Stryker Corporation: Device Recall

Recall #Z-0600-2026 · 10/31/2025

Class II: Risk

Recall Details

Recall Number
Z-0600-2026
Classification
Class II
Product Type
Device
Recalling Firm
Stryker Corporation
Status
Ongoing
Date Initiated
10/31/2025
Location
Portage, MI, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
39,148

Reason for Recall

Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.

Product Description

NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN-1001 13g Illumination Sleeve/Fiber

Distribution Pattern

Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Canada, England, Ireland, Italy, Kuwait, Singapore, Slovenia, Spain, and the Netherlands.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.