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 corpus and the live FDA recall database.
- Total reports
- 438
- Deaths
- 0
- Injuries
- 242
- Malfunctions
- 196
Reports per year
421
2722
5823
10324
14925
9726
Source: FDA adverse event reports by year received, 2021–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor stimulator, neuromuscular, lower back muscles, totally implanted for pain relief automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.