Source: FDA | Recall date: 05/20/2026
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Affected 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
Summary: Due to nonconforming products being inadvertently distributed.
Hazard: Due to nonconforming products being inadvertently distributed.
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