Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported July 10, 2024
BD Pyxis, Name/REF: BD PYXIS MB TOWER MAIN/ 169-153, BD PYXIS MB TOWER MAIN CR/ 169-154, BD PYXIS MB TOWER MAIN W/MP/ 169-157, BD PYXIS MB TWR MN 1FM-10HH-1FH MP/ 169-143, BD PYXIS MB TWR MN 2FH-1FM-4HH-2FM MP/ 169-145, BD PYXIS MB TWR MN 2FM-8HH-1FH MP/ 169-144, BD PYXIS MB TWR MN 4FH-4HH-1FM MP/ 169-142, BD PYXIS MB TWR RXNOW MAIN W/MED PRINTER / 169-155, BD PYXIS MB TWR RXNOW MAIN W/PAT PRINTER/ 169-156, BD PYXIS MDBANK TWR MN 7HH-1HM-3FM/ 169-132, BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow/ 1
Multiple socket-outlet power strips that shipped with automated dispensing cabinet devices have not been certified to International Electrotechnical Commission (IEC) electrical st…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
CareFusion 303, Inc. recalled BD Pyxis, Name/REF: BD PYXIS MB TOWER MAIN/ 169-153, BD PYXIS MB TOWER MAIN CR/ 169-154,… - a moderate-severity action.
BD Pyxis, Name/REF: BD PYXIS MB TOWER MAIN/ 169-153, BD PYXIS MB TOWER MAIN CR/ 169-154,… was recalled by CareFusion 303, Inc. in July 10, 2024. Reason: Multiple socket-outlet power strips that shipped with automated dispensing cabinet devices have not been cert…. Check the official notice for the remedy. Verify recall #Z-2256-2024 with the FDA Devices before acting.
The recall
CareFusion 303, Inc. issued this moderate-severity FDA Devices recall-Multiple socket-outlet power strips that shipped with automated dispensing cabinet devices have not been cert….
- Moderate
- severity level
- 3K units
- affected scope
- Class II
- classification
- July 10, 2024
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2256-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2256-2024) was formally reported on July 10, 2024, with the manufacturer initiating the action on May 13, 2024. It is classified under Moderate severity (Class II), with a current status of Ongoing. CareFusion 303, Inc. is listed as the recalling firm, operating out of San Diego, CA. Federal records list the affected scope as 3002.
The documented reason for this recall is: Multiple socket-outlet power strips that shipped with automated dispensing cabinet devices have not been certified to International Electrotechnical Commission (IEC) electrical standards when used as a system with autom… Distribution data in the federal record shows the product reached: US Nationwide distribution including in the states of NY, CA, MO, AZ, CO, KS, IL, FL, OK, OH, TN, GA, NM, NV, NE, TX, NC, KY, WI, SC, IA, MT, SD, VA, NJ, PA, AK, MS, MI, WA, UT, ND, MA, MN, OR, IN, WV, AL, ID, LA, CT, W…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
3002
Related Recalls
6
3 from same agency
Product description
BD Pyxis, Name/REF: BD PYXIS MB TOWER MAIN/ 169-153, BD PYXIS MB TOWER MAIN CR/ 169-154, BD PYXIS MB TOWER MAIN W/MP/ 169-157, BD PYXIS MB TWR MN 1FM-10HH-1FH MP/ 169-143, BD PYXIS MB TWR MN 2FH-1FM-4HH-2FM MP/ 169-145, BD PYXIS MB TWR MN 2FM-8HH-1FH MP/ 169-144, BD PYXIS MB TWR MN 4FH-4HH-1FM MP/ 169-142, BD PYXIS MB TWR RXNOW MAIN W/MED PRINTER / 169-155, BD PYXIS MB TWR RXNOW MAIN W/PAT PRINTER/ 169-156, BD PYXIS MDBANK TWR MN 7HH-1HM-3FM/ 169-132, BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow/ 169-131, BD PYXIS MEDBANK TWR MN 10HH-1FH-1FM/ 169-23, BD