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RECOVERY CONE®
Bard Peripheral Vascular, Inc. · Model FBRC · UDI-DI 00801741040948
MMX
Prescription
10
510(k) clearances
398
Adverse events (7 deaths)
1
Recalls
36
Facilities
Description
RECOVERY CONE® Removal System
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-07-17 | Cook Inc. | This remedial action is the result of six product complaints associated with separation of the snare from the distal tip of the wire. |
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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.