Reported Apr 30, 2025 · Ongoing
BD PYXIS MEDBANK (Name, REF)
CareFusion 303, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: CareFusion 303, Inc. · 10020 Pacific Mesa Blvd · San Diego, CA · 92121-4386
Is this the product you have?
BD PYXIS MEDBANK (Name, REF)
105 of 105 products
| # | Product as published |
|---|---|
| 1 | MEDPASS MODULE, 139088-01 |
| 2 | MINI 1FH-1FM, 169-137 |
| 3 | MINI 1HH-1FH-1HM, 169-101 |
| 4 | MINI 1HH-1HM-1FM, 169-102 |
| 5 | MINI 2FH, 138902-01 |
| 6 | MINI 2FH, 169-104 |
| 7 | MINI 2FM, 169-105 |
| 8 | MINI 2HH-1FH, 169-106 |
| 9 | MINI 2HH-1FH, 138908-01 |
| 10 | MINI 2HH-1FM, 169-107 |
| 11 | MINI 2HH-1FM, 138906-01 |
| 12 | MINI 3HH-1FG, 169-110 |
| 13 | MINI 3HH-1FG, 139091-01 |
| 14 | MINI 3HH-1HM, 169-111 |
| 15 | MINI 4HH, 138910-01 |
| 16 | MINI 4HH, 169-112 |
| 17 | MINI 4HM, 169-113 |
| 18 | MINI 4HM, 138915-01 |
| 19 | TWR MN 10HH-1FH-1FM, 169-23 |
| 20 | TWR MN 10HH-2FH, 169-24 |
- Lot codes and dates
- REF/UDI-DI(GTIN)/Software Version
108 of 108 codes
139088-01/1.2.3.23169-137/10885403512544/2.4169-101/10885403512544/2.4169-102/10885403512544/2.4138902-01/2.4169-104/10885403512544/2.4169-105/10885403512544/2.4169-106/10885403512544/2.4138908-01/2.4169-107/10885403512544/2.4138906-01/2.4169-108/10885403512544/2.4169-110/10885403512544/2.4139091-01/2.4169-111/10885403512544/2.4138910-01/2.4169-112/10885403512544/2.4169-113/10885403512544/2.4138915-01/2.4169-23/10885403512568/2.4169-24/10885403512568/2.4138955-01/2.4169-25/10885403512568/2.4138924-01/2.4169-26/10885403512568/2.4138960-01/2.4169-27/10885403512568/2.4138961-01/2.4169-28/10885403512568/2.4138926-01/2.4138927-01/2.4169-29/10885403512568/2.4169-30/10885403512568/2.4169-31/10885403512568/2.4169-32/10885403512568/2.4169-33/10885403512568/2.4169-34/10885403512568/2.4169-139/10885403512568/2.4139125-01/2.4169-38/10885403512568/2.4138919-01/2.4169-39/10885403512568/2.4169-40/10885403512568/2.4169-41/10885403512568/2.4169-42/10885403512568/2.4138933-01/2.4169-140/10885403512568/1.2.3.23169-43/10885403512568/2.4169-44/10885403512568/2.4138959-01/2.4169-45/10885403512568/2.4169-46/10885403512568/2.4169-47/10885403512568/2.4169-49/10885403512568/2.4169-50/10885403512568/2.4138931-01/2.4169-52/10885403512568/2.4169-53/10885403512568/2.4138940-01/2.4169-54/10885403512568/2.4
- REF/UDI-DI(GTIN)/Software Version
- Amount recalled
- 7,357
Where it was sold
Why it was recalled
Users trying to restock a single bin location of an automated dispensing cabinet, during pocket exchange restocking workflow, may experience a software issue that results in 2 destock transactions and 2 stock transactions, which results in doubling the bin quantity, which may result in a delay in access to desired medications and/or supplies, which may lead to temporary body function impairment.
This product could cause temporary or reversible health problems — stop using it.
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