BD Pyxis MedStation ES recall
BD Pyxis MedStation ES REF: 323 Medication cabinet
Why was BD Pyxis MedStation ES recalled?
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All Serial Numbers/UDI:10885403512667
- Product
- BD Pyxis MedStation ES REF: 323 Medication cabinet
- Recalling firm
- CareFusion 303, Inc.
- Quantity
- 15,933
- Distribution
- US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
- Recall date
- June 10, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)