BD recalls Alaris Pump infusion sets labeled as DEHP-free but actually contain di(2-ethylhexyl) phthalate (DEHP). Affected items have specific catalog numbers and were sold through medical suppliers. Contact BD for details.
Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).
BD is recalling certain Alaris Pump infusion sets that were labeled as free of DEHP but actually contain di(2-ethylhexyl) phthalate (DEHP). This chemical is a known endocrine disruptor that can cause health issues with long-term exposure, especially for patients receiving intravenous treatments.
The recalled infusion sets were labeled as DEHP-free but contain di(2-ethylhexyl) phthalate (DEHP), a chemical known to be an endocrine disruptor. Long-term exposure to DEHP can cause health issues, particularly for patients receiving intravenous treatments.
Patients using intravenous treatments with the recalled Alaris Pump infusion sets are most at risk. Healthcare providers who use these sets for medical treatments may also be affected.
Check for specific catalog numbers listed in the recall notice: 10010483, 10010453, 10010454, 10013072, 10013361, 10013890, 10015012, 10015862, 10062818, 10821753, 11171447, 11426964, 11532269, 11613191, 10015861A, 22000-B007T, 2202-0007, 2204-0007, 2206-0007, 2260-0500, 22600-0007T, 22601-B007T, 22602-B007T, 22603-B007T, 24001-0007, 2403-0007, 24301-0007T, 2441-0007, 2450-0500, 24600-0007, 24601-B007T, 2465-0007, 2466-0007. All lots with expiration dates through July 31, 2026.
Review the specific catalog numbers listed in the recall notice to determine if your infusion set is affected.
DEHP is a known endocrine disruptor that can cause health issues with long-term exposure, particularly for patients receiving intravenous treatments.
Check for specific catalog numbers listed in the recall notice: 10010483, 10010453, 10010454, 10013072, 10013361, 10013890, 10015012, 10015862, 10062818, 10821753, 11171447, 11426964, 11532269, 11613191, 10015861A, 22000-B007T, 2202-0007, 2204-0007, 2206-0007, 2260-0500, 22600-0007T, 22601-B007T, 22602-B007T, 22603-B007T, 24001-0007, 2403-0007, 24301-0007T, 2441-0007, 2450-0500, 24600-0007, 24601-B007T, 2465-0007, 2466-0007. All lots with expiration dates through July 31, 2026.
The recall notice does not specify a remedy for affected products. Contact BD directly for further instructions.
We’ve drafted a message you can send BD to request your refund or repair — edit it as you like.
Subject: Recall Z-0349-2024 — BD BD Hello, I own a BD that is covered by recall Z-0349-2024 from BD. 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.
