Recall Z-2297-2026— CareFusion 303, Inc.
Class II · Ongoing
Class II FDA medical device recall by CareFusion 303, Inc., initiated 2026-04-30. FDA's recall record names no specific 510(k) clearance for this event. Product: BD Pyxis MedStation 4000 REF: 303 Medication cabinet. Reason: Fingerprint scanner may overheat to a temperature to cause 1st degree burn..
- Recalling firm
- CareFusion 303, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-04-30
- Firm location
- San Diego, CA, United States
Product description
BD Pyxis MedStation 4000 REF: 303 Medication cabinet
Reason for recall
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Data sourced from openFDA. This site is unofficial and independent of the FDA.