Enteral Specific Transition Connectors
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 §876.5980 (Gastroenterology, Urology panel).
FDA MAUDE casebook
openFDA event book Enteral Specific Transition Connectors LIGHT-BOOK · MAUDE
#968 of 1000 · 402 reports · 2015–2026
- BOOK 402 reports
- RANK #968 of 1000
- DEATH 2 death-typed
- INJ 6 injury-typed
- MALF 390 malfunction
- SPAN 2015–2026
- PEAK 2016: 215
- PHOTO Device
Nearest event-volume peer: Device, Medical Examination, Ac Powered (1 report gap)
Enteral Specific Transition Connectors sits #968 of 1000 among tracked device types with 402 MAUDE reports spanning 2015–2026. 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
Enteral Specific Transition Connectors carries 97.0% MALFUNCTION-coded reports, 32.2pp above the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.
- DEATH 0.5% corpus 1.5% · below corpus mean (-1.0 pp)
- INJ 1.5% corpus 30.3% · below corpus mean (-28.8 pp)
- MALF 97.0% corpus 64.8% · above corpus mean (+32.2 pp)
Lead product-problem code Leak/Splash is 75% of coded problems · Lead manufacturer MOOG MEDICAL DEVICES GROUP accounts for 94% of manufacturer-tagged reports · Top event location I is 88% of location-tagged rows .
Enteral Specific Transition Connectors in the event-volume neighbourhood
FDA MAUDE report totals among this device type and nearest nationwide peers
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Enteral Specific Transition Connectors
402 reports
- Device
Device, Medical Examination, Ac Powered
401 reports
What this shows Enteral Specific Transition Connectors carries 402 MAUDE reports, ranked #968 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 (10) held close to the prior two-year average of 8.
Related Entities for Enteral Specific Transition Connectors
Top Manufacturers
Event Locations
Nationwide devices with a comparable volume-and-death footprint
Two openFDA-derived peer sets for Enteral Specific Transition Connectors: 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 (402 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 Enteral Specific Transition Connectors 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 Enteral Specific Transition Connectors; 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.