FDAMarch 19, 2021device

Protek Solo Venous Dilator Set: dilator, vessel, for percutaneous catheterization. Catalog #: 5840-2417 - LS Tandem Life Kit - V24/A17 Catalog #: 5840-2415 - LS Tandem Life Kit - V24/A15 Catalog #: 5740-2417 - TandemLife Kit - V24/A17 Catalog #: 5100-1422 - ProtekSolo Venous Dilator Set (14-22 Fr)

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

On 02/26/2021, it was found that there were incorrectly packaged Dilator sets in Finished Goods. On 03/1/2021, it was confirmed that 14 kits containing the impacted products had been distributed to the field.

What to do

FDA enforcement status: Terminated

Brands named

cardiac assistcardiac

UPCs

00814112020463008141120205170081411202070800814112020092

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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