FDA Medical Device Recalls (openFDA)
Stryker Corporation: Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
- Recall number
- Z-2282-2026
- Recalling firm
- Stryker Corporation
- Product
- Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
- Status
- Open, Classified
- Initiated
- 2026-05-06
- Posted
- 2026-06-01
- Terminated
- not on file
- Reason
- 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.
- Root cause
- Nonconforming Material/Component
- 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 Instruments.Recalls@stryker.com.
- Quantity
- 1 unit
- Distribution
- US Nationwide distribution in the state of Indiana.
- Lot, serial or model codes
- GTIN 07613327634914, Serial Number 2521008873
- 510(k) numbers
- K132671
- PMA numbers
- not on file
- Product code
- JCX
- Firm FEI
- 3015967359
- Firm city
- Portage
- Firm state
- MI
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28