FDA Medical Device Recalls (openFDA)
Stryker Instruments Div. of Stryker Corporation: Stryker brand Neptune waste management system, Neptune Rover, 15 amp plug; model 0700-003-000.
- Recall number
- Z-0175-05
- Recalling firm
- Stryker Instruments Div. of Stryker Corporation
- Product
- Stryker brand Neptune waste management system, Neptune Rover, 15 amp plug; model 0700-003-000.
- Status
- Terminated
- Initiated
- 2004-10-12
- Posted
- 2004-11-04
- Terminated
- 2005-03-28
- Reason
- The grounding pin may break inside of the electrical plug, resulting in a shock hazard.
- Root cause
- Other
- Action
- Hospital customers will be sent a recall notice dated 11/09/04, new plugs for installation on their units, and instructions for installation.
- Quantity
- 365
- Distribution
- United States and Canada.
- Lot, serial or model codes
- All units with an Interpower brand AC power plug, which includes serial numbers 0203177 through 0406301403.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FYD
- Firm FEI
- 1811755
- Firm city
- Kalamazoo
- 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