PYXIS MEDBANK TWR MN 10HH-2FH/ 169-24, BD PYXIS MEDBANK TWR MN 10HH-2FM/ 169-25, BD PYXIS MEDBANK TWR MN 12HH-1FF/ 169-26, BD PYXIS MEDBANK TWR MN 12HH-1FH/ 169-27, BD PYXIS MEDBANK TWR MN 12HH-1FM/ 169-28, BD PYXIS MEDBANK TWR MN 14HH/ 169-29, BD PYXIS MEDBANK TWR MN 1FH-10HM-1FM/ 169-138, BD PYXIS MEDBANK TWR MN 1HH-1HM-2FM-4FF/ 169-30, BD PYXIS MEDBANK TWR MN 2FH-2HM-4FM/ 169-31, BD PYXIS MEDBANK TWR MN 2HH-10HM-1FM/ 169-32, BD PYXIS MEDBANK TWR MN 2HH-1FH-5FM/ 169-33, BD PYXIS MEDBANK TWR MN 2HH-2FH-4FM/ 169-34, BD PYXIS MEDBANK TWR MN 2HH-2FM-4FF/ 169-35, BD PYXIS MEDBANK TWR MN 2HH-4FH-2FM/ 169-139, BD PYXIS MEDBANK TWR MN 2HH-4HM-4FF/ 169-36, BD PYXIS MEDBANK TWR MN 2HH-4HM-4FM/ 169-37, BD PYXIS MEDBANK TWR MN 2HH-6FM/ 169-38, BD PYXIS MEDBANK TWR MN 2HH-6HM-3FM/ 169-39, BD PYXIS MEDBANK TWR MN 2HH-8HM-2FM/ 169-40, BD PYXIS MEDBANK TWR MN 2HM-6FM/ 169-41, BD PYXIS MEDBANK TWR MN 3FH-4FM/ 169-42, BD PYXIS MEDBANK TWR MN 3FH-8HH MEDPASS/ 169-140, BD PYXIS MEDBANK TWR MN 3HH-7HM-2FM/ 169-43, BD PYXIS MEDBANK TWR MN 4HH-10HM/ 169-44, BD PYXIS MEDBANK TWR MN 4HH-1FH-2HM-3FM/ 169-45, BD PYXIS MEDBANK TWR MN 4HH-1FH-4FM/ 169-46, BD PYXIS MEDBANK TWR MN 4HH-1FH-4HM-2FM/ 169-47, BD PYXIS MEDBANK TWR MN 4HH-1FH-6HM-1FM/ 169-48, BD PYXIS MEDBANK TWR MN 4HH-2FH-2HM-2FM/ 169-49, BD PYXIS MEDBANK TWR MN 4HH-2FH-3FM/ 169-50, BD PYXIS MEDBANK TWR MN 4HH-2HM-4FM/ 169-51, BD PYXIS MEDBANK TWR MN 4HH-3FH-2FM/ 169-52, BD PYXIS MEDBANK TWR MN 4HH-4FH-1FM/ 169-53, BD PYXIS MEDBANK TWR MN 4HH-4HM-3FM/ 169-54, BD PYXIS MEDBANK TWR MN 4HH-5FH / 169-55, BD PYXIS MEDBANK TWR MN 4HH-5FM/ 169-56, BD PYXIS MEDBANK TWR MN 4HH-6HM-2FM/ 169-57, BD PYXIS MEDBANK TWR MN 4HH-8HM-1FM/ 169-58, BD PYXIS MEDBANK TWR MN 4HM-5FM/ 169-59, BD PYXIS MEDBANK TWR MN 5HH-3HM-3FM/ 169-60, BD PYXIS MEDBANK TWR MN 5HH-9HM/ 169-61, BD PYXIS MEDBANK TWR MN 6FH-1FM/ 169-62, BD PYXIS MEDBANK TWR MN 6HH-1FH-2HM-2FM/ 169-63, BD PYXIS MEDBANK TWR MN 6HH-1FH-3FM/ 169-64, BD PYXIS MEDBANK TWR MN 6HH-2FH-2FM/ 169-65, BD PYXIS MEDBANK TWR MN 6HH-2FH-2HM-1FM/ 169-66, BD PYXIS MEDBANK TWR MN 6HH-4FH / 169-67, BD PYXIS MEDBANK TWR MN 6HH-4FM/ 169-68, BD PYXIS MEDBANK TWR MN 6HH-4HM-2FM/ 169-69, BD PYXIS MEDBANK TWR MN 6HH-6HM-1FM/ 169-70, BD PYXIS MEDBANK TWR MN 6HH-8HM/ 169-71, BD PYXIS MEDBANK TWR MN 7FH/ 169-72, BD PYXIS MEDBANK TWR MN 7FM/ 169-73, BD PYXIS MEDBANK TWR MN 7HH-1HM-3FM/ 169-74, BD PYXIS MEDBANK TWR MN 8HH-1FH-2FM/ 169-75, BD PYXIS MEDBANK TWR MN 8HH-1FH-2HM-1FM/ 169-76, BD PYXIS MEDBANK TWR MN 8HH-2FH-1FM/ 169-77, BD PYXIS MEDBANK TWR MN 8HH-2HM-2FM/ 169-78, BD PYXIS MEDBANK TWR MN 8HH-3FF/ 169-79, BD PYXIS MEDBANK TWR MN 8HH-3FH/ 169-80, BD PYXIS MEDBANK TWR MN 8HH-3FM/ 169-81, BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P/ 169-82, BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P/ 169-83, BD PYXIS MEDBANK TWR MN CR-12HH-1FH/ 169-84, BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P/ 169-85, BD PYXIS MEDBANK TWR MN CR-14HH-P/ 169-86, BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM/ 169-87, BD PYXIS MEDBANK TWR MN CR-2HH-6FH/ 169-88, BD PYXIS MEDBANK TWR MN CR-2HH-6FM/ 169-89, BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P/ 169-90, BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P/ 169-91, BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P/ 169-92, BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P/ 169-93, BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P/ 169-94, BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P/ 169-95, BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P/ 169-96, BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P/ 169-97, BD
