B Braun recalls Stimuplex A 30-degree 22G needles with DEHP traces in glue. These medical needles may cause health issues if used repeatedly. Check your product's catalog number for affected lots.
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 medical needles because the glue used contains traces of DEHP, a chemical that can be harmful with repeated use. This recall affects specific lots and catalog numbers.
The glue in these needles contains small amounts of DEHP, a plasticizer that can leach into the body over time. While the devices are labeled 'DEHP free,' the glue has traces of this chemical, which may cause health issues with repeated use.
Medical professionals and patients using the recalled Stimuplex A needles. Those with frequent needle use are at slightly higher risk due to potential chemical exposure.
Check for the product name 'Stimuplex A', 30 DEG, 22GX2", 0.70x50mm, and catalog number 4894502. Affected lots include specific batch numbers listed in the recall notice.
Identify the catalog number and lot/batch numbers listed in the recall notice to confirm if your needle is affected.
The glue contains traces of DEHP, a chemical that can leach into the body over time with repeated use, potentially causing health issues.
Check for the product name 'Stimuplex A', 30 DEG, 22GX2", 0.70x50mm, and catalog number 4894502. Affected lots include specific batch numbers listed in the recall notice.
The recall does not require immediate discontinuation; however, you should check if your needle is affected and avoid using it if it matches the listed lots.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2134-2024 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-2134-2024 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.
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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.
