Becton Dickinson recalls BD SmartSite Filter Extension Sets that contain di(2-ethylhexyl) phthalate (DEHP) instead of being DEHP-free. These sets may pose health risks during medical use.
Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).
Becton Dickinson is recalling certain BD SmartSite Filter Extension Sets because they contain DEHP (a phthalate chemical) instead of being DEHP-free as labeled. This could pose health risks during medical use, especially for patients receiving intravenous treatments.
These infusion sets were labeled as DEHP-free but actually contain di(2-ethylhexyl) phthalate (DEHP). DEHP is a chemical that can be harmful to health, particularly in medical settings where patients receive intravenous treatments.
Patients using these extension sets for intravenous treatments are most at risk. Healthcare providers who use these sets in medical settings may also be affected.
Look for BD SmartSite Filter Extension Sets with catalog numbers 10013902, 20062E, 70000N-07, ME1224, 20350ET, or 70001B-07T. The sets were sold from the manufacturer's production date through October 16, 2026.
Identify the catalog number on the product label to confirm if it is one of the recalled numbers: 10013902, 20062E, 70000N-07, ME1224, 20350ET, or 70001B-07T.
Reach out to Becton Dickinson directly for further assistance or to confirm if your product is affected.
These sets were labeled as DEHP-free but actually contain di(2-ethylhexyl) phthalate (DEHP), which can be harmful during medical use.
Check the product catalog number to see if it is one of the recalled numbers. Contact Becton Dickinson for further assistance.
Yes, patients receiving intravenous treatments using these sets may be at risk due to the presence of DEHP.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-0351-2024 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-0351-2024 from Becton Dickinson. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
