BD Pyxis MedStation ES (Med ES Main), REF 323
Reported: January 29, 2025 Initiated: February 14, 2023 #Z-0971-2025
Product Description
BD Pyxis MedStation ES (Med ES Main), REF 323
Reason for Recall
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
Details
- Recalling Firm
- CareFusion 303, Inc.
- Units Affected
- 94466 units
- Distribution
- Worldwide
- Location
- San Diego, CA
Frequently Asked Questions
What product was recalled? ▼
BD Pyxis MedStation ES (Med ES Main), REF 323. Recalled by CareFusion 303, Inc.. Units affected: 94466 units.
Why was this product recalled? ▼
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 29, 2025. Severity: Moderate. Recall number: Z-0971-2025.
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