FDAMay 12, 2020device

Type S Extension For use with Varian, CIVCO, Prescription Only - Product Usage: Device is intended for patient positioning.

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

The hazard

Potential for disengagement of the Varian Style Type-S Extension during patient repositioning. The risk associated with the disengagement of the extension could be a patient fall if the patient is not supported by clinical staff.

What to do

FDA enforcement status: Terminated

Brands named

med tecmed

UPCs

00841439104156

Recall history

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

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