FDA Medical Device Recalls (openFDA)
Stryker Instruments Div. of Stryker Corporation: Neptune 2 Rover Ultra Waste Management System
- Recall number
- Z-0903-2014
- Recalling firm
- Stryker Instruments Div. of Stryker Corporation
- Product
- Neptune 2 Rover Ultra Waste Management System
- Status
- Terminated
- Initiated
- 2013-12-30
- Posted
- 2014-01-31
- Terminated
- 2016-01-12
- 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.
- Root cause
- Device Design
- 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 strykerinstrumentsrecalls@stryker.com
- Quantity
- not on file
- Distribution
- Nationwide and Canada, Germany, Australia, New Zealand
- Lot, serial or model codes
- Manufacturer Part Number 0702-002-000 (230V) All serial numbers
- 510(k) numbers
- ["K132671"]
- PMA numbers
- not on file
- Product code
- JCX
- Firm FEI
- 1811755
- Firm city
- Portage
- Firm state
- MI
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28