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

Recall Z-1995-2012 — Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips Electrosurgical/Monopolar Forceps/Reusable, Model #41604, 510 (k) #K885199. The surgical device is package in non-sterile small plastic tubes. Monopolar Reusable Forceps - are intended for use in cutting and coagulating tissue during surgical pr

U.S. FDA — Device Enforcement · United States · 2012-06-01 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1995-2012
Date of alert: 2012-06-01
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: PSC Industries Inc
Product category: device
Product type: Devices

Reported risk: Firm officials reported to CIN-DO that their Electrosurgical Monopolar Reusable Bayonet Forceps are misbranded in that the label states that the tip size is: (0.5mm) when the tip size actually measures (1.0mm).

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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