Neptune Smart Docking Station recall (Stryker Corporation)
Medical deviceClass IIOngoing
Summary: Stryker Corporation is recalling Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System. Reason: 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.
What is being recalled
Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Why
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.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution in the state of Indiana. (states named: Indiana)
How to tell if yours is affected
GTIN 07613327634914, Serial Number 2521008873
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-2282-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | May 6, 2026 |
| Reported | June 10, 2026 |
| Company | Stryker Corporation |
| Company location | Portage, MI, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 1 unit |
More recalls from Stryker Corporation · all medical device recalls · recalls from May 2026