FDADecember 9, 2022device

CADD Administration Set, List Numbers: 1) REF 21-7300-24, 2) REF 21-7301-24 3) REF 21-7302-24, 4) REF 21-7321-24, 5) REF 21-7322-24, 6) REF 21-7323-24, 7) REF 21-7324-24, 8) REF 21-7333-24, 9) REF 21-7336-24, 10) REF 21-7339-24, 11) REF 21-7343-24, 12) REF 21-7349-24, 13) REF 21-7359-24, 14) REF ...

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

3061058602719630610586027219306105860272333061058602963330610586029640061058603961306105860296573061058604323330610586027295306105860273013501951719182435019517184239

Recall history

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

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CADD Administration Set, List Numbers: 1) REF 21-7300-24, 2) REF 21-7301-24 3) REF 21-7302-24, 4) REF 21-7321-24, 5) REF 21-7322-24, 6) REF 21-7323-24, 7) REF 21-7324-24, 8) REF 21-7333-24, 9) REF 21-7336-24, 10) REF 21-7339-24, 11) REF 21-7343-24, 12) REF 21-7349-24, 13) REF 21-7359-24, 14) REF ... — Recall Details · AllClear