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

Recall Z-2630-2016 — 120 V Neptune 3 Rover, Model Number: 0703-001-000

U.S. FDA — Device Enforcement · United States · 2016-07-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2630-2016
Date of alert
2016-07-01
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)
1606300523
Reported risk: Stryker initiated a voluntary recall of the 120 V Neptune 3 Rover on 07/01/2016, due to a potential for the device to experience system errors causing the device to shutdown if high levels of electromagnetic interference are present in the operating room.
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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