Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2243-2014 — CloverSnare 4-Loop Vascular Retrieval Snare. Product is packaged in a Tyvek-film sterilizable outer package and is supplied one pouch in a box. The CloverSnare 4-Loop Vascular Retriever is intended for use in the cardiovascular system to manipulate and retrieve foreign objects, including but not

U.S. FDA — Device Enforcement · United States · 2014-07-17 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2243-2014
Date of alert: 2014-07-17
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Cook Inc.
Product category: device
Product type: Devices

Reported risk: This remedial action is the result of six product complaints associated with separation of the snare from the distal tip of the wire.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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