Mcghan Medical Corp.
FDA adverse event reports naming Mcghan Medical Corp. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MCGHAN MEDICAL CORP..
- Total reports
- 1,219
- Deaths
- 13
- Injuries
- 915
- Malfunctions
- 116
Reports per year
2493
22094
10695
12396
17297
26098
16499
11200
1401
602
1103
204
106
109
211
Source: FDA adverse event reports by year received, 1993–2011. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-FilledFTR593
- Prosthesis, Breast, Inflatable, Internal, SalineFWM454
- Implant, Dermal, For Aesthetic UseLMH96
- Tissue Expander And AccessoriesLCJ64
- Prosthesis, Chin, InternalFWP4
- Product code 3
- Prosthesis, Nose, InternalFZE2
- Joint, Temporomandibular, ImplantLZD2
- Implant, MalarLZK2
- Prosthesis, TesticularFAF1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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