Device recall: BD Pyxis MedStation ES, REF: 323, Medication Cabinet
Class II FDA enforcement event 94527. Recall start date: . Status in the FDA record: Ongoing.
Reason for recall, in the words of FDA
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
CareFusion 303, Inc. started this device recall on 15 Apr 2024. The firm address in the FDA record is in San Diego, CA. FDA put the recall in Class II. FDA event 94527 has 6 product records. The first FDA enforcement report date is 5 Jun 2024. The record gives the status Ongoing.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MP, MS, MT, NC, ND, NE, NH,…
Recalling firm
CareFusion 303, Inc., San Diego, CA.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
6 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-1927-2024 | BD Pyxis MedStation ES, REF: 323, Medication Cabinet | 212,367 units | Class II | Ongoing | 5 Jun 2024 |
| Z-1928-2024 | BD Pyxis MedStation 4000 System, REF: 303, Medication Cabinet | 91,933 units | Class II | Ongoing | 5 Jun 2024 |
| Z-1929-2024 | BD Pyxis" MedStation ES 7-Drawer Auxiliary Tower, REF: 324 | 87,302 units | Class II | Ongoing | 5 Jun 2024 |
| Z-1930-2024 | BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower, REF: 306 | 35,029 units | Class II | Ongoing | 5 Jun 2024 |
| Z-1931-2024 | BD Pyxis" Anesthesia Station ES, REF: 327 | 71,569 units | Class II | Ongoing | 5 Jun 2024 |
| Z-1932-2024 | BD Pyxis(TM) Anesthesia Station 4000, REF: 338 | 11,875 units | Class II | Ongoing | 5 Jun 2024 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2024
- 970
- Share of these events in Class II
- 87%
- Product records in this event
- 6Median of the firm: 1
- Events of the firm on the register
- 99
Other events of the firm
Official channels
- FDA enforcement report Z-1927-2024The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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Cite this page
Recall Register. FDA enforcement event 94527. https://recallregister.com/fda/ii/94527/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MP, MS, MT, NC, ND, NE, NH,…
- What quantity of product is in FDA event 94527?
- The event has 6 product records. The first record gives this quantity:
212,367 units
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2024 have the same class?
- 87% of the 970 device events that started in 2024 are in Class II.