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

Recall Z-0147-2015 — Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer simplifies open laparoscopy.

U.S. FDA — Device Enforcement · United States · 2013-09-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0147-2015
Date of alert
2013-09-13
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
CooperSurgical, Inc. D.B.A. Lone Star Medical Products
Product category
device
Product type
Devices
Reported risk: CooperSurgical is recalling two lots of 900-863 because the wrong package insert (IFU) was placed into the shipper.
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.

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