[Recalled] BD Pyxis Med ES Auxiliary (AUX), REF 343 — Drawer and/or door failures that may lead to a delay in access to medications | FDA 2023-02-14
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | BD Pyxis Med ES Auxiliary (AUX), REF 343 |
|---|---|
| Brand / manufacturer | CareFusion 303, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0975-2025 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 14 February 2023 |
| EAN / barcode | 10885403512698 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from CareFusion 303, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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