Notice names this product. CareFusion 303’s BD Pyxis MedStation ES Tower REF is named in FDA Class II recall Z-2302-2026. 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:10885403512674. Units affected: 465 units. Status: Ongoing.
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.
BD Pyxis MedStation ES Tower REF: 352 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.
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Affected product: BD Pyxis MedStation ES Tower REF recall status
Official ID Z-2302-2026 · Official record ↗
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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.