AMO PUERTO RICO MFG. INC.
Manufacturer adverse-event records for AMO PUERTO RICO MFG. INC. 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 · 2020–2026 · mid-book · quiet Death-code · balanced
Death-code intensity
AMO PUERTO RICO MFG. INC. is quieter on Death-coded events
Death-coded event_type rows are 0 of 11,598 (0.00% · quiet tercile among 434 manufacturers). Absolute volume is mid-book.
What the Death-code reading shows for AMO PUERTO RICO MFG. INC.
The standout signal for AMO PUERTO RICO MFG. INC. is Death-code intensity: 0.00% of 11,598 reports (quiet tercile), while absolute volume is mid-book.
Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for AMO PUERTO RICO MFG. INC.. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.
Reports span 9 device types, led in this extract by Malfunction at 7,675 (66.2% of event_type total). Peak single-year volume reaches 2,230 reports across 7 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 (9)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.