FDA Device Intelligence
Home › COOK INCORPORATED › Gunther Tulip

Gunther Tulip

COOK INCORPORATED · Model G13287 · UDI-DI 00827002132870

MMX Prescription
10
510(k) clearances
404
Adverse events (7 deaths)
1
Recalls
36
Facilities

Description

Gunther Tulip Vena Cava Filter Retrieval Set

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.

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 docs
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.