FDA Class II Recall: Neptune Smart Docking Station (120V), Catalog Number 0770-100-000,… by Stryker Corporation — Recall Details

Key facts

What this classification means

FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote. In this case, the recalling firm is Stryker Corporation and the affected product is described in FDA's record as: Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System. FDA's stated reason for the recall is: 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.. The recall is tracked under FDA recall number Z-2282-2026 and carries a status of Ongoing as of the most recent FDA enforcement report. This classification reflects FDA's assessment of the product defect described above, not a prediction about any specific patient outcome. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do. Recall status can change while FDA and the recalling firm continue corrective actions, so checking the firm's own notice for the most current guidance is recommended.

What consumers should do

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Specifically, check whether the product in your possession matches the description on file with FDA -- Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System -- and the recall number Z-2282-2026. If it matches, stop using or distributing it and contact Stryker Corporation or the point of purchase for return or replacement instructions. Retailers and distributors holding affected inventory should quarantine it and follow the firm's written recall notice. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do.

Stryker Corporation’s FDA history

Argus HQ has recorded 94 total FDA actions tied to Stryker Corporation: 0 warning letters, 94 recalls, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

Has Stryker Corporation had other FDA recalls or enforcement actions?

Yes. Argus HQ has recorded 94 total FDA actions tied to Stryker Corporation, including 94 recalls and 0 warning letters.

What is the FDA recall number for this event?

FDA recall number Z-2282-2026.

What is the current status of this recall?

Status as recorded by FDA: Ongoing.

Where can I verify this recall directly with FDA?

The verbatim FDA record is the source of truth for every recall Argus HQ tracks — always confirm against fda.gov before acting.

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