FDAClass II · Medical device · Recall Z-2301-2026 · Recalled June 10, 2026

BD Pyxis Mini Main REF recall — CareFusion 303, Inc.

Agency report date: June 10, 2026.

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 Mini Main REF
Company / brand: CareFusion 303
Lot / serial / date codes: All Serial Numbers/UDI:10885403512582
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 Mini Main REF: 349 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.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: BD Pyxis Mini Main REF recall status

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2301-2026
Brand: All CareFusion 303 recalls
Classification: Class II
Units affected: 709 units
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

BD Pyxis Mini Main REF recall status

Companies & origin

Recalling firm location: San Diego, CA, United States
Firm address: 10020 Pacific Mesa Blvd, 92121-4386

Identifying details (verbatim from the notice)

Product codes / lots: All Serial Numbers/UDI:10885403512582
Distribution: US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
Firm notified the public via: Letter
FDA event ID: 98895
Recall initiated: April 30, 2026
FDA classified: June 3, 2026
FDA report date: June 10, 2026

Other medical device recalls from around the same time

Giraffe Warmer with Integrated Resuscitation System (iRes) recall — Datex-Ohmeda IncFDA · June 24, 2026
Giraffe Stand-alone Infant Resuscitation System recall — Datex-Ohmeda IncFDA · June 24, 2026
Design Options Spinal Tray Spinal Needle Anesthesia procedure kits recall — B Braun Medical IncFDA · June 10, 2026
Spinocan Spinal Needle procedure kits recall — B Braun Medical IncFDA · June 10, 2026
Spinal Needle procedure kits recall — B Braun Medical IncFDA · June 10, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved September 8, 2026 at 6:00 PM UTC.

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