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

Recall Z-1178-2023 — Surgilon Braided Nylon suture Product Description: 88861883-51 SURGILON* 2-0 BLK 75CM C16 88861915-71 SURGILON* 1 BLK 75CM GS11 88861919-31 SURGILON* 4-0 BLK 7X75CMPCT 88861919-41 SURGILON* 3-0 BLK 7X75CMPCT 88861919-51 SURGILON* 2-0 BLK 7X75CMPCT 88861919-61 SURGILON* 0 BLK 7X75CM PCT 88861

U.S. FDA — Device Enforcement · United States · 2022-12-02 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1178-2023
Date of alert: 2022-12-02
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Covidien, LP
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 20884521073996

Reported risk: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact

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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