FDANovember 30, 2015device

Medrad Source Administration Sets, Catalog number INT CSS. For use with MEDRAD Intego PET Infusion pump Systems, in nuclear medicine diagnostic procedures.

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

The hazard

The firm's investigation of the Medrad Intego indicates that the inner diameter of the saline tubing is out of specification and may result in the system failing to position the dose correctly during extraction, potentially leading to a low measurement of the extracted dose or to a higher dose being extracted. The occluded SAS tubing may impair the priming function and prompt an RP prime fail

What to do

FDA enforcement status: Terminated

Brands named

bayer healthcarebayer

Recall history

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

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