Catheter, Percutaneous, Long Term, Intraspinal
FDA adverse event reports and recall history for catheter, percutaneous, long term, intraspinal (product code LNY), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 158
- Deaths
- 1
- Injuries
- 115
- Malfunctions
- 26
Reports per year
Source: FDA adverse event reports by year received, 2003–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
- 2004-07-20TerminatedOther
Port-A-Cath II Low Profile Epidural Implantable Access System, with PolyFlow Polyurethane Catheter, 1.2mm O.D. x 0.5mm I.D., REF 21-1501-01
Some of the outer product pouches have voids in the seals and do not assure that the outer surfaces of the inner tray containing the port, catheter and procedural components remain sterile after sterilization.
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