Fresh Recalls

BD Pyxis MedBank Tower REF: recall status

Notice names this product. CareFusion 303’s BD Pyxis MedBank Tower REF is named in FDA Class II recall Z-2303-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Fingerprint scanner may overheat to a temperature to cause 1st degree burn. Identifying details: All Serial Numbers/UDI:10885403517167. Units affected: 607 units. Status: Ongoing.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
BD Pyxis MedBank Tower REF
Company / brand
CareFusion 303
Lot / serial / date codes
All Serial Numbers/UDI:10885403517167
Distribution
US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
Agency product description and boundaries

BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

Brand
CareFusion 303

Recalls naming this model

FDA Class II · Medical device · June 10, 2026

BD Pyxis MedBank Tower REF recall — CareFusion 303, Inc.

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

Company / brand: CareFusion 303 recalls

Affected product: BD Pyxis MedBank Tower REF recall status

Official ID Z-2303-2026 · Official record ↗

See all CareFusion 303 recalls →

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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.