Class II

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

Stryker Corporation · May 6, 2026

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.

Distribution

US Nationwide distribution in the state of Indiana.

States Affected

NATIONWIDE

Quantity Affected

1 unit

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2282-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Stryker Corporation Medical Device Recall: Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System | SafeCheck