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FDA recall, , Moderate risk

Neptune Smart Docking Station

The Neptune Smart Docking Station may not have completed required testing and poses a risk of electrical shock.

What happened

Stryker Corporation, of Portage, Michigan, recalled one Neptune Smart Docking Station (120V), part of the Neptune Waste Management System. The FDA stated that the impacted docking station was not product released from manufacturing and may not have completed required testing prior to being shipped. There is a potential risk of electrical shock due to the device's safety testing being unverifiable.

Stryker began the recall on May 6, 2026, and the FDA added it to its Enforcement Report on June 1, 2026. The unit was distributed in Indiana.

What to do

We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:

  1. A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
  2. Talk to your health care provider before you stop using it.

Is yours affected?

Affected if its UDI-DI is listed.

A UDI-DI is the device identifier printed with the barcode on the device label.

  1. Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System

    UDI-DI
    • 07613327634914
    • 2521008873

Recall details

Company began the recall
Sold in

US Nationwide distribution in the state of Indiana.

Company
Stryker CorporationPortage, Michigan
Risk

Moderate risk

Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.

FDA Class II recall · How risk is rated

Event ID
98894
Recall number
Z-2282-2026
Quantity recalled
1 unit

All recalls from Stryker Corporation

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall

  2. Added to FDA's Enforcement Report · Classified by FDA

  3. Listed on Recall Canary

  4. In FDA's weekly enforcement report

  5. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 2, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)