Recall Z-2282-2026— Stryker Corporation

Name: FDA recall Z-2282-2026
Creator: U.S. Food and Drug Administration
Published: 2026-05-06

Class II · Ongoing

Class II FDA medical device recall by Stryker Corporation, initiated 2026-05-06. It names one FDA 510(k) clearance: K132671. Product: Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System. 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..

Recalling firm: Stryker Corporation
Classification: Class II
Status: Ongoing
Initiated: 2026-05-06
Firm location: Portage, MI, United States

510(k) clearances named in this recall

1 on FDA's record

K132671 — STRYKER NEPTUNE 2 WASTE MANAGMENT SYSTEMStryker Corporation·cleared 2013-12-20

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

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

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.