MNKClass 1
Endoscopic Bite Block
FDA adverse event reports and recall history for endoscopic bite block (product code MNK), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 162
- Deaths
- 0
- Injuries
- 25
- Malfunctions
- 133
Reports per year
102
112
314
215
516
517
918
1619
1320
1521
1122
423
2124
3925
1726
Source: FDA adverse event reports by year received, 2002–2026. 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.
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