Stimuplex® 4894260Recalls & reported problems
B. Braun Medical Inc. · Stimuplex® A, 30° bevel (4894260) · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- May 17, 2024Open, Classified
The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.
Z-2132-2024 · Root cause: Component design/selection · FDA record ↗
Other STIMULATOR, NERVE, BATTERY-POWERED devices
- Stimuplex® 4894251B. Braun Medical Inc. · STIMULATOR, NERVE, BATTERY-POWERED1 recall0 reports
- Stimuplex® 4894502B. Braun Medical Inc. · STIMULATOR, NERVE, BATTERY-POWERED1 recall0 reports
- Stimuplex® 4894278B. Braun Medical Inc. · STIMULATOR, NERVE, BATTERY-POWERED1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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