CLASS II ONGOING Device recall · Reported 10 Jun 2026 · FDA Enforcement Report

Neptune Smart Docking Station (120V) recalled by Stryker

Stryker is recalling Neptune Smart Docking Station (120V), distributed nationwide in the US. The recall was initiated on 6 May 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesGTIN 07613327634914, Serial Number 2521008873

Quantity recalled1 unit

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2282-2026
FDA event ID: 98894
Recalling firm: Stryker, Portage, MI
Classification: Class II
Status: Ongoing
Recall initiated: 6 May 2026
FDA classified: 1 Jun 2026
Reported: 10 Jun 2026
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Device Malfunction
Device type: Other Medical Devices

Timeline

6 May 2026	Recall initiated by company
1 Jun 2026	Classified by FDA	+26 days
10 Jun 2026	Published in enforcement report	+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.

Product as listed by the FDA

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

Where it was distributed

US Nationwide distribution in the state of Indiana.

Nationwide Indiana

Questions about this recall

Why was it recalled?

Which lots are affected?

GTIN 07613327634914, Serial Number 2521008873

Where was it sold?

US Nationwide distribution in the state of Indiana.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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