Drug recall
BD Pyxis MedBank System - Product Label/labeling pending
FDA recall event 91099 · Class II · CareFusion 303, Inc.
Key facts
| Event ID | 91099 |
|---|---|
| Recall numbers | Z-0928-2023 |
| Recalling firm | CareFusion 303, Inc. |
| Product type | Devices |
| Products | BD Pyxis MedBank System - Product Label/labeling pending |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Due to customer complaints related to the MedBank software which may indicate that a different medication is loaded in a cubie (drawer) pocket than what is physically loaded and listed on the pocket… |
| Initiation date | Dec 12, 2022 |
| Report date | Jan 18, 2023 |
| City | San Diego |
| State | CA |
| Country | United States |
| FEI number | 2016493 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: