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Stimuplex® 4894278Recalls & reported problems

B. Braun Medical Inc. · Stimuplex® A, 30° bevel (4894278) · Class 2

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

  1. 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-2133-2024 · Root cause: Component design/selection · FDA record ↗

Other STIMULATOR, NERVE, BATTERY-POWERED devices

All STIMULATOR, NERVE, BATTERY-POWERED devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.