FDADecember 8, 2020device

smiths medical portex Loss of Resistance Device, REF 100/398/000

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

The hazard

The labeling was missing information on sterilization and prohibition of reuse.

What to do

FDA enforcement status: Terminated

Brands named

smiths medical asdsmithssmiths medical

Recall history

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

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