MDT Puerto Rico Operations Co., Juncos
FDA adverse event reports naming MDT Puerto Rico Operations Co., Juncos as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MDT PUERTO RICO OPERATIONS CO., JUNCOS.
- Total reports
- 10,885
- Deaths
- 105
- Injuries
- 5,553
- Malfunctions
- 5,210
Reports per year
4007
30909
6,00010
4,53311
312
Source: FDA adverse event reports by year received, 2007–2012. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW4,356
- Pump, Infusion, Implanted, ProgrammableLKK3,161
- Stimulator, Electrical, Implantable, For IncontinenceEZW1,824
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY1,345
- Intestinal StimulatorLNQ195
- Blade, ScalpelGES1
- Unit, Electrosurgical, Endoscopic (With Or Without Accessories)KNS1
- Lithotriptor, Extracorporeal Shock-Wave, UrologicalLNS1
- Sensor, Glucose, InvasiveMDS1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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