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

Recall Z-1790-2017 — Eye Cataract Pack, part numbers AMS1359 and AMS1359-1 Product packaged in a convenient manner for use in a general clinical procedure

U.S. FDA — Device Enforcement · United States · 2017-03-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1790-2017
Date of alert
2017-03-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Windstone Medical Packaging, Inc.
Product category
device
Product type
Devices
Reported risk: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
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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