FDAApril 29, 2021device

Adult-Pediatric Electrostatic Filter HME, Item Code 352/5877Z - Product Usage: indicated for single use on anesthetized patients and respiratory care patients who require a breathing circuit with ISO standard 15mm or 22 mm connectors.

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

The hazard

The company was notified by their supplier of sterilization services for airway products in Italy of potential deviations from validated parameters for ethylene oxide sterilization.

What to do

FDA enforcement status: Ongoing

Brands named

covidien lpcovidiencovidien lp

UPCs

1088452107740920884521077406

Recall history

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

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