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Medical Action Industries
MEDICAL ACTION INDUSTRIES INC. · Model 76395 · UDI-DI 10809160131336
OFM
Prescription
0
510(k) clearances
0
Adverse events
3
Recalls
17
Facilities
Description
NA NA Combo No Disposable/Sngle Use FDA Class II Kit No Latex Latex Free Natural Rubber LTX Non Sterile Prescription Use RX
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-23 | Medical Action Industries, Inc. 306 | Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the componen |
| 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 Over-Sulfated Chondro |
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Get your free API keyRead the docsData 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.