Midline Catheter
Adverse-event figures are drawn from the U.S. Food & Drug Administration (FDA) MAUDE database, refreshed March 2026, see our methodology.
OpenFDA device adverse-event casebook.
FDA Class II (moderate risk, special controls required), regulated under 21 CFR §880.5200 (General Hospital panel).
FDA MAUDE casebook
openFDA event book Midline Catheter LIGHT-BOOK · MAUDE
#668 of 1000 · 983 reports · 2016–2026
- BOOK 983 reports
- RANK #668 of 1000
- DEATH 2 death-typed
- INJ 174 injury-typed
- MALF 806 malfunction
- SPAN 2016–2026
- PEAK 2022: 178
- PHOTO Hepatitis A Test
Nearest event-volume peer: Hepatitis A Test (Antibody And Igm Antibody) (1 report gap)
Midline Catheter sits #668 of 1000 among tracked device types with 983 MAUDE reports spanning 2016–2026. Rank counts report volume, not confirmed device fault. Event_type Death / Injury / Malfunction are one code per report — not the same population as patient-outcome rows ( methodology). Read with this device → · Lead manufacturer → · Similar-volume device →
Malfunction reports run above the device-type norm
Midline Catheter carries 82.0% MALFUNCTION-coded reports, 17.2pp above the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.
- DEATH 0.2% corpus 1.5% · below corpus mean (-1.3 pp)
- INJ 17.7% corpus 30.3% · below corpus mean (-12.6 pp)
- MALF 82.0% corpus 64.8% · above corpus mean (+17.2 pp)
Lead product-problem code Fluid/Blood Leak is 26% of coded problems · Lead manufacturer C.R. BARD, INC. (BASD) -3006260740 accounts for 65% of manufacturer-tagged reports · Top event location is 71% of location-tagged rows .
Midline Catheter in the event-volume neighbourhood
FDA MAUDE report totals among this device type and nearest nationwide peers
- Pack
Pack, Hot Or Cold, Water Circulating
984 reports
- Midline Cathe… (this)
Midline Catheter
983 reports
- Hepatitis A T…
Hepatitis A Test (Antibody And Igm Antibody)
982 reports
- Single-Use Re…
Single-Use Reprocessed Ultrasonic Surgical Instruments
980 reports
- Container
Container, Sharps
979 reports
- Bronchoscope…
Bronchoscope Accessory
977 reports
What this shows Midline Catheter carries 983 MAUDE reports, ranked #668 of 1000.
Event Types
Patient Outcomes
FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.
Top Product Problems
Yearly Trend
Reports in 2025 (145) held close to the prior two-year average of 153.
Related Entities for Midline Catheter
Top Manufacturers
Event Locations
Compare C.R. BARD, INC. (BASD) -3006260740 vs BARD ACCESS SYSTEMS →
Nationwide devices with a comparable volume-and-death footprint
Two openFDA-derived peer sets for Midline Catheter: nearest by total report volume and nearest by death-typed count, each floored at ≥100 reports so the neighborhoods stay in the advertised mass.
Similar report volume
Nearest other device types by FDA MAUDE report count (983 here).
Similar death-typed counts
Nearest other device types by death-typed report count (2 here), distinct from the volume row.
Read our methodology - how this data is sourced, computed, and verified.
Disclaimer: MAUDE figures for Midline Catheter are informational only and are not clinical advice. Report codes do not prove device causation. Consult a qualified clinician before acting on this data.
Every figure on PlainHospital is rendered directly from federal source data, no number is typed in by an editor. Event-type mix on this page is computed from FDA MAUDE codes for Midline Catheter; corpus means use device types with ≥100 reports. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.