Cl II Stryker 120 V Neptune 3 Rover

Company: Stryker Instruments Div. of Stryker Corporation
Date of Enforcement Report 8/30/2016
Class lI:

PRODUCT

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

REASON
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.

RECALLING FIRM/MANUFACTURER
Stryker Instruments Div. of Stryker Corporation, Porage, MI on 8/23/2016. Voluntary: Firm Initiated recall is ongoing.

VOLUME OF PRODUCT IN COMMERCE
78

DISTRIBUTION
Domestic:MI, CA, ID, IA VA/DOD: None Foreign: None

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About the author

Amy enjoys researching and writing about developments in medical technology and how that intersects with US law. She received her J.D. from the University of Florida Levin College of Law in 2020 and now works as a Regulatory Associate for SoftwareCPR®, a general-purpose regulatory consulting firm that is recognized globally for their expertise with standards and national regulations pertaining to medical device, mobile medical app, and HealthIT software.

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