Baxter Infusion Pump Recall: Battery Issues from Prolonged Storage
Baxter Healthcare recalls specific infusion pumps with battery codes 35083, 35162, 35195, 35724, 35223, and 36010 due to battery performance issues from prolonged storage.
Lower-risk recall
Battery performance issues related to prolonged storage.
Contact the company
What happened, in plain English
Baxter Healthcare is recalling certain infusion pumps that may have battery performance issues if stored for long periods. This could lead to improper function of the pump, which is critical for medical use. Read more at govinfonow.com/recall/63466-baxter-infusion-pump-recall-battery-issues-from-prolonged-storage.
Source Summary by GovInfoNow · govinfonow.com/recall/63466-baxter-infusion-pump-recall-battery-issues-from-prolonged-storage · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1150-2021
Cite this page
“Baxter Infusion Pump Recall: Battery Issues from Prolonged Storage.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/63466-baxter-infusion-pump-recall-battery-issues-from-prolonged-storage. Based on FDA recall #Z-1150-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1150-2021%22&limit=1).
Why it’s dangerous
The battery in these pumps may not perform correctly after prolonged storage, potentially causing the pump to malfunction. This could affect the delivery of medication or fluids to patients, which is critical for medical treatment.
Who’s affected
Patients using Baxter infusion pumps with specific product or battery codes listed in the recall are affected. Healthcare providers and patients who use these pumps for medical treatments are at risk if the pump malfunctions due to battery issues.
How to tell if you have this one
Check the product code on the pump (35700ABB, 35700BAX, 35700BAX2, 3570009) or battery code (35083, 35162, 35195, 35724, 35223, 36010) to see if it matches the recalled items.
- Brand
Baxter Healthcare- Category
Medical device
What to do — step by step
Check Product Code
Look for product codes 35700ABB, 35700BAX, 35700BAX2, or 3570009 on the pump.
Check Battery Code
Check for battery codes 35083, 35162, 35195, 35724, 35223, or 36010 on the battery.
Where it went and when
Where it was distributed
Distributed in 50 states and D.C. and Puerto Rico, and outside the U.S.
FDA distribution: “Domestic Distribution: ST, AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: 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 terminated this recall 5.3 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Do I need to stop using the pump immediately?
No, the recall does not require immediate stop use; however, you should check the product and battery codes to ensure it is affected.
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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-1150-2021 (January 6, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1150-2021 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.