MIAClass 2
Needle, Spinal, Short Term
FDA adverse event reports and recall history for needle, spinal, short term (product code MIA), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 227
- Deaths
- 1
- Injuries
- 79
- Malfunctions
- 127
Reports per year
312
213
414
1215
2316
1517
1418
919
520
421
1922
1223
2324
1425
1526
Source: FDA adverse event reports by year received, 2012–2026. 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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