Reported Jun 19, 2024 · Ongoing
Stimuplex A, 30 DEG, 22GX2", 0.70x50mm, Catalogue Number: 4894502
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 DEG22GX2"0.70x50mm
- Catalogue Number4894502
- Lot codes and dates
- Catalogue Number4894502
- UDI/DI04022495101310
- Lot/Batch
207 of 207 codes
20E0120E0321E0721E0919E1022E1022E1121E1320E1920E2019E2119E2220E2223E2620E2723E3119F1219F1319F1519G0319G0419G0619G0919G2019G2119G2419G2519G2719H2319H2819H3019I1119I2119I2519I2619K1119K1619K1719K2419K2519L1219L1319L1519L1919M1219M1419M1719M2119M2419M2620A3020A3120B1520B1820B1920B2120B2620B2720C1420C17
- Amount recalled
- 1,157,640 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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