FDA Device recall Z-2486-2024
BD PYXIS MEDBANK MINI CR-4HH-P, REF: 169-115 containing software version 3.9.1.9
- FDA Device
- Class II
- ongoing
- Published 2024-08-14
On 2024-08-14 the FDA classified a Class II recall of BD PYXIS MEDBANK MINI CR-4HH-P, REF: 169-115 containing software version 3.9.1.9 by Carefusion 303, citing due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2486-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-06-24 |
| Published | 2024-08-14 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
BD PYXIS MEDBANK MINI CR-4HH-P, REF: 169-115 containing software version 3.9.1.9
Reason
Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
Identifiers
| code_info | UDI: 10885403512544/ Serial Number: 16170661 16210908 16089019 16062433 16147169 16080412 16124906 15940375 15940373 1…UDI: 10885403512544/ Serial Number: 16170661 16210908 16089019 16062433 16147169 16080412 16124906 15940375 15940373 15940374 15940376 15957620 15957621 15941307 15967410 15967412 15967409 15967413 15967411 15967361 15943774 16056924 16188928 15943781 15943470 15943782 15872417 15902417 15902418 15888968 15253736 15253737 16247094 16283979 16225069 16222611 16165533 16205727 16270832 16200474 16244810 16250223 15935617 15654707 15654706 15489245 15723803 15927979 15924532 15569608 15832680 15832679 15824206 15815815 15815825 15415136 15415135 15415137 15415138 15622987 16174396 16193269 15939084 15939085 15854218 15854728 15854727 15398915 15383489 15489244 15489243 15606150 15606167 15924529 15888948 15924530 15924528 15569630 15575989 15575996 15575979 15575978 15575988 15575986 15575985 15569629 15575975 15587203 15587204 15587205 15824205 15824210 15824221 15815826 15815830 15852349 15852348 15353925 15353926 15422146 15422154 15422152 15422155 15422153 15422149 15422148 15422151 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2486-2024%22
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