Reason for recall
Multiple socket-outlet power strips that shipped with automated dispensing cabinet devices have not been certified to International Electrotechnical Commission (IEC) electrical standards when used as a system with automated dispensing cabinet devices, so use may expose user to leakage currents that could cause varying degrees of harm from a minor shock to permanent impairment.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-2256-2024 |
| Date reported | July 10, 2024 |
| Date initiated | May 13, 2024 |
| Recalling firm | CareFusion 303, Inc. |
| Firm location | San Diego, CA |
| Affected scope | 3002 |
| Distribution | US Nationwide distribution including in the states of NY, CA, MO, AZ, CO, KS, IL, FL, OK, OH, TN, GA, NM, NV, NE, TX, NC, KY, WI, SC, IA, MT, SD, VA, NJ, PA, AK, MS, MI, WA, UT, ND, MA, MN, OR, IN, WV, AL, ID, LA, CT, WY, MD, NH, AR, HI, D… |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2256-2024) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
BD Pyxis, Name/REF: BD PYXIS MB TOWER MAIN/ 169-153, BD PYXIS MB TOWER MAIN CR/ 169-154, BD PYXIS MB TOWER MAIN W/MP/ 169-157, BD PYXIS MB TWR MN 1FM-10HH-1FH MP/ 169-143, BD PYXIS MB TWR MN 2FH-1FM-4HH-2FM MP/ 169-145, BD PYXIS MB TWR MN 2FM-8HH-1FH MP/ 169-144, BD PYXIS MB TWR MN 4FH-4HH-1FM MP/ 169-142, BD PYXIS MB TWR RXNOW MAIN W/MED PRINTER / 169-155, BD PYXIS MB TWR RXNOW MAIN W/PAT PRINTER/ 169-156, BD PYXIS MDBANK TWR MN 7HH-1HM-3FM/ 169-132, BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow/ 169-131, BD PYXIS MEDBANK TWR MN 10HH-1FH-1FM/ 169-23, BD PYXIS MEDBANK TWR MN 10HH-2FH/ 169-24, BD PYXIS MEDBANK TWR MN 10HH-2FM/ 169-25, BD PYXIS MEDBANK TWR MN 12HH-1FF/ 169-26, BD PYXIS MEDBANK TWR MN 12HH-1FH/ 169-27, BD PYXIS MEDBANK TWR MN 12HH-1FM/ 169-28, BD PYXIS MEDBANK TWR MN 14HH/ 169-29, BD PYXIS MEDBANK TWR MN 1FH-10HM-1FM/ 169-138, BD PYXIS MEDBANK TWR MN 1HH-1HM-2FM-4FF/ 169-30, BD PYXIS MEDBANK TWR MN 2FH-2HM-4FM/ 169-31, BD PYXIS MEDBANK TWR MN 2HH-10HM-1FM/ 169-32, BD PYXIS MEDBANK TWR MN 2HH-1FH-5FM/ 169-33, BD PYXIS MEDBANK TWR MN 2HH-2FH-4FM/ 169-34, BD PYXIS MEDBANK TWR MN 2HH-2FM-4FF/ 169-35, BD PYXIS MEDBANK TWR MN 2HH-4FH-2FM/ 169-139, BD PYXIS MEDBANK TWR MN 2HH-4HM-4FF/ 169-36, BD PYXIS MEDBANK TWR MN 2HH-4HM-4FM/ 169-37, BD PYXIS MEDBANK TWR MN 2HH-6FM/ 169-38, BD PYXIS MEDBANK TWR MN 2HH-6HM-3FM/ 169-39, BD PYXIS MEDBANK TWR MN 2HH-8HM-2FM/ 169-40, BD PYXIS MEDBANK TWR MN 2HM-6FM/ 169-41, BD PYXIS MEDBANK TWR MN 3FH-4FM/ 169-42, BD PYXIS MEDBANK TWR MN 3FH-8HH MEDPASS/ 169-140, BD PYXIS MEDBANK TWR MN 3HH-7HM-2FM/ 169-43, BD PYXIS MEDBANK TWR MN 4HH-10HM/ 169-44, BD PYXIS MEDBANK TWR MN 4HH-1FH-2HM-3FM/ 169-45, BD PYXIS MEDBANK TWR MN 4HH-1FH-4FM/ 169-46, BD PYXIS MEDBANK TWR MN 4HH-1FH-4HM-2FM/ 169-47, BD PYXIS MEDBANK TWR MN 4HH-1FH-6HM-1FM/ 169-48, BD PYXIS MEDBANK TWR MN 4HH-2FH-2HM-2FM/ 169-49, BD PYXIS MEDBANK TWR MN 4HH-2FH-3FM/ 169-50, BD PYXIS MEDBANK TWR MN 4HH-2HM-4FM/ 169-51, BD PYXIS MEDBANK TWR