Data Foundry

Medical device recalls 2025

NICO Myriad Illumination Pack Product No — Class II medical device recall Z-0600-2026

Ongoing recall by Stryker Corporation, reported 2025-12-03, distributed nationwide. Tape used to secure components within packaging contains latex, despite products being labeled as latex-free.

Recall numberZ-0600-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmStryker Corporation, Portage, MI, United States
Recall initiated2025-10-31
Classified2025-11-26
Reported by FDA2025-12-03
DistributedNationwide (US)
Countries outside the USAU, BE, CA, ES, GB, IE, IT, KW, NL, SG, SI
Quantity39,148
Reason classeslabeling
UPC / GTIN / UDI-DI00816744021009, 00816744021016
Lot numbers37AC5163, 37AC5177, 37AE9811, 37AE9942, 37AE9955, 37AJ1438, 37AJ1439, 37BJ0513, 37BJ0516, 37CB3380, 37CB3410, 37CB3416, 37CB3419, 37CD6003, 37CD6005, 37CE3030, 37CJ0204, 37DE4864, 37EB5720, 37EB5721, 37FA4260, 37FA4261, 37GD2216, 37GD2219, 37GJ1603, 37GJ1607, 37IC7023, 37IC7027, 37IJ0208, 37IJ0209, 37JD5753, 37JJ0122, 37JJ0123, 37KI1300, 37KI1301, 37LA0158, 37LA0159, 37LI0320, 37LI0322, 37LJ1522 and 3 more

Product

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

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0600-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.