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

Recall Z-1635-2014 — Microline Renew Fenestrated Control Tip Grasper, Single Patient Use, Product Number: 3222 The ReNew Fenestrated Grasper Forceps Tips are intended to cut, grasp, and dissect various abdominal tissue for use in endoscopic, including laproscopic surgical procedures where instruments are introduced o

U.S. FDA — Device Enforcement · United States · 2014-04-14 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1635-2014
Date of alert: 2014-04-14
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Microline Surgical
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00116169

Reported risk: Grasper jaw may break when force is applied to the jaw

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.

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