Thermedx FluidSmart Urology Tube Set recall
Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to be used with the FluidSmart Fluid…
Why was Thermedx FluidSmart Urology Tube Set recalled?
Due to nonconforming products being inadvertently distributed.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Catalog Number: LL0006 UDI-DI code: 00860936000365 Lot Number: B000576601
- 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…
- Recalling firm
- Stryker Corporation
- Quantity
- 10 tube sets
- Distribution
- U.S. Nationwide distribution in the state of GA.
- Recall date
- May 20, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)