Neptune recallZ-2282-2026 · Stryker Corporation · initiated May 6, 2026
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Stryker Corporation or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
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 root cause category: Nonconforming Material/Component
What the company is doing
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].
Recall details
- Recall number
- Z-2282-2026
- Status
- Open, Classified
- Initiated by the company
- May 6, 2026
- Posted by the FDA
- Jun 1, 2026
- Recalling firm
- Stryker Corporation
- Quantity
- 1 unit
- Product code
- JCX
- FDA submissions
- K132671
- Distribution
- US Nationwide distribution in the state of Indiana.
Product description
Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Code information (models, lots, serial numbers)
GTIN 07613327634914, Serial Number 2521008873
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- Neptune 0770100000Stryker Corporation · APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED1 recall0 reports
Product lines
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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