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FDA DevicesClass II

BD Pyxis MedStation ES Tower REF: 352 Medication cabinet

Published: June 10, 2026Recall ID: Z-2302-2026Category: Medical DevicesCountry: United States
US
Medical DeviceFDA DevicesUSUS

BD Pyxis MedStation ES Tower REF: 352 Medication cabinet

Recalling Firm: CareFusion 303, Inc.

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Reason for Recall / Hazard

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

Product Description & Identification

BD Pyxis MedStation ES Tower REF: 352 Medication cabinet

Affected Products

BD Pyxis MedStation ES Tower REF: 352 Medication cabinet

Additional Source Details

FieldValue
CitySan Diego
StateCA
Event id98895
Address 110020 Pacific Mesa Blvd
Code infoAll Serial Numbers/UDI:10885403512674
Postal code92121-4386
Report date20260610
Product typeDevices
Product quantity465 units
Reason for recallFingerprint scanner may overheat to a temperature to cause 1st degree burn.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260430
Initial firm notificationLetter
Center classification date20260603

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Inspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.

2Isolate & Discontinue Use

Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Devices).

Your Legal Rights as a Consumer

Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.

Frequently Asked Questions About This Recall

FAQ Guide

Q1:What should I do immediately if I own or bought BD Pyxis MedStation ES Tower REF: 352 Medication cabinet?

Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.

Q2:Can I get a full refund or free repair for this recall?

Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.

Q3:Do I need my original sales receipt to claim a remedy or refund?

In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.

Q4:Where can I verify official information for this safety alert?

This safety alert is aggregated directly from official regulatory agency records (FDA Devices). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.

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Overview

  • Recalling FirmCareFusion 303, Inc.
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
Recall Hazard Severity
High Alert (Class I)
Official Agency Alert

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🚨 SAFETY ALERT: CareFusion 303, Inc. - BD Pyxis MedStation ES Tower REF: 352 Medication cabinet

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https://therecallfile.com/recalls/bd-pyxis-medstation-es-tower-ref-352-medication-cabinet/FDA-Z-2302-2026
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