Recall Z-2282-2026

Stryker Corporation · initiated May 6, 2026

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

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

Codes / lots: GTIN 07613327634914, Serial Number 2521008873

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.

FDA-determined cause: Nonconforming Material/Component

Action taken

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 Instruments.Recalls@stryker.com.

Details

Recall number
Z-2282-2026
Initiated
May 6, 2026
Posted by FDA
June 1, 2026
Product code
JCX – Apparatus, Suction, Ward Use, Portable, Ac-Powered
Quantity
1 unit
Distribution
US Nationwide distribution in the state of Indiana.
Recalling firm
Stryker Corporation, Portage, MI

Official FDA recall record