Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported March 5, 2025
138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 138911-01 BD PYXIS MEDBANK MINI CR-4HH-P 169-115 BD PYXIS MEDBANK MINI CR-4HH-P 139001-01 BD PYXIS MEDBANK MN 200 CR-2HH-1FH-P 139002-01 BD PYXIS MEDBANK MN 200 CR-2HH-1FM-P 139000-01 BD PYXIS MEDBANK MN 200 CR-4HH-P 139020-01 BD PYXIS MEDBANK MN 500 CR-2HH-1FM-2DD-P 139018-01 BD PYXIS MEDBANK MN 500 CR-2HH-5FM-P 139019-01 BD PYXIS MEDBANK MN 500 CR-4HH-1FH-3FM-P 139021-01 BD PYXIS MEDBANK MN 500 CR-4HH-4FM-P
Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
CareFusion 303, Inc. recalled 138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 1… - a moderate-severity action.
138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 1… was recalled by CareFusion 303, Inc. in March 5, 2025. Reason: Labeling update to include a contraindication statement against the use of medicine cabinets in procedure an…. Check the official notice for the remedy. Verify recall #Z-1227-2025 with the FDA Devices before acting.
The recall
CareFusion 303, Inc. issued this moderate-severity FDA Devices recall-Labeling update to include a contraindication statement against the use of medicine cabinets in procedure an….
- Moderate
- severity level
- 6K units
- affected scope
- Class II
- classification
- March 5, 2025
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1227-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1227-2025) was formally reported on March 5, 2025, with the manufacturer initiating the action on January 8, 2025. 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 6,075 units.
The documented reason for this recall is: Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms. Distribution data in the federal record shows the product reached: US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX,…. 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
6,075 units
Related Recalls
6
3 from same agency
Product description
138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 138911-01 BD PYXIS MEDBANK MINI CR-4HH-P 169-115 BD PYXIS MEDBANK MINI CR-4HH-P 139001-01 BD PYXIS MEDBANK MN 200 CR-2HH-1FH-P 139002-01 BD PYXIS MEDBANK MN 200 CR-2HH-1FM-P 139000-01 BD PYXIS MEDBANK MN 200 CR-4HH-P 139020-01 BD PYXIS MEDBANK MN 500 CR-2HH-1FM-2DD-P 139018-01 BD PYXIS MEDBANK MN 500 CR-2HH-5FM-P 139019-01 BD PYXIS MEDBANK MN 500 CR-4HH-1FH-3FM-P 139021-01 BD PYXIS MEDBANK MN 500 CR-4HH-4FM-P 139022-01 BD PYXIS MEDBANK MN 500 CR-6HH-3FM-P 138973-01 BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P 155140-01 BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P 169-82 BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P 138975-01 BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P 155141-01 BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P 169-83 BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P 139073-01 BD PYXIS MEDBANK TWR MN CR-12HH-1FH 155142-01 BD PYXIS MEDBANK TWR MN CR-12HH-1FH 169-84 BD PYXIS MEDBANK TWR MN CR-12HH-1FH 138976-01 BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P 155143-01 BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P 169-85 BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P 138977-01 BD PYXIS MEDBANK TWR MN CR-14HH-P 155144-01 BD PYXIS MEDBANK TWR MN CR-14HH-P 169-86 BD PYXIS MEDBANK TWR MN CR-14HH-P 138951-01 BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM 155145-01 BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM 169-87 BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM 139072-01 BD PYXIS MEDBANK TWR MN CR-2HH-6FH 155146-01 BD PYXIS MEDBANK TWR MN CR-2HH-6FH 169-88 BD PYXIS MEDBANK TWR MN CR-2HH-6FH 139085-01 BD PYXIS MEDBANK TWR MN CR-2HH-6FM 155147-01 BD PYXIS MEDBANK TWR MN CR-2HH-6FM 169-89 BD PYXIS MEDBANK TWR MN CR-2HH-6FM 138968-01 BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P 155148-01 BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P 169-90 BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P 138964-01 BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P 155149-01 BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P 169-91 BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P 138966-01 BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P 155150-01 BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P 169-92 BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P 138967-01 BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P 155151-01 BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P 169-93 BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P 138969-01 BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P 155152-01 BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P 169-94 BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P 138965-01 BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P 155153-01 BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P 169-95 BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P 138971-01 BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P 155154-01 BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P 169-96 BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P 138972-01 BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P 155155-01 BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P 169-97 BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P 138974-01 BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P 155156-01 BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P 169-98 BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P 138970-01 BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P 155157-01 BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P 169-99 BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P
