Home › BOUND TREE MEDICAL, LLC › Curaplex
Curaplex
BOUND TREE MEDICAL, LLC · Model 1071-11106 · UDI-DI 00810071633607
9
510(k) clearances
11
Adverse events
1
Recalls
224
Facilities
Description
CURAPLEX DISPENSER FOR EMESIS BAG, HOLDS 25 6EA/CS
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-05-30 | DeRoyal Industries Inc | The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside. |
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 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.
