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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 95070

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
July 09, 2024
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
CareFusion 303, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

BD Pyxis QFill Replenishment Station, REF: 138904-01, medication cabinet system

Z-2947-2024
Recall number
Z-2947-2024
Initiated
July 09, 2024
Classification
Class II
Status
Ongoing
Recalling firm
CareFusion 303, Inc.
Quantity
3 units

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
software issue

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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.

Code information

serial numbers: 44210411, 43880801, 44227426/ UDI: None

Distribution pattern

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

device · product 2 of 2

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

Z-2948-2024
Recall number
Z-2948-2024
Initiated
July 09, 2024
Classification
Class II
Status
Ongoing
Recalling firm
CareFusion 303, Inc.
Quantity
Unavailable

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
software issue

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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.

Code information

serial numbers: 16056243 16068264 16082950 16142772 16192674 16208218 16208219 16284106 16346254 16388826 16388833 16623139 / UDI: None

Distribution pattern

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