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

Recall Z-1641-2015 — ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip, Product Usage: The instruments have application in multiple open or minimally invasive general, gynecologic, urologic, thoracic and pediatric surgical procedures.

U.S. FDA — Device Enforcement · United States · 2015-02-26 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1641-2015
Date of alert: 2015-02-26
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Ethicon Endo-Surgery Inc
Product category: device
Product type: Devices

Reported risk: During an internal inspection of the production process the firm discovered an issue which may cause the cartridge to deploy an incomplete staple line.

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.

Recall Z-1641-2015 — ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip, Product Usage: The instruments have application in multiple open or minimally invasive general, gynecologic, urologic, thoracic and pediatric surgical procedures.

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