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.
Other Recalls by Stryker Corporation
- Class II: Risk 10/31/2025
- Class II: Risk 10/31/2025
- Class II: Risk 07/02/2025
- Class II: Risk 06/18/2025
- Class II: Risk 06/18/2025
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.