MDT PUERTO RICO OPERATIONS CO
Manufacturer adverse-event records for MDT PUERTO RICO OPERATIONS CO come from the U.S. Food & Drug Administration (FDA) MAUDE database via openFDA, refreshed March 2026 - see our methodology. Not medical advice.
FDA MAUDE device safety record · 2007–2026 · heavy-book · typical Death-code · injury-heavy
Volume signature
MDT PUERTO RICO OPERATIONS CO sits in the heavy MAUDE book
MDT PUERTO RICO OPERATIONS CO accounts for 35,495 FDA MAUDE reports (#97 of 443, heavy-book tercile). Death-coded event_type share is 0.66% (typical); Injury share 67.6% (injury-heavy).
What the volume reading shows for MDT PUERTO RICO OPERATIONS CO
The standout signal for MDT PUERTO RICO OPERATIONS CO is filing volume: 35,495 adverse-event reports in FDA MAUDE (#97 of 443, heavy-book). Death-coded event_type share sits at 0.66% (typical).
As a heavy-book manufacturer, portfolio size and reporting obligations inflate absolute counts - pair MDT PUERTO RICO OPERATIONS CO with device-family pages before treating company totals as a safety verdict. Event_type Death and Injury are one code per report; Patient Outcomes below use a separate FDA population.
Reports span 17 device types, led in this extract by Injury at 24,008 (67.6% of event_type total). Peak single-year volume reaches 6,264 reports across 20 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.
Event Types
Patient Outcomes
FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.
Devices (17)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.