CareFusion Alaris Syringe Module 811: Dim LED Display May Affect Readings
CareFusion recalls Alaris Syringe Module Model 8110 for potential dim LED display that could lead to inaccurate infusion monitoring. Affected units have specific serial numbers.
Lower-risk recall
LED display, which provides infusion or patient monitoring values, on the module may have segments that appear dim.
Contact the company
What happened, in plain English
CareFusion is recalling Alaris Syringe Module Model 8110 syringes because their LED display may appear dim, potentially causing inaccurate infusion monitoring. This could matter for healthcare workers using the device to program infusion settings. Read more at govinfonow.com/recall/64875-carefusion-alaris-syringe-module-811-dim-led-display-may-affect.
Source Summary by GovInfoNow · govinfonow.com/recall/64875-carefusion-alaris-syringe-module-811-dim-led-display-may-affect · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2823-2020
Cite this page
“CareFusion Alaris Syringe Module 811: Dim LED Display May Affect Readings.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/64875-carefusion-alaris-syringe-module-811-dim-led-display-may-affect. Based on FDA recall #Z-2823-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2823-2020%22&limit=1).
Why it’s dangerous
The LED display on the module may show dim segments, which could lead to inaccurate readings of infusion or patient monitoring values. This might cause healthcare workers to misinterpret the device's status during programming.
Who’s affected
Healthcare caregivers using the Alaris Syringe Module Model 8110 for infusion programming are most at risk. The recall affects specific serial numbers of the device.
How to tell if you have this one
Check the serial number on the Alaris Syringe Module Model 8110. The product is intended for trained healthcare caregivers to automate infusion programming.
- Brand
CareFusion- Category
Medical device
All 5 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 II- Status
Ongoing- Distribution
Worldwide distribution - U.S. Nationwide distribution including in the states of CO, FL, SC, NY, CA, NC, TX, IL, PA, AZ, LA, IN, MA, MO, AR, WI, HI, OR, OH, NJ, TN, NE, WA, KS, MI, MD, WV, KY, UT, MN, IA, GA, AL, DE, AK, VA, OK, NM, CT, SD, NV, ID, MT, ME, VT, MS, WY, NH, MP, DC, ND, GU, PR, AS, RI and the countries of TR, QA, CA, AE, KW, MX, GI, IL, SA, CH, NL, BE, TW, ZA, PH, CN, AU, IN, FR, MY, NZ, GB, KR, PK, DE, SG, JP, CU, IT, BH.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-2822-2020 | Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual steps necessary to enter infusion data.; All serial numbers | 1442097 |
| Z-2823-2020 | Alaris Syringe Module Model 8110 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual steps necessary to enter infusion data.; All serial numbers | 130612 |
| Z-2824-2020 | Alaris PCA Module Model 8120 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual steps necessary to enter infusion data.; All serial numbers | 89497 |
| Z-2825-2020 | Alaris EtCO2 Module Model 8300 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual steps necessary to enter infusion data.; All serial numbers | 40671 |
| Z-2826-2020 | Alaris SpO2 Module Model 8210 and Model 8220 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual steps necessary to enter infusion data.; All serial numbers | 8558 |
What to do — step by step
Check Serial Number
Identify the serial number on the Alaris Syringe Module Model 8110 to confirm if it is affected.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 50 states.
FDA distribution: “Worldwide distribution - U.S. Nationwide distribution including in the states of CO, FL, SC, NY, CA, NC, TX, IL, PA, AZ, LA, IN, MA, MO, AR, WI, HI, OR, OH, NJ, TN, NE, WA, KS, MI, MD, WV, KY, UT, MN, IA, GA, AL, DE, AK, VA, OK, NM, CT,…” 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, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA published this recall 57 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- 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-2823-2020 (June 30, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2823-2020 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.