Z-2282-2026Class II

Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System

Name: Z-2282-2026 Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Creator: Stryker Corporation
Published: 2026-05-06
License: https://open.fda.gov/license/

Stryker Corp. / initiated 2026-05-06 / Open, Classified / root cause: manufacturing process

FDA source

Stryker Corporation began a recall of Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System on 2026-05-06. FDA classified it as Class II and gives the reason as "It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a...". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-2282-2026
Classification: Class II
Status: Open, Classified
Initiated: 2026-05-06
Posted: 2026-06-01
Recalling firm: Stryker Corp.
Product: Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Product code: JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered
Reason for recall: It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a potential risk of electrical shock due to the device s safety testing being unverifiable.
Root cause tag: manufacturing process
FDA root cause: Nonconforming Material/Component
Action: Stryker issued an URGENT Medical Device Field Action notice to its consignee on 5/6/2026 via FedEx. The notice explained the issue, potential risk and requested the consignee locate and quarantine the device. The consignee was directed to contact their Stryker Sales Rep to help schedule replacement of the affected device. For questions of concerns, contact Brooke Thompson at [email protected].
Quantity in commerce: 1 unit
Distribution: US Nationwide distribution in the state of Indiana.
Product codes and lots: GTIN 07613327634914, Serial Number 2521008873

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2282-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2282-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-06-10	2026-06-01

Product code JCX

K132671Class IIStryker Neptune 2 Waste Managment SystemStryker Corporation / cleared 2013-12-20

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)