Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Summary
The FDA issued a Class II for Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the N by Stryker Corporation. Reason: It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed requir.
Details
Source
Device Recall
External ID
Z-2282-2026
Action Date
2026-06-10
Status
Ongoing
Category
device
Product Description
Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Lot/Code Info: GTIN 07613327634914, Serial Number 2521008873
Quantity Affected: 1 unit
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-06
Company
Portage, MI
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 169 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Stryker Corporation has 98 FDA actions in our database, including 90 recalls and 8 clearances.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Stryker Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Stryker Corporation have FDA actions?
Stryker Corporation has 98 FDA actions in our database, including 90 recalls and 8 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-2282-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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