FDA recall record

CareFusion 303 BD Pyxis MedStation ES AUX, REF 324 recall — FDA Z-0972-2025

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…

Class IIclassification
Z-0972-2025official record ID
Jan 29, 2025report date

Recall record at a glance

Official recordZ-0972-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCareFusion 303, Inc.
Report dateJan 29, 2025
Recall initiation dateFeb 14, 2023
Quantity39615 units
LocationSan Diego, CA, United States

Official product description

BD Pyxis MedStation ES AUX, REF 324

Why the product was recalled

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,

Distribution information

Worldwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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