Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
FDA device recall Z-2282-2026 · posted 2026-06-01 · Open, Classified
Recall details
- Recalling firm
- Stryker Corporation
- 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.
- 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.
- Root cause
- Nonconforming Material/Component
- Status
- Open, Classified
- Product code
- JCX
- Quantity affected
- 1 unit
- Distribution
- US Nationwide distribution in the state of Indiana.
- Date initiated
- 2026-05-06
- Date posted
- 2026-06-01
- Location
- Portage, MI
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| STRYKER NEPTUNE 2 WASTE MANAGMENT SYSTEM (K132671) | Stryker Corporation | 2013-12-20 |