UnratedMedical device recall · FDA · Published May 6, 2026
Stryker Neptune Smart Docking Station Recall: Electrical Shock Risk
Stryker recalls Neptune Smart Docking Station (120V) due to potential electrical shock from incomplete safety testing. Affected units may not have passed required testing before shipping.
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.
Take action
Contact the company
📍Recalling firmStryker Corporation1941 Stryker Way · Portage, MI 49002-9711
“Stryker Neptune Smart Docking Station Recall: Electrical Shock Risk.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/49206-stryker-neptune-smart-docking-station-recall-electrical-shock-risk. Based on FDA recall #Z-2282-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2282-2026%22&limit=1).
The FDA announced on May 6, 2026, that Stryker Corporation is recalling one Neptune Smart Docking Station (120V) due to a potential risk of electrical shock. The agency stated the device may not have completed required safety testing prior to shipment.
How to tell if you have it
Stryker Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
UPC 07613327634914
Serial Number 2521008873
The hazard
The FDA said the impacted docking station was not released from manufacturing and may not have completed required testing. This creates a potential risk of electrical shock because the device's safety testing is unverifiable.
Context
GovInfoNow's records show Stryker Corporation has 34 other recalls on record since November 17, 2017. Recent Stryker recalls include the Ahto Dual Spike Tube Set leak issue reported on June 8, 2026, and the FluidSmart Urology Tube Set nonconforming product distribution noted on April 9, 2026. Other recent recalls of similar products include the Philips Allura Xper FD10C Medical System recall (December 15, 2025), the Getinge SERVO-U/N Ventilator Sensor Module recall (June 30, 2026), and the Philips Allura Xper FD10F Medical System recall (December 15, 2025).
How to tell if you have this one
Check for the Neptune Smart Docking Station (120V) with catalog number 0770-100-000 and serial number 2521008873. This unit is part of the Neptune Waste Management System.
Brand
Stryker
Product
Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify the product's catalog number (0770-100-000) and serial number (2521008873) to confirm if it is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution in the state of Indiana.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 35 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2282-2026 (May 6, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2282-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.