Fresh Recalls

FDAClass II · Medical device · Recall Z-2282-2026 · Recalled June 10, 2026

Neptune Smart Docking Station (120V) recall — Stryker Corporation

Agency report date: June 10, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Neptune Smart Docking Station (120V)
Company / brand
Stryker
Lot / serial / date codes
GTIN 07613327634914, Serial Number 2521008873
Distribution
US Nationwide distribution in the state of Indiana.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Neptune Smart Docking Station (120V)

3. Open the official notice or contact

Official recall ID
Z-2282-2026
Brand
Stryker
Classification
Class II
Units affected
1 unit
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Portage, MI, United States
Firm address
1941 Stryker Way, 49002-9711

Identifying details (verbatim from the notice)

Product codes / lots
GTIN 07613327634914, Serial Number 2521008873
Distribution
US Nationwide distribution in the state of Indiana.
Firm notified the public via
Letter
FDA event ID
98894
Recall initiated
May 6, 2026
FDA classified
June 1, 2026
FDA report date
June 10, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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