Reported Jun 19, 2024 · Ongoing
Stimuplex A, 30 DEG, 20GX6", 0.90x150mm, Catalogue Number: 4894278
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 DEG20GX6"0.90x150mm
- Catalogue Number4894278
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published 4894278— — 04022495101266UDI/DI: 04022495101266 — Lot/Batch: 20E15, 21E18, 19F08, 19G10, 19G13, 19G19, 19I19, 20C28, 20C31, 20D10, 20L19, 21B13, 21I17, 21K21, 21L12, 21M16, 22D12, 22H20, 22I22, 22K27, 23A20, 23C04, 23D14, 23F09, 23I08, 23I29 - Amount recalled
- 108,811 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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