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

Recall Z-2563-2016 — Valleylab Laparoscopic Curved Spatula Electrode 45CM Item Code: E277145 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction via a single handset is desira

U.S. FDA — Device Enforcement · United States · 2016-07-08 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2563-2016
Date of alert: 2016-07-08
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Medtronic
Product category: device
Product type: Devices

Reported risk: Potential for compromise of the package resulting in a breach of the sterile barrier

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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