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

Recall Z-1994-2012 — Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick Electrosurgical/Bipolar Forceps/Reusable, Model #90-7004 (k) #K982705. The surgical device is package non-sterile into small plastic tubes. Olsen Medical Biopolar Reusable Bayonet Forceps and cords are intended for use in coagulating tissue

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-1994-2012
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 Bipolar Bayonet Forceps 7.75" are misbranded in that the manufacturer symbol was replaced by the expiry symbol on the 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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