FDADecember 15, 2017device

ARROW ENDURANCE" Extended Dwell Peripheral Catheter System, Catalog Numbers: EDC-00820 & EDC-00820-B

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

The hazard

Certain lots of peripheral catheter systems may be missing the safety latch, intended to minimize the risk of sharps injuries.

What to do

FDA enforcement status: Terminated

Brands named

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Recall history

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

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