Various models of BD Pyxis Medbank: Reference numbers: 1137-00 1145-00 1146-00 1147-00 1148-00
Pending LLM rewrite. Source: FDA_DEVICE Z-0367-2026.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
The recalled product
- Product
- Various models of BD Pyxis Medbank: Reference numbers: 1137-00 1145-00 1146-00 1147-00 1148-00 138902-01 138903-01 138905-01 138906-01 138907-01 138908-01 138909-01 138910-01 138911-01 138912-01 138913-01 138914-01 138915-01 138916-01 138917-01 138918-01 13
- Manufacturer
- CareFusion 303, Inc.
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- All Serial Numbers/Ref #/UDI: 1137-00 N/A
- 1145-00 10885403517167
- 1146-00 10885403517174
- 1147-00 10885403517181
- 1148-00 10885403517198
- 138902-01 N/A
- 138903-01 N/A
- 138905-01 N/A
- 138906-01 N/A
- 138907-01 N/A
- 138908-01 N/A
- 138909-01 N/A
- 138910-01 N/A
- 138911-01 N/A
- 138912-01 N/A
- 138913-01 N/A
- 138914-01 N/A
- 138915-01 N/A
- 138916-01 N/A
- 138917-01 N/A
Distribution
Distributed nationwide across the United States.
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