Medical Engineering Corp.
FDA adverse event reports naming Medical Engineering Corp. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDICAL ENGINEERING CORP..
- Total reports
- 1,636
- Deaths
- 14
- Injuries
- 1,290
- Malfunctions
- 108
Reports per year
1993
31194
12495
12396
78497
21998
3999
1200
101
203
208
Source: FDA adverse event reports by year received, 1993–2008. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-FilledFTR1,168
- Device, Impotence, Mechanical/HydraulicFHW431
- Prosthesis, Breast, Inflatable, Internal, SalineFWM12
- Tissue Expander And AccessoriesLCJ10
- Prosthesis, PenileFAE5
- Prosthesis, Chin, InternalFWP3
- Tubes, Gastrointestinal (And Accessories)KNT3
- Stent, UreteralFAD2
- Prosthesis, TesticularFAF2
- Product code FTBFTB1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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