Data Foundry

Medical device recalls 2015

Neptune 2 Waste Management System Docking Station — Class II medical device recall Z-2524-2015

Terminated recall by Stryker Instruments Div. of Stryker Corporation, reported 2015-09-09, distributed nationwide. The Fluid Coupling Sleeve, a component within the Neptune Waste Management System Docker, may be out of specif

Recall numberZ-2524-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmStryker Instruments Div. of Stryker Corporation, Portage, MI, United States
Recall initiated2015-07-20
Classified2015-09-01
Reported by FDA2015-09-09
Terminated2016-11-07
DistributedNationwide (US)
Countries outside the USAT, CA, ES, FI, HK, NL
Quantity524
Reason classesspecification failure, packaging
Serial numbers1014500943, 1018706353, 1026700963, 1026700983, 1029304973, 1029902633, 1030508943, 1030508973, 1105600593, 1106800193, 1106800303, 1108404343, 1108703723, 1110907113, 1113700083, 1403031233, 1403031333, 1403031433, 1407803853, 1409300153, 1409300173, 1409300213, 1409300333, 1409300343, 1409300363 and 368 more
Model numbers0702-014-000, 0702-014-000U

Product

Neptune 2 Waste Management System Docking Station (120V and 230V), New and Refurbished Product Usage: The Stryker Docking Station (Docker) is a component of the Neptune 2 Waste Management System. The Stryker Rover, another component of the system, is a mobile unit used to suction and collect fluid waste and surgical smoke from a surgical site in an operating room. After collection, the Docker is mated to the Rover and the emptying of fluid waste and cleaning of the canisters occurs automatically. The Actuator Assembly is a component located within the Docker which consists of the fluid coupling parts under a spring loaded cover. Intended Use: The Neptune 2 Waste Management System is intended to be used in the operating room, pathology, surgical centers, and doctor s offices to collect and dispose of surgical fluid waste as well as collect smoke generated from electrocautery or laser devices.

Reason for recall

The Fluid Coupling Sleeve, a component within the Neptune Waste Management System Docker, may be out of specification. This can cut or dislodge the PTFE seal and cause a leak between the Rover and Docker couplers during docking or leaking from the Rover coupler after docking. The potential hazard is waste fluid and/or fresh water dispensed from the Neptune 2 Rover at the incorrect time.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2524-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.