BD Pyxis MedBank MedPass Software recall: Software Issue
BD Pyxis MedBank MedPass Software, REF: 139088-01
Why was BD Pyxis MedBank MedPass Software recalled?
After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is still available for dispense, which could lead to duplicate medication administration.
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?
UDI-DI: 10885403513817, Software versions prior to but not including v1.2.3.23
- Product
- BD Pyxis MedBank MedPass Software, REF: 139088-01
- Recalling firm
- CareFusion 303, Inc.
- Quantity
- 37
- Distribution
- US: FL, MI, KS
- Recall date
- October 4, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)