FDAOctober 29, 2020device

PryTime Medical - ER-Reboa Plus Catheter, Ref: ER7232PLUS, Guidewire Free, Compatabel with 7Fr introducer Sheaths, Arterial Line, Rx Only, UDI: (01) 0 0850001 10505 7 - Product Usage: intended for temporary occlusion of large vessels and blood pressure monitoring including patients requiring emer...

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

The hazard

There is a potential that catheters may have incorrectly marked balloon and arterial lines. This could result in a procedure delay or injury to the patient.

What to do

FDA enforcement status: Terminated

Brands named

prytime medical devicesprytimeprytime medical

UPCs

00850001105057

Recall history

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

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