FDA Recall Terminated

Neptune 2 Rover Ultra Waste Management System

Recall: Z-0903-2014 · Initiated December 30, 2013

Recall

Recall Number
Z-0903-2014
Event Number
67191
Firm
Stryker Instruments Div. of Stryker Corporation
FEI Number
1811755
Product Code
JCX
Status
Terminated
Root Cause
Device Design
Initiated
December 30, 2013
Posted
January 31, 2014
Terminated
January 12, 2016
Address
4100 E Milham Ave, Portage, MI, 49002-9704

Description

Neptune 2 Rover Ultra Waste Management System

Reason

The purpose of this correction is to upgrade the Neptune 2 Waste Management Systems in the field to the recently obtained 510(k) clearance specifications.

Action

On 12/30/13, Stryker sent an URGENT MEDICAL DEVICE UPDATE notification to consignees including government accounts and Sales Representatives, Stryker Canada and 3 in-house accounts and 1 account for lost rovers. Domestic and government consignees were sent the notification by mail FedEx overnight, and Sales Representatives and Stryker Canada were sent the notification by email. Notification described the affected product, instructions for the consignees, and upgrade information. Stryker also stated that a training kit and in-servicing will be provided to consignees. For questions regarding this recall, please contact Stryker Instruments: Monday-Friday 8am-5pm (EST) Neptune Customer Care Center 855-458-7441 or 269-389-2316 [email protected]

Distribution

Nationwide and Canada, Germany, Australia, New Zealand