FDANovember 27, 2019device

BriteBlade Pro Single-Use Fiber Optic Mac 3, CE01120, Do Not Re-use, Rx Only, REF 040-713U, Sterile EO, Qty 10, (01)15055788723001 The device is intended for direct vision laryngoscopy to obtain an illuminated view of the vocal cords and the glottis by insertion into the oral cavity to manipulate...

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

The hazard

The firm has received reports that the spring/washer/bearing components in the block of the laryngoscope blade become loose and separated from the device. If the blade is disengage over the patient's mount it is a possibility that any loose parts could enter the oral cavity which could cause a delay in the procedure while retrieving loose parts.

What to do

FDA enforcement status: Terminated

Brands named

flexicare medicalflexicare

UPCs

15055788723001

Recall history

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

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