Cardinal Health Monoject 1 mL Syringes May Not Work With Infusion Pumps
Cardinal Health recalls 1 mL Tuberculin Syringes with Luer-Lock Tips due to compatibility issues with infusion pumps. Affected units include specific lot numbers from 2019-2023.
Use caution until it’s fixed
Demonstrated recognition and compatibility issues with syringe infusion pumps.
Contact the company
What happened, in plain English
Cardinal Health is recalling 1 mL Tuberculin Syringes with Luer-Lock Tips because they may not work properly with infusion pumps. This could lead to incorrect dosing or treatment errors if used with certain medical devices. Read more at govinfonow.com/recall/57296-cardinal-health-monoject-1-ml-syringes-may-not-work-with.
Source Summary by GovInfoNow · govinfonow.com/recall/57296-cardinal-health-monoject-1-ml-syringes-may-not-work-with · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0145-2024
Cite this page
“Cardinal Health Monoject 1 mL Syringes May Not Work With Infusion Pumps.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57296-cardinal-health-monoject-1-ml-syringes-may-not-work-with. Based on FDA recall #Z-0145-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0145-2024%22&limit=1).
Why it’s dangerous
The syringes may not recognize or interact correctly with infusion pumps, which could cause incorrect dosing or treatment errors. This might lead to unsafe medication delivery if the pump fails to function properly.
Who’s affected
People using these syringes for medical treatments, especially those with infusion pumps. Patients who have recently received the recalled syringes are most at risk.
How to tell if you have this one
Check the product code 1180100777 on the syringe packaging. Look for lot numbers 221201 through 230601 on the box or case. These syringes were sold between 2019 and 2023.
- Brand
Cardinal Health- Category
Medical device
All 6 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Ongoing- Distribution
US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-0145-2024 | Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack; Product Code: 1180100777; UDI/DI: 10192253034530 - each, 20192253034537 - box, 50192253034538 - case; Lot Numbers: 221201, 221202, 221203, 230201, 230202, 230203, 230204, 230205, 230601 | 3,113,846 units |
| Z-0146-2024 | Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack; Product Code: 1180600777; UDI/DI: 10192253034608 - each, 20192253034605 - box, 50192253034606 - case; Lot Numbers: 221201, 221202, 221203, 221204, 221205, 230201, 230202, 230203, 230204, 230205, 230206, 230207 | 3,936,682 units |
| Z-0147-2024 | Monoject" 12 mL Syringe Luer-Lock Tip Soft Pack; Product Code: 1181200777T; UDI/DI: 10192253025811 - each, 20192253025818 - box, 50192253025819 - case; Lot Numbers: 221101, 221102, 221103, 221104 | 3,084,300 units |
| Z-0148-2024 | Monoject 20 mL Syringe Luer-Lock Tip Soft Pack; Product Code: 1182000777; UDI/DI: 10192253034677 - each, 20192253034674 - box, 50192253034675 - case; Lot Numbers: 221201, 221202, 221203, 221204, 221205, 230201, 230202, 230203, 230204, 230205, 230206 | 4,913,520 units |
| Z-0149-2024 | Monoject" 35 mL Syringe Luer-Lock Tip Soft Pack; Product Code: 1183500777; UDI/DI: 10192253034691 - each, 20192253034698 - box, 50192253034699 - case; Lot Numbers: 221201, 230201, 230601, 230602 | 1,097,048 units |
| Z-0150-2024 | Monoject" 60 mL Syringe Luer-Lock Tip Soft Pack; Product Code: 1186000777T; UDI/DI: 10192253025835 - each, 20192253025832 - box, 50192253025833 - case; Lot Numbers: 221101, 230601 | 457,200 units |
What to do — step by step
Check Product Details
Verify the product code (1180100777) and lot numbers (221201-230601) on the syringe packaging.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 44 states.
FDA distribution: “US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA published this recall 42 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0145-2024 (September 20, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0145-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.