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

Recall Z-2096-2017 — AMO 25GA Vitrectomy Cutter (Model Number NGP0025) and AMO 20GA Vitrectomy Cutter and Irrigation Sleeve (Model Number NGP0020) Used with the AMO Whitestar Signature System. For ophthalmic use.

U.S. FDA — Device Enforcement · United States · 2017-03-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2096-2017
Date of alert
2017-03-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Abbott Medical Optics Inc. (AMO)
Product category
device
Product type
Devices
Reported risk: Packaging error. 20GA Vitrectomy Cutters may be found in a 25GA package and 25GA Vitrectomy Cutters may be found in a 20GA package.
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.

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