FDAOctober 6, 2022device

Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP 120803FP 120404FP 120804FP 120805FP 120806FP 120807FP Fogarty Arterial Embolectomy Catheter with Stylet Model Number: 120403FSP 120803FSP

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

The hazard

Due to an increase of confirmed latex deterioration complaints for arterial embolectomy catheters packaged in pouches.

What to do

FDA enforcement status: Ongoing

Brands named

edwards lifesciencesedwards

UPCs

00690103205206006901032050840069010320509100690103205107006901032052130069010320522000690103205237006901032017890069010320519000690103205244

Recall history

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

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