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Stryker Corporation recalls Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to
Recalled May 20, 2026 · FDA recall Z-2166-2026 · Stryker
Hazard
Due to nonconforming products being inadvertently distributed. · FDA Class II
Units
10 tube sets
Sold at
U.S. Nationwide distribution in the state of GA.
Description
Due to nonconforming products being inadvertently distributed.
Product
Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to be used with the FluidSmart Fluid Management System, which is intended for irrigation and fluid warming in laparoscopic procedures, and distention, fluid warming, and volume/deficit measurements in endoscopic procedures within gynecology, urology, and orthopedic disciplines.
Manufacturer(s)
Stryker Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →