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Atrieve™ Vascular Snare Kit
ARGON MEDICAL DEVICES, INC. · Model 382007045 · UDI-DI 20886333004014
MMX
Prescription
1
510(k) clearances
404
Adverse events (7 deaths)
1
Recalls
36
Facilities
Description
Atrieve™ Vascular Snare Kit 7F
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.