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

Recall Z-2761-2016 — Nylon Surgical Suture for human use and vet use, sold under brand name Riverlon, Securolon, Weblon. Product is sterile. Part numbers: 663BK 663BL 664BL 928BK Product Usage: For use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurolo

U.S. FDA — Device Enforcement · United States · 2016-08-05 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2761-2016
Date of alert: 2016-08-05
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Riverpoint Medical, LLC
Product category: device
Product type: Devices

Reported risk: Nylon Surgical Sutures are recalled because the seals may become open during distribution or subsequent packaging.

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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