BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower
Medical device recall Z-1930-2024. Published in FDA’s Enforcement Report on Jun 5, 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 Jun 5, 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 53 states named
- 35,029 units 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?
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower, REF: 306
35,029 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
UDI: 10885403512636/Serial Numbers added 8/27/2025: 12558525 13351845 15616389 15616390 15616391 15563540 15544135 15544136 15544137 15544138 15544139 15406818 15358663 15067079 15067087 15067090 15067097 15067101 15067102 15067106…
Every code shown here, 1,990 characters
UDI: 10885403512636/Serial Numbers added 8/27/2025: 12558525 13351845 15616389 15616390 15616391 15563540 15544135 15544136 15544137 15544138 15544139 15406818 15358663 15067079 15067087 15067090 15067097 15067101 15067102 15067106 15067107 14785182 14785183 14785184 14785185 14689030 14689031 14689033 14671361 14671362 14671363 14671364 14671365 14671366 14671367 14671369 14671370 14659569 14659570 14659571 14659572 14659573 14659574 14659576 14659577 14659578 14639957 14637299 14637300 14637301 14637302 14637303 14637304 14633430 14633431 14633432 14633433 14633434 14633435 14633436 14607306 14607307 14607308 14607309 14607310 14607311 14607312 14607313 14607314 14590696 14590697 14590698 14590699 14590700 14590702 14590703 14578551 14578552 14578553 14578554 14578555 14578556 14578558 14578559 14565988 14565989 14565990 14565991 14565992 14565993 14565994 14565995 14565996 14565997 14598309 15777264 15570731 15110842 14906229 14906231 14906233 14906235 14906237 14906238 14724865 14724866 14724867 14724868 14724869 14724870 14724871 14724872 14724873 14724875 14724876 14724877 14724878 14147868 14895210 14895212 8000132477 8000132478 12458388 12453585 14771237 14771238 13419887 13419888 14054009 13720803 13720812 13720815 13720817 13720829 13720832 13720836 13720839 13720841 13720843 13720847 13720850 13720854 13720863 13720866 13720871 13720878 13720880 13720882 13720884 13720888 13720893 13720894 13720899 13720902 13720908 13668699 13668700 13668701 13662199 13647263 13647264 13838583 8000090022 8000090023 8000091120 8000091121 8000091122 8000091124 8000091125 8000091126 8000094985 8000094987 8000094988 12794937 8000054590 13218022 13024432 13840570 13839433 15107217 15107218 15107219 15024443 13701499 15770171 15107202 15107203 15107204 15107206 15107207 15107208 15107209 15107210 15107211 15107212 15107216 15107221 15107222 15107223 15107224 15107225 15107226 15107227 15024445 15024446 15024447 15024448 15024449 14629650 12719020 14373401 8000037077…
FDA’s list runs to 348,603 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 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, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and the countries of South Africa, Kuwait, Qatar, Singapore, Bermuda, United Arab Emirates, Argentina, Australia, Belgium, Bahrain, Brazil, Bahamas, Canada, Chile, China, Germany, Spain, Finland, France, United Kingdom, Greece, Hong Kong, Ireland, Italy, Japan, South Korea, Lebanon, Morocco, Mexico, New Zealand, Oman, Portugal, Thailand, Taiwan.
The states and territories these words name
53 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
- 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 Apr 15, 2024.
- FDA classified it on May 30, 2024.
- FDA’s Enforcement Report published it on Jun 5, 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.
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 348,603 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
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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.