fda_recall · device_recall · high

Stryker Corporation — Class II recall: Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365…

Event date
2026-05-20 00:00:00Z
Observed
2026-07-09 22:52:29Z
Source ID
Z-2166-2026
Payload hash
7ce0373107818613fdb6a0ae

Summary

Due to nonconforming products being inadvertently distributed. Status: Ongoing.

Informational only. Not legal, financial, or medical advice.