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Medical Action Industries
MEDICAL ACTION INDUSTRIES INC. · Model 71824 · UDI-DI 10809160016640
0
510(k) clearances
51
Adverse events
4
Recalls
24
Facilities
Description
Kit: Central Line Dres 20/Cs
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-09-08 | Medical Action Industries, Inc. 306 | The ChloraPrep 3ml kit component has a shorter expiry date than the labeled kit expiry date. |
| 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. |
| 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. |
| 2020-05-04 | Resource Optimization & Innovation LLC | There is a potential for the product to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field. |
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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.