FDANovember 27, 2019device

BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2, CE 0120, Do not Re-use, Rx Only, REF: 040-342U, Sterile EO, Qty 10, UDI: (01)15055788724053(17)230901(10)181002320

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

15055788724053

Recall history

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

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