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

Recall Z-1096-2025 — PROLENE Polypropylene Suture, REF: EH7585H, 8706H, 8833H, 8963H, 8935H PROLENE Suture is indicated for use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurosurgical procedures.

U.S. FDA — Device Enforcement · United States · 2024-12-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1096-2025
Date of alert
2024-12-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ethicon, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10705031097254
Reported risk: Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could introduce pathogens to the patient and cause infection.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.