Recall Z-1207-2025— CareFusion 303, Inc.
Class II · Ongoing
Class II FDA medical device recall by CareFusion 303, Inc., initiated 2025-01-23. FDA's recall record names no specific 510(k) clearance for this event. Product: BD Pyxis MedFlex 2.0 REF 1139-00 Bio-ID Spare Parts REF 353200-01 The BD Pyxis" MedFlex is an Automated Dispensing Cabinet (ADC) intended to securely store and dispense medications and supplies to a qualified and authorized user in a clinical setting.. Reason: Due to fingerprint scanner failing resulting in the scanner heating up..
- Recalling firm
- CareFusion 303, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-01-23
- Firm location
- San Diego, CA, United States
Product description
BD Pyxis MedFlex 2.0 REF 1139-00 Bio-ID Spare Parts REF 353200-01 The BD Pyxis" MedFlex is an Automated Dispensing Cabinet (ADC) intended to securely store and dispense medications and supplies to a qualified and authorized user in a clinical setting.
Reason for recall
Due to fingerprint scanner failing resulting in the scanner heating up.
Data sourced from openFDA. This site is unofficial and independent of the FDA.