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Abbott Implantable Neurostimulator AU
No active recall
Manufacturer: Abbott · FDA product code: PMP · Category: Dorsal Root Ganglion Stimulator For Pain Relief
Severity Snapshot
43 total reports2016-06 – 2024-02 date range9.3% physician / facility reported90.7% manufacturer reported1 SKU variants
Failure & Consequence Profiles
Top Failure Modes
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Top Patient Outcomes
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Reporting Trend
Annual Reporting Volume
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Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.
Reported Events
Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.
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