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Open, Classified

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

FDA Recall Z-2282-2026 · Posted 2026-06-01

Recalling FirmStryker Corporation
Recall StatusOpen, Classified
Product CodeJCX
Date Initiated2026-05-06
Product Quantity1 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.

Firm Action

Stryker issued an URGENT Medical Device Field Action notice to its consignee on 5/6/2026 via FedEx. The notice explained the issue, potential risk and requested the consignee locate and quarantine the device. The consignee was directed to contact their Stryker Sales Rep to help schedule replacement of the affected device. For questions of concerns, contact Brooke Thompson at [email protected].

Root Cause

Nonconforming Material/Component

Distribution Pattern

US Nationwide distribution in the state of Indiana.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K132671STRYKER NEPTUNE 2 WASTE MANAGMENT SYSTEMStryker Corporation · 2013-12-20

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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