FDAApril 5, 2023device

BD Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation ES (Med ES Main Tower), REF: 352; BD Pyxis Anesthesia Station ES, REF: 327; BD Pyxis CII Safe ES Tower Main, REF: 1116-00; BD Pyxis CII Safe ES, Desktop PC, W-LESS SCNR, BIO, REF: 107-255-01

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

The hazard

Automated dispensing cabinet software is experiencing: 1) ES device download failure resulting in partial patient information loss that leads to 2) partial loss of patient transaction data, seen as a server upload processing error. Outdated/incorrect information display may contribute to the removal of medication to which the patient is allergic, incorrect dose amount, or discontinued medication.

What to do

FDA enforcement status: Ongoing

Brands named

carefusion 303carefusion

UPCs

10885403512667108854035126741088540347783610885403512605

Recall history

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

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