LKGClass 2
Port & Catheter, Implanted, Subcutaneous, Intraventricular
FDA adverse event reports and recall history for port & catheter, implanted, subcutaneous, intraventricular (product code LKG), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 109
- Deaths
- 1
- Injuries
- 40
- Malfunctions
- 66
Reports per year
109
211
113
114
315
116
718
419
320
821
622
1023
324
1425
426
Source: FDA adverse event reports by year received, 2009–2026. 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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