FDAJanuary 21, 2022device

1. Footrest ( use exclusively in combination with Intelli-C devices) 2. Shoulder support ( use exclusively in combination with Intelli-C devices)

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

The hazard

Friction rubber block in the clamping mechanism was missing in the Footrest. It may slip down along the patient table while in use with a patient. This accessory is designed to use with Intelli-C, Right and Intelli-C, Left.

What to do

FDA enforcement status: Ongoing

Brands named

nrt x ray a snrt

UPCs

057134640003369032820000469032820000579032820000759032820000070903282000001903282000002903282000004903282000006903282000009903282000011903282000016

Recall history

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

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