Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled "not made with DEHP"...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact B Braun Medical Inc directly.
Affected Products
Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260
Quantity: 1,783,991 units
Why Was This Recalled?
The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About B Braun Medical Inc
B Braun Medical Inc has 148 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report