TELEFLEX MEDICAL
Manufacturer adverse-event records for TELEFLEX MEDICAL 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 · 2004–2026 · heavy-book · typical Death-code · injury-light
Injury-mix signature
TELEFLEX MEDICAL is lighter on Injury codes
Injury-coded event_type share is 2.4% (injury-light tercile) beside 0.36% Death-coded (typical). Volume band: heavy.
What the Injury-mix reading shows for TELEFLEX MEDICAL
The standout signal for TELEFLEX MEDICAL is Injury-mix: 2.4% Injury-coded (injury-light) beside 0.36% Death-coded, on a heavy-book footprint.
As a heavy-book manufacturer, portfolio size and reporting obligations inflate absolute counts - pair TELEFLEX MEDICAL 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 20 device types, led in this extract by Malfunction at 28,182 (96.8% of event_type total). Peak single-year volume reaches 2,797 reports across 23 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 (20)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.