FDA recall record

CareFusion 303 BKIT BD Pyxis QFill Replenishment Station, REF: 155197-01, medication cabinet recall — FDA Z-2948-2024

Due to software issue, there is a potential when a restock label is printed for a medication stored in a non-CUBIE location, that the incorrect bin for…

Class IIclassification
Z-2948-2024official record ID
Sep 11, 2024report date

Recall record at a glance

Official recordZ-2948-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCareFusion 303, Inc.
Report dateSep 11, 2024
Recall initiation dateJul 9, 2024
LocationSan Diego, CA, United States

Official product description

BKIT BD Pyxis QFill Replenishment Station, REF: 155197-01, medication cabinet system

Why the product was recalled

Due to software issue, there is a potential when a restock label is printed for a medication stored in a non-CUBIE location, that the incorrect bin for the medication is printed on the label.

Distribution information

US Nationwide distribution in the states of CA, FL, KS, MN, NJ, NY, PA.

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: not stated.

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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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