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Amplatz Goose Neck™

MEDTRONIC, INC. · Model GN500 · UDI-DI 00763000762353

MMXDXE Prescription
1
510(k) clearances
398
Adverse events (7 deaths)
1
Recalls
36
Facilities

Description

SNARE GN500 GOOSENECK SNARE V02

Recalls

DateFirmReason
2014-07-17Cook 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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Data 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.