QLKClass 3
Stimulator, Neuromuscular, Lower Back Muscles, Totally Implanted For Pain Relief
FDA adverse event reports and recall history for stimulator, neuromuscular, lower back muscles, totally implanted for pain relief (product code QLK), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 420
- Deaths
- 0
- Injuries
- 229
- Malfunctions
- 191
Reports per year
421
2722
5823
10324
14925
7926
Source: FDA adverse event reports by year received, 2021–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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