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

Recall Z-1180-2023 — Surgipro II Monofilament Polypropylene Sutures Product Description Model Number VP-421X SURGIPROII 4-0 90CM V20 DA7P VP421X VP-435-X SURGIPRO II 4-0 90CM KV5 DA7P VP435X VP-541X SURGIPROII 4-0 BLU 120CM V20DA VP541X VP-542-X SURGIPRO II 3-0 BLU 120CM V20DA VP542X VP-735-X SURGIPRO*II 7-0 60C

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-1180-2023
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): 20884521039534

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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