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ACS
AMERICAN CONTRACT SYSTEMS, INC. · Model UIST11F · UDI-DI 00191072107268
0
510(k) clearances
6
Adverse events
1
Recalls
16
Facilities
Description
#1 SPECIMEN TUBE PK,STRL F/G (PS 907131)
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. |
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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.