CareFusion 303, Inc. recalls BD Pyxis Mini Main REF: 349 Medication cabinet

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

On April 30, 2026, CareFusion (subsidiary of Becton, Dickinson and Company) issued a Urgent Medical Device Recall Notification, via mail or Email. CareFusion ask consignees to take the following actions: 1. Dispensing cabinets can continue to be used as intended. 2. If you suspect that the Bio-ID Scanner is hot, please discontinue the use of Scanner and file a complaint. 3. Review and update facility policies and procedures related to situations where the Bio-ID Scanner is unavailable to mitigate delays in care. 4. Complete the attached Customer Response Form and return to the BD contact noted on the form.

• FDA enforcement recordOfficial FDA database entry for Z-2301-2026
• FDA device classification · BRYOfficial FDA classification for this device type
• CFR regulation · 21 CFR 868.6100The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find CareFusion 303, Inc.Search for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.