FDA Medical devices recall ·
BD Pyxis MedBank Mini recall
- Recall number
- Z-2304-2026
- Date
- (initiated April 30, 2026)
- Company / brand
- CareFusion 303, Inc.
10020 Pacific Mesa Blvd, San Diego, CA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 114 units
- Hazard tags
- Burn
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
Why was it recalled?
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
All Serial Numbers/UDI:10885403517181
Distribution
US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
States: California Massachusetts
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2304-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.