FDA Device recall Z-1230-2025
139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK MINI 1FH-2HH MEDPASS 169-152 BD PYXIS MEDBANK MINI 2HH-1FM MEDPASS 169-1…
- FDA Device
- Class II
- ongoing
- Published 2025-03-05
On 2025-03-05 the FDA classified a Class II recall of 139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK MINI 1FH-2HH MEDPASS 169-152 BD PYXIS MEDBANK MINI 2HH-1FM MEDPASS 169-1… by Carefusion 303, citing labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1230-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-01-08 |
| Published | 2025-03-05 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK MINI 1FH-2HH MEDPASS 169-152 BD PYXIS MEDBANK MINI 2HH-1FM MEDPASS 169-150 BD PYXIS MEDBANK MINI 4HH MEDPASS 169-140 BD PYXIS MEDBANK TWR MN 3FH-8HH MEDPASS
Reason
Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.
Identifiers
| code_info | MEDFLEX 1119-00 10885403512704 MEDFLEX 2.0 1139-00 10885403512704 MEDBANK TOWER MAIN 1145-00 10885403517167 MEDBANK MIN…MEDFLEX 1119-00 10885403512704 MEDFLEX 2.0 1139-00 10885403512704 MEDBANK TOWER MAIN 1145-00 10885403517167 MEDBANK MINI MAIN 1147-00 10885403517181 BD PYXIS MEDBANK MINI 2FH 138902-01 N/A BD PYXIS MEDBANK MINI 2FM 138903-01 N/A BD Pyxis MedBank Twr Mn 4HH-8HM-1FM 138905-01 N/A BD PYXIS MEDBANK MINI 2HH-1FM 138906-01 N/A BD PYXIS MEDBANK MINI 2HH-2HM 138907-01 N/A BD PYXIS MEDBANK MINI 2HH-1FH 138908-01 N/A BD PYXIS MEDBANK MINI 3HH-1HM 138909-01 N/A BD PYXIS MEDBANK MINI 4HH 138910-01 N/A BD PYXIS MEDBANK MINI CR-4HH-P 138911-01 N/A BD PYXIS MEDBANK MINI 1HH-3HM 138912-01 N/A BD PYXIS MEDBANK MINI CR-2HH-1FH-P 138913-01 N/A BD Pyxis MedBank Twr Mn 5HH-9HM 138914-01 N/A BD PYXIS MEDBANK MINI 4HM 138915-01 N/A BD PYXIS MEDBANK TWR MN 4HM-5FM 138916-01 N/A BD PYXIS MEDBANK TWR MN 4HH-5FH 138917-01 N/A BD PYXIS MEDBANK TWR MN 4HH-5FM 138918-01 N/A BD PYXIS MEDBANK TWR MN 2HH-6FM 138919-01 N/A BD PYXIS MEDBANK TWR MN 7FH 138920-01 N/A BD PYXIS MEDBANK MINI 1HH-1FH-1HM 138921-01 N/A BD PYXI |
|---|
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-1230-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.