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

Recall Z-1807-2020 — Neptune E-SEP 165mm Blade Electrode, Catalog Number 0703-165-001 - Product Usage: The Neptune E-SEP is an Integrated Smoke Evacuation Pencil (pencil) designed for general electrosurgical applications including cutting and coagulation, and for removing smoke generated by electrosurgery when used in c

U.S. FDA — Device Enforcement · United States · 2020-03-26 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1807-2020
Date of alert: 2020-03-26
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Stryker Instruments Div. of Stryker Corporation
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 16240231

Reported risk: Due to a distribution error, product from the affected lot was shipped expired.

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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