MN 4HH-3FH-2FM/ 169-52, BD PYXIS MEDBANK TWR MN 4HH-4FH-1FM/ 169-53, BD PYXIS MEDBANK TWR MN 4HH-4HM-3FM/ 169-54, BD PYXIS MEDBANK TWR MN 4HH-5FH / 169-55, BD PYXIS MEDBANK TWR MN 4HH-5FM/ 169-56, BD PYXIS MEDBANK TWR MN 4HH-6HM-2FM/ 169-57, BD PYXIS MEDBANK TWR MN 4HH-8HM-1FM/ 169-58, BD PYXIS MEDBANK TWR MN 4HM-5FM/ 169-59, BD PYXIS MEDBANK TWR MN 5HH-3HM-3FM/ 169-60, BD PYXIS MEDBANK TWR MN 5HH-9HM/ 169-61, BD PYXIS MEDBANK TWR MN 6FH-1FM/ 169-62, BD PYXIS MEDBANK TWR MN 6HH-1FH-2HM-2FM/ 169-63, BD PYXIS MEDBANK TWR MN 6HH-1FH-3FM/ 169-64, BD PYXIS MEDBANK TWR MN 6HH-2FH-2FM/ 169-65, BD PYXIS MEDBANK TWR MN 6HH-2FH-2HM-1FM/ 169-66, BD PYXIS MEDBANK TWR MN 6HH-4FH / 169-67, BD PYXIS MEDBANK TWR MN 6HH-4FM/ 169-68, BD PYXIS MEDBANK TWR MN 6HH-4HM-2FM/ 169-69, BD PYXIS MEDBANK TWR MN 6HH-6HM-1FM/ 169-70, BD PYXIS MEDBANK TWR MN 6HH-8HM/ 169-71, BD PYXIS MEDBANK TWR MN 7FH/ 169-72, BD PYXIS MEDBANK TWR MN 7FM/ 169-73, BD PYXIS MEDBANK TWR MN 7HH-1HM-3FM/ 169-74, BD PYXIS MEDBANK TWR MN 8HH-1FH-2FM/ 169-75, BD PYXIS MEDBANK TWR MN 8HH-1FH-2HM-1FM/ 169-76, BD PYXIS MEDBANK TWR MN 8HH-2FH-1FM/ 169-77, BD PYXIS MEDBANK TWR MN 8HH-2HM-2FM/ 169-78, BD PYXIS MEDBANK TWR MN 8HH-3FF/ 169-79, BD PYXIS MEDBANK TWR MN 8HH-3FH/ 169-80, BD PYXIS MEDBANK TWR MN 8HH-3FM/ 169-81, BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P/ 169-82, BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P/ 169-83, BD PYXIS MEDBANK TWR MN CR-12HH-1FH/ 169-84, BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P/ 169-85, BD PYXIS MEDBANK TWR MN CR-14HH-P/ 169-86, BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM/ 169-87, BD PYXIS MEDBANK TWR MN CR-2HH-6FH/ 169-88, BD PYXIS MEDBANK TWR MN CR-2HH-6FM/ 169-89, BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P/ 169-90, BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P/ 169-91, BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P/ 169-92, BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P/ 169-93, BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P/ 169-94, BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P/ 169-95, BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P/ 169-96, BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P/ 169-97, BD. Recalled by CareFusion 303, Inc.. Units affected: 3002.
Why was this product recalled? ▼
Multiple socket-outlet power strips that shipped with automated dispensing cabinet devices have not been certified to International Electrotechnical Commission (IEC) electrical standards when used as a system with automated dispensing cabinet devices, so use may expose user to leakage currents that could cause varying degrees of harm from a minor shock to permanent impairment.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 10, 2024. Severity: Moderate. Recall number: Z-2256-2024.
Where was the recalled product distributed? ▼
Distribution: US Nationwide distribution including in the states of NY, CA, MO, AZ, CO, KS, IL, FL, OK, OH, TN, GA, NM, NV, NE, TX, NC, KY, WI, SC, IA, MT, SD, VA, NJ, PA, AK, MS, MI, WA, UT, ND, MA, MN, OR, IN, WV, AL, ID, LA, CT, WY, MD, NH, AR, HI, DC..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2256-2024) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported July 10, 2024. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.