Reported Jun 19, 2024 · Ongoing
Stimuplex A, 30 DEG, 24GX1", 0.55x25mm, Catalogue Number: 4894251.
B Braun Medical Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: B Braun Medical Inc · 200 Boulder Dr · Breinigsville, PA · 18031-1532
Is this the product you have?
Stimuplex A30 DEG24GX1"0.55x25mm
- Catalogue Number4894251
- Lot codes and dates
- Catalogue Number4894251
- UDI/DI04022495101167
- Lot/Batch
20E1519L0919L2720A1920H2121G1421I1622H23
- Amount recalled
- 20,850 units
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
Why it was recalled
The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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