BD Pyxis MedBank Tower Medication Cabinet Recall
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CareFusion 303, Inc. is recalling 607 units of the BD Pyxis MedBank Tower medication cabinet due to a fingerprint scanner that may overheat and cause first-degree burns.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 10, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, MedicalDevices.
What Happened CareFusion 303, Inc. initiated a voluntary recall of the BD Pyxis MedBank Tower medication cabinet after determining that the fingerprint scanner may overheat to a temperature that could cause a first-degree burn.
Which Products Are Affected The recall covers the BD Pyxis MedBank Tower, REF: 1145-00, Medication cabinet. All serial numbers are affected, with UDI 10885403517167. A total of 607 units are involved. Distribution was nationwide in the United States and to AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, and TW. The recall number is Z-2303-2026 and the classification is Class II.
What You Should Do Consumers should follow guidance from the recalling firm regarding the affected devices.
Why This Matters The recall addresses a potential burn hazard associated with the fingerprint scanner on the medication cabinet.
Source FDA recall Z-2303-2026, CareFusion 303, Inc., San Diego, CA.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (966 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to July 10, 2026.
Frequently Asked Questions
Common questions about this FDA recall.