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

Recall Z-2676-2014 — The synthetic non-absorbable surgical sutures CARDIOFLON Evolution are composed of polyester [poly(ethylene terephtalate)] braids, coated, with or without PLEDGETS of different sizes. CARDIOFLON Evolution sutures are green dyed (D&C green # 6, CI 61565) and white (undyed). Some packs are composed o

U.S. FDA — Device Enforcement · France · 2014-06-25 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2676-2014
Date of alert: 2014-06-25
Country / jurisdiction: France
Risk level: Class II
Risk type: recall
Brand: Peters Surgical
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 3661522034989

Reported risk: A potential splitting of the surface treatment of the thread ends on certain sutures has recently been identified.

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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