B Braun recalls Stimuplex A needles with DEHP traces in glue. These medical needles may cause health issues if used. Affected units have specific catalog numbers and batch dates.
The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.
B Braun is recalling certain Stimuplex A needles because the glue used contains traces of DEHP, a chemical linked to health risks. This recall affects medical needles used in procedures requiring precise insertion. Using these needles could pose health risks if the DEHP traces are absorbed through skin contact.
The glue in these needles contains traces of DEHP, a chemical that can cause health issues if absorbed through skin contact during medical procedures. DEHP is a known endocrine disruptor and can lead to health problems with prolonged exposure.
Medical professionals using these needles for procedures are most at risk. Patients receiving these needles during medical treatments could also be affected.
Check for the catalog number 4894251 on the needle packaging. Affected units were produced in batches labeled 20E15, 19L09, 19L27, 20A19, 20H21, 21G14, 21I16, 22H23.
Look for the catalog number 4894251 on the needle packaging to confirm if it is affected.
DEHP is a chemical that can cause health issues if absorbed through skin contact during medical procedures. It is a known endocrine disruptor and can lead to health problems with prolonged exposure.
The recall record does not specify a remedy, so no action is required beyond checking if you have the affected needles.
Yes, affected units were produced in batches labeled 20E15, 19L09, 19L27, 20A19, 20H21, 21G14, 21I16, 22H23.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2131-2024 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-2131-2024 from B Braun. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
