UNK
FDA adverse event reports naming UNK as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: UNK.
- Total reports
- 12,255
- Deaths
- 356
- Injuries
- 7,790
- Malfunctions
- 2,549
Reports per year
14712
15613
8014
11615
23016
45917
59318
61619
49320
72321
50322
63023
53624
46725
44826
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-FilledFTR2,414
- Prosthesis, Breast, Inflatable, Internal, SalineFWM1,569
- Excimer Laser SystemLZS439
- Mesh, Surgical, PolymericFTL287
- Screw, Fixation, BoneHWC214
- Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella EuaQKR192
- Latex Patient Examination GloveLYY151
- Port & Catheter, Implanted, Subcutaneous, IntravascularLJT150
- Set, Administration, IntravascularFPA137
- Needle, Hypodermic, Single LumenFMI124
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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