BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include
Medical device recall Z-1785-2022. Published in FDA’s Enforcement Report on Oct 5, 2022.
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 Oct 5, 2022. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word, and 43 states named
- 686 cabinets 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?
The automated dispensing cabinet software update included a .dll file that is not compatible with MedBank Cabinet stations with MedCart Matrix drawers. The cabinet system will stop functioning (Matrix drawers will stop opening in the MedBank Application) leading to delay in access to medications or supplies needed in residential or procedural care facilities.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex operating with Windows 7 . MedBank 200 Main operating with Windows 7 . MedBank 500 Main operating with Windows 7. An automated dispensing cabinet intended to securely store and dispense medications to health care providers in a clinical setting.
686 cabinets, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Software Version - v2.1.2.9 UDI Code: N/A Cabinet System Serial Numbers containing the affected software: 14473379 15268856 14728142 15080054 14891492 15216161 13819501 14443828 14443829 14443838 14461825 14461827 14461829 14461830…
Every code shown here, 1,996 characters
Software Version - v2.1.2.9 UDI Code: N/A Cabinet System Serial Numbers containing the affected software: 14473379 15268856 14728142 15080054 14891492 15216161 13819501 14443828 14443829 14443838 14461825 14461827 14461829 14461830 14461836 14461838 14461840 14461842 14461843 14461845 14461848 14473356 14473359 14473371 14473376 14473377 14491507 14491510 14491511 14491513 14491514 14491516 14491518 14491519 14491523 14491524 14491526 14491529 14491533 14491534 14491535 14491536 14491537 14509122 14509123 14509124 14509126 14509128 14509130 14509136 14509137 14509138 14509139 14509141 14531591 14532282 14532284 14532285 14532286 14532287 14532290 14532294 14532295 14532298 14532299 14532300 14532301 14532302 14568029 14568034 14568035 14568036 14568037 14568038 14568041 14568042 14568045 14568046 14568050 14568054 14603154 14607364 14607368 14607369 14649246 14699416 14532304 14568027 14461834 14491520 14491522 14532288 14532292 14532305 14491512 14532297 14443834 14532293 14532291 14607366 14443839 14443843 14443844 14460707 14603175 14607367 14461824 14443836 14509115 14509119 14549534 15279454 14699033 14730460 14420208 14730461 14549537 14730464 14473369 14699031 15125784 15317097 14723851 15274579 14442685 14568030 14568031 15633002 14730471 13770291 15590120 14478424 14874166 13947037 15361553 14509135 15071140 14138680 15537380 15615141 14728129 15788870 15286943 14478435 14491530 14715885 15429584 15337472 14721968 15564896 15564893 15564894 15564895 15513825 14624517 14861727 14861748 14961881 14961882 14961883 14961884 15830892 13945496 13945495 14697343 15581965 15774188 15366948 14813913 15089507 14947859 14403527 14229977 15317101 14175169 15581964 14649237 14228154 14728127 14159916 14406629 14429784 14699405 14607360 14443841 14443842 14586208 14649230 14649232 14403531 15188738 15575589 15267549 15700819 14509113 14478428 14478431 14874162 15294475 14540101 14304064 15366950 14443824 15267544 14427167 13843251 14813912 14709254 15229116 14951360…
FDA’s list runs to 6,279 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.
U.S. Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS,KY, LA, MA, MD, ME,. MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY.
The states and territories these words name
43 states and territories.
Every one of them
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Florida
- Georgia
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- Nebraska
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- 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.
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 May 24, 2022.
- FDA classified it on Sep 23, 2022.
- FDA’s Enforcement Report published it on Oct 5, 2022.
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 6,279 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.