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CareFusion 303, Inc. 2026-06-10 Health serious FDA
Health · FDA · Recall #FDA-Z-2303-2026

BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet Recall

Issued June 10, 2026 · CareFusion 303, Inc.

In June 2026, CareFusion 303, Inc. recalled the BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

What you should do

  1. 1 Stop using BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact CareFusion 303, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
CareFusion 303, Inc.
Category
Health
Recall date
June 10, 2026
Units affected
Not reported
Sold at
US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
Recall number
FDA-Z-2303-2026
Made in
United States
Issuing agency
FDA

In context

  • CareFusion 303, Inc. has 13 recalls in our database, including 1 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 356th Health recall we've logged in 2026.
Read the official FDA notice

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