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

Recall Z-1025-2019 — Cook Celect Platinum Vena Cava Filter Set for Jugular Vein Approach, Catalog Number GTCFS-65-1-JUG-CELECT-PT Product Usage: The Cook Celect Platinum Filter implant is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the following situations: Pul

U.S. FDA — Device Enforcement · United States · 2019-02-25 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1025-2019
Date of alert: 2019-02-25
Country / jurisdiction: United States
Risk level: Class III
Risk type: recall
Brand: Cook Medical Incorporated
Product category: device
Product type: Devices

Reported risk: Updates to the Instructions for Use.

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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