BD Pyxis MedStation ES 7 Drawer Auxiliary Tower
Medical device recall Z-0671-2025. Published in FDA’s Enforcement Report on Dec 18, 2024.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Dec 18, 2024. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word, and 54 states named
- 40,763 how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is 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.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Due to a software issue, automated dispensing cabinet devices may open the wrong cubie pocket or position, which can lead to: 1) Unintended and incorrect medication removal, or 2) Potential for a different medication (medication pulled in error) to be refilled/loaded, which may lead to may lead to low inventory or a stockout.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
BD Pyxis MedStation ES 7 Drawer Auxiliary Tower, REF: 324
40,763, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
All software versions. REF/UDI-DI: 324/10885403512681/ 12440840 12440841 12448208 12452252 12452264 12455476 12462734 12462735 12463676 12468609 12468612 12468607 12468608 12468610 12468671 12468672 12468674 12468670 12468673 12468611…
Every code shown here, 1,999 characters
All software versions. REF/UDI-DI: 324/10885403512681/ 12440840 12440841 12448208 12452252 12452264 12455476 12462734 12462735 12463676 12468609 12468612 12468607 12468608 12468610 12468671 12468672 12468674 12468670 12468673 12468611 12474015 12474022 12473810 12473813 12473815 12473816 12473817 12473811 12473921 12474012 12474071 12474014 12473887 12473922 12474013 12473807 12473812 12473808 12473809 12476548 12495456 12499285 12502858 12502857 12503069 12508589 12508584 12508578 12508579 12508587 12508580 12510555 12510559 12510393 12520264 12520266 12520267 12520269 12528519 12528411 12530586 12530588 12530589 12530587 12531133 12531132 12532495 12532494 12532490 12532491 12532493 12532492 12533583 12533588 12533589 12533562 12533563 12533561 12533584 12533587 12533585 12533586 12533259 12533261 12533262 12533263 12534455 12534456 12534461 12540265 12540264 12544944 12546962 12547840 12547841 12549213 12552380 12552381 12553970 12553971 12553972 12553973 12553558 12553773 12553559 12553974 12553766 12553767 12553774 12555796 12555818 12555808 12555807 12563092 12563091 12563094 12564425 12568586 12568682 12572289 12572290 12572295 12572296 12572301 12572304 12572294 12572306 12572308 12572297 12572298 12572292 12572299 12572300 12572305 12572302 12572307 12572904 12572907 12572908 12572900 12572901 12572902 12572905 12572906 12572903 12575531 12579325 12582556 12582557 12583764 12583765 12583766 12583762 12583767 12583769 12583770 12583761 12583768 12583771 12586361 12588457 12588462 12588460 12588475 12588658 12588657 12588466 12588467 12589599 12589594 12589602 12589597 12589601 12589603 12589604 12589679 12589655 12589654 12589915 12591607 12591608 12591604 12591609 12591605 12591606 12592584 12593277 12593278 12593881 12593841 12593842 12594535 12594534 12595267 12596860 12596873 12596861 12598571 12598573 12598572 12599172 12599173 12599175 12599171 12599176 12599177 12600360 12600361 12599975 12600650 12600801 12600800 12600804 12600805 12600803 12604313…
FDA’s list runs to 367,558 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide - US Nationwide distribution including in the states of OK, LA, FL, AR, VA, KY, PA, AL, NC, CA, MN, AK, TX, MI, ME, OH, OR, NY, IL, RI, GA, WI, NH, KS, CO, WA, MO, MD, AZ, SC, NV, WV, NM, IN, NJ, TN, DE, MT, MA, VT, DC, NE, CT, ID, WY, MS, UT, HI, IA, SD, ND, GU, MP, PR and the countries of CA, BR, JP, ES, NZ, AU, FR, AR, MX, IT, CL, TR, SA, MY, CH, IE, TH, SG, KW, BE, DE, PT, QA, MA, FI, AE, EG, BS, GB, BM, GR, BH, KR, MC, PL, LB, HK, IN, IL, MO, IQ, TN, NO, PH, CO, TW, CN, JO, OM.
The states and territories these words name
54 states and territories.
Every one of them
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- District of Columbia
- Delaware
- Florida
- Georgia
- Guam
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Northern Mariana Islands
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Puerto Rico
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Nov 14, 2024.
- FDA classified it on Dec 11, 2024.
- FDA’s Enforcement Report published it on Dec 18, 2024.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- CareFusion 303, Inc., of San Diego, CA.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 367,558 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.