Z-0175-05

Stryker brand Neptune waste management system, Neptune Rover, 15 amp plug; model 0700-003-000

Name: Z-0175-05 Stryker brand Neptune waste management system, Neptune Rover, 15 amp plug; model 0700-003-000
Creator: Stryker Instruments Div. of Stryker Corporation
Published: 2004-10-12
License: https://open.fda.gov/license/

Stryker Corp. / initiated 2004-10-12 / Terminated

FDA source

Stryker Instruments Div. of Stryker Corporation began a recall of Stryker brand Neptune waste management system, Neptune Rover, 15 amp plug; model 0700-003-000 on 2004-10-12. The reason FDA records is "The grounding pin may break inside of the electrical plug, resulting in a shock hazard". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0175-05
Status: Terminated
Initiated: 2004-10-12
Posted: 2004-11-04
Terminated: 2005-03-28
Recalling firm: Stryker Corp.
Product: Stryker brand Neptune waste management system, Neptune Rover, 15 amp plug; model 0700-003-000.
Product code: FYD Apparatus, Exhaust, Surgical
Reason for recall: The grounding pin may break inside of the electrical plug, resulting in a shock hazard.
FDA 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 in commerce: 365
Distribution: United States and Canada.
Product codes and lots: All units with an Interpower brand AC power plug, which includes serial numbers 0203177 through 0406301403.

Product code FYD

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)