Reported Jun 19, 2024 · Ongoing
Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260
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 DEG21GX4"0.80x100mm
- Catalogue Number4894260
- Lot codes and dates
- Catalogue Number4894260
- UDI/DI04022495101211
- Lot/Batch
277 of 277 codes
22E0720E0820E0923E0923E1019E1123E1123E1319E1420E1419E1519E1623E1723E1823E2022E2121E2522E2522E2720E2919E3020E3019E3122E3119F0419F0519F0719F2119F2219F2619F2719F2819F2919G3019H0119H0219H0719H0819H3119I0419I0619I0719K0119K0219K0419K0819K0919K2719K3019L0619L0719M0519M0719M1020A0920A1120A1520A1720B0520B06
- Amount recalled
- 1,783,991 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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