing — Haslam Medical, Inc.Therapak — Therapak LLCCuraplex — BOUND TREE MEDICAL, 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.CARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCMedical Action Industries — MEDICAL ACTION INDUSTRIES INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.KidneyCare Specimen Collection Kit — CAREDX, INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Therapak — Therapak LLCMedical Action Industries — 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.
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. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
