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Curaplex
BOUND TREE MEDICAL, LLC · Model 680152-KIT · UDI-DI 00810094575809
OFZ
Prescription
0
510(k) clearances
6
Adverse events
1
Recalls
17
Facilities
Description
Blood Collection Module, Intermediate
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.