FDADecember 9, 2022device

CADD Administration Set, List Numbers: a) REF 21-7346-24; b) REF 21-7363-24

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

The hazard

There are two potential issues with CADD Infusion System Infusion Sets: (1) Lack of Delivery or Underdelivery related to Tubing Occlusion and (2) False "No Disposable Attached (NDA)" Alarms

What to do

FDA enforcement status: Ongoing

Brands named

smiths medical asdsmithssmiths medical

UPCs

350195171619573501951716196

Recall history

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

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