MLQClass 3
Inhibitor, Peridural Fibrosis (Adhesion Barrier)
FDA adverse event reports and recall history for inhibitor, peridural fibrosis (adhesion barrier) (product code MLQ), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 440
- Deaths
- 2
- Injuries
- 420
- Malfunctions
- 5
Reports per year
499
8300
32401
2202
603
108
Source: FDA adverse event reports by year received, 1999–2008. 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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