Reason for recall
Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-1227-2025 |
| Date reported | March 5, 2025 |
| Date initiated | January 8, 2025 |
| Recalling firm | CareFusion 303, Inc. |
| Firm location | San Diego, CA |
| Affected scope | 6,075 units |
| Distribution | US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI,… |
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-1227-2025) 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? ▼
138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 138911-01 BD PYXIS MEDBANK MINI CR-4HH-P 169-115 BD PYXIS MEDBANK MINI CR-4HH-P 139001-01 BD PYXIS MEDBANK MN 200 CR-2HH-1FH-P 139002-01 BD PYXIS MEDBANK MN 200 CR-2HH-1FM-P 139000-01 BD PYXIS MEDBANK MN 200 CR-4HH-P 139020-01 BD PYXIS MEDBANK MN 500 CR-2HH-1FM-2DD-P 139018-01 BD PYXIS MEDBANK MN 500 CR-2HH-5FM-P 139019-01 BD PYXIS MEDBANK MN 500 CR-4HH-1FH-3FM-P 139021-01 BD PYXIS MEDBANK MN 500 CR-4HH-4FM-P 139022-01 BD PYXIS MEDBANK MN 500 CR-6HH-3FM-P 138973-01 BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P 155140-01 BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P 169-82 BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P 138975-01 BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P 155141-01 BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P 169-83 BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P 139073-01 BD PYXIS MEDBANK TWR MN CR-12HH-1FH 155142-01 BD PYXIS MEDBANK TWR MN CR-12HH-1FH 169-84 BD PYXIS MEDBANK TWR MN CR-12HH-1FH 138976-01 BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P 155143-01 BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P 169-85 BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P 138977-01 BD PYXIS MEDBANK TWR MN CR-14HH-P 155144-01 BD PYXIS MEDBANK TWR MN CR-14HH-P 169-86 BD PYXIS MEDBANK TWR MN CR-14HH-P 138951-01 BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM 155145-01 BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM 169-87 BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM 139072-01 BD PYXIS MEDBANK TWR MN CR-2HH-6FH 155146-01 BD PYXIS MEDBANK TWR MN CR-2HH-6FH 169-88 BD PYXIS MEDBANK TWR MN CR-2HH-6FH 139085-01 BD PYXIS MEDBANK TWR MN CR-2HH-6FM 155147-01 BD PYXIS MEDBANK TWR MN CR-2HH-6FM 169-89 BD PYXIS MEDBANK TWR MN CR-2HH-6FM 138968-01 BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P 155148-01 BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P 169-90 BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P 138964-01 BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P 155149-01 BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P 169-91 BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P 138966-01 BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P 155150-01 BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P 169-92 BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P 138967-01 BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P 155151-01 BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P 169-93 BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P 138969-01 BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P 155152-01 BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P 169-94 BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P 138965-01 BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P 155153-01 BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P 169-95 BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P 138971-01 BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P 155154-01 BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P 169-96 BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P 138972-01 BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P 155155-01 BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P 169-97 BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P 138974-01 BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P 155156-01 BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P 169-98 BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P 138970-01 BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P 155157-01 BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P 169-99 BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P. Recalled by CareFusion 303, Inc.. Units affected: 6,075 units.
Why was this product recalled? ▼
Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 5, 2025. Severity: Moderate. Recall number: Z-1227-2025.
Where was the recalled product distributed? ▼
Distribution: US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1227-2025) 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 March 5, 2025. 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.