BD 60-In Extension Sets: Risk of Inadequate Sterilization
BD recalls 60-inch non-DEHP minibore extension sets with UDI-DI codes 10885403236235, 10885403274619, and 10885403237218 due to potential inadequate sterilization processing.
Lower-risk recall
Products may not have received adequate sterilization processing.
What happened, in plain English
BD is recalling 60-inch non-DEHP minibore extension sets that may not have been properly sterilized. This could lead to infections or other health risks if used in medical procedures. Read more at govinfonow.com/recall/459506-bd-60-in-extension-sets-risk-of-inadequate-sterilization.
Source Summary by GovInfoNow · govinfonow.com/recall/459506-bd-60-in-extension-sets-risk-of-inadequate-sterilization · Updated August 27, 2026 · FDA enforcement record: FDA #Z-2941-2026
Cite this page
“BD 60-In Extension Sets: Risk of Inadequate Sterilization.” GovInfoNow, updated August 27, 2026. https://govinfonow.com/recall/459506-bd-60-in-extension-sets-risk-of-inadequate-sterilization. Based on FDA recall #Z-2941-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2941-2026%22&limit=1).
Why it’s dangerous
The sets may not have received adequate sterilization, which could result in contamination and infection if used in medical procedures. This is a potential risk during intravenous fluid administration.
Who’s affected
Healthcare professionals and patients using these sets for intravenous fluid administration. Those with the specific UDI-DI codes listed are most at risk.
How to tell if you have this one
Check for the UDI-DI codes: 10885403236235, 10885403274619, or 10885403237218. These sets are used for intravenous fluid administration and were sold with specific lot numbers.
- Brand
BD- Category
Medical device
What to do — step by step
Check Product Codes
Look for the UDI-DI codes listed: 10885403236235, 10885403274619, or 10885403237218 on the packaging or product.
Where it went and when
Where it was distributed
Distributed in 26 states, and outside the U.S.
FDA distribution: “U.S.: AZ, CA, CO, FL, GA, IL, IN, KS, MD, MI, MN, MO, MS, NC, NV, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA O.U.S.: Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Colorado, Florida, Georgia, Illinois, Indiana, Kansas, Maryland, Michigan, Minnesota, Mississippi, Missouri, Nevada, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Dakota, Tennessee, Texas, Utah, Virginia, Washington.
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
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-2941-2026 (June 16, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2941-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 27, 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.