C.R. BARD, INC. (COVINGTON) -1018233
Manufacturer adverse-event records for C.R. BARD, INC. -1018233 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 · 2011–2026 · heavy-book · quiet Death-code · balanced
Volume signature
C.R. BARD, INC. -1018233 sits in the heavy MAUDE book
C.R. BARD, INC. (COVINGTON) -1018233 accounts for 47,321 FDA MAUDE reports (#78 of 443, heavy-book tercile). Death-coded event_type share is 0.06% (quiet); Injury share 16.0% (balanced).
What the volume reading shows for C.R. BARD, INC. (COVINGTON) -1018233
The standout signal for C.R. BARD, INC. (COVINGTON) -1018233 is filing volume: 47,321 adverse-event reports in FDA MAUDE (#78 of 443, heavy-book). Death-coded event_type share sits at 0.06% (quiet).
As a heavy-book manufacturer, portfolio size and reporting obligations inflate absolute counts - pair C.R. BARD, INC. -1018233 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 39,720 (83.9% of event_type total). Peak single-year volume reaches 7,026 reports across 16 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.