FDA Medical devices recall ·
Neptune Smart Docking Station (120V) recall
- Recall number
- Z-2282-2026
- Date
- (initiated May 6, 2026)
- Company / brand
- Stryker Corporation
1941 Stryker Way, Portage, MI, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 1 unit
- Hazard tags
- Electrical shock
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Why was it 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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
GTIN 07613327634914, Serial Number 2521008873
Distribution
US Nationwide distribution in the state of Indiana.
States: Indiana
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2282-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.