DZM
Product code DZM
FDA adverse event reports and recall history for product code dzm (product code DZM), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 680
- Deaths
- 0
- Injuries
- 358
- Malfunctions
- 292
Reports per year
1712
1813
1014
1015
3716
2517
3818
3119
1620
4121
3522
3423
2724
1125
926
Source: FDA adverse event reports by year received, 2012–2026. 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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