FDASeptember 22, 2020device

ProVu Single Use Video Stylet with ET Tube, Part/Size: 038-990-080U/ 8.0, 038-990-075U/ 7.5, 038-990-070U/ 7.0, 038-990-065U/ 6.5 *Note: product list updated per 12/23/2020 letter to customers

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

The hazard

When the video stylet cuff is over-inflated there is potential for occlusion of the corrugated section of the ETT, and increased resistance to gas flow and difficulty in ventilating the patient.

What to do

FDA enforcement status: Terminated

Brands named

flexicare medicalflexicare

Recall history

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

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