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.
Stryker is recalling a specific Neptune Smart Docking Station model because it may not have completed safety testing before shipping, creating a risk of electrical shock. This affects facilities that received this unit with the serial number 2521008873.
The docking station may not have completed required safety testing before shipping, which could lead to electrical shock if the device is used. This issue arises because the product was not properly verified for safety before being sent to customers.
Facilities that received the Neptune Smart Docking Station with serial number 2521008873 are affected. Workers using this station in waste management operations are at risk.
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.
Verify the product's catalog number (0770-100-000) and serial number (2521008873) to confirm if it is affected.
The product may not have completed required safety testing before shipping, creating a potential risk of electrical shock.
The official recall notice does not specify a remedy or action steps for affected units.
The recall states a potential risk of electrical shock, but does not specify if this could cause serious injury.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2282-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2282-2026 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
