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

Recall Z-1305-2019 — ConMed Anchor Tissue Retrieval System 15 MM, 1550 ML (3/BX) Catalog Number: TRS175SB2 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during laparoscopic surgery

U.S. FDA — Device Enforcement · United States · 2019-03-21 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1305-2019
Date of alert: 2019-03-21
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Conmed Corporation
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 201902159

Reported risk: Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product

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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