What are FDA adverse event reports for Tubing, Pressure And Accessories?

The FDA's MAUDE (Manufacturer and User Facility Device Experience) database collects reports of adverse events involving medical devices. For Tubing, Pressure And Accessories, there are 459 total reports including 14 death reports and 63 injury reports. These reports are submitted by manufacturers, healthcare facilities, and patients. A high number of reports does not necessarily mean a device is unsafe, widely used devices naturally generate more reports.

How should I interpret MAUDE data for Tubing, Pressure And Accessories?

MAUDE reports are raw adverse event submissions, not confirmed safety findings. A report that a device was involved in a death does not mean the device caused the death. Reports vary in quality and completeness. The FDA uses MAUDE data as one input among many in its safety surveillance, it does not draw conclusions from individual reports. Always consult your healthcare provider about device safety questions.

2026 data FDA MAUDE openFDA

Tubing, Pressure And Accessories

Name: Tubing, Pressure And Accessories - FDA MAUDE Adverse Event Reports
Creator: PlainHospital
License: https://creativecommons.org/publicdomain/zero/1.0/

Adverse-event figures are drawn from the U.S. Food & Drug Administration (FDA) MAUDE database, refreshed March 2026, see our methodology.

Compiled by PlainHospital · August 14, 2026

OpenFDA device adverse-event casebook.

Browse devices → Device safety hub

FDA MAUDE casebook

openFDA event book Tubing, Pressure And Accessories LIGHT-BOOK · MAUDE

#903 of 1000 · 459 reports · 1992–2026

BOOK 459 reports
RANK #903 of 1000
DEATH 14 death-typed
INJ 63 injury-typed
MALF 359 malfunction
SPAN 1992–2026
PEAK 2025: 68
PHOTO Test

Nearest event-volume peer: Test, Natriuretic Peptide (0 report gap)

Tubing, Pressure And Accessories sits #903 of 1000 among tracked device types with 459 MAUDE reports spanning 1992–2026. 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 →

Event-type mix vs corpus

Shares of FDA event_type codes on this device type, compared with the mean across 1,000 device types that have ≥100 MAUDE reports. Codes are report labels, not adjudicated causation.

DEATH 3.1% corpus 1.5% · above corpus mean (+1.5 pp)
INJ 13.7% corpus 30.4% · below corpus mean (-16.7 pp)
MALF 78.2% corpus 64.5% · above corpus mean (+13.7 pp)

Lead product-problem code Material Twisted/Bent is 16% of coded problems · Lead manufacturer TELEFLEX MEDICAL accounts for 45% of manufacturer-tagged reports · Top event location is 62% of location-tagged rows .

Connector

463
Insufflator

463
Tubing (this)

459
Test

459
Mask, Oxygen

456
Orthosis

455

What this shows Tubing, Pressure And Accessories carries 459 MAUDE reports, ranked #903 of 1000.

Event Types

Malfunction 359 (78.2%)

Injury 63 (13.7%)

Death 14 (3.1%)

12 (2.6%)

Other 11 (2.4%)

Patient Outcomes

FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.

335 (71.9%)

Other 80 (17.2%)

Required Intervention 18 (3.9%)

Death 13 (2.8%)

Life Threatening 7 (1.5%)

H 3 (0.6%)

O 3 (0.6%)

R 3 (0.6%)

Hospitalization 2 (0.4%)

S 1 (0.2%)

Invalid Data 1 (0.2%)

Yearly Trend

1992: 1

1993: 3

1995: 1

1996: 5

1997: 4

1998: 1

1999: 7

2000: 11

2001: 12

2002: 15

2003: 12

2004: 12

2005: 22

2006: 10

2007: 9

2008: 6

2009: 3

2010: 9

2011: 10

2012: 6

2013: 11

2014: 10

2015: 17

2016: 19

2017: 19

2018: 13

2019: 16

2020: 32

2021: 13

2022: 10

2023: 25

2024: 25

2025: 68

2026: 22

Top Manufacturers

TELEFLEX MEDICAL 45

MAQUET SAS 41

MERIT MEDICAL SYSTEMS, INC. 13

Event Locations

284 (61.9%)

I 99 (21.6%)

HOSPITAL 52 (11.3%)

NO INFORMATION 11 (2.4%)

INVALID DATA 5 (1.1%)

OTHER 3 (0.7%)

HOME 2 (0.4%)

AMBULATORY SURGICAL FACILITY 1 (0.2%)

OUTPATIENT TREATMENT FACILITY 1 (0.2%)

UNKNOWN 1 (0.2%)

Compare TELEFLEX MEDICAL vs MAQUET SAS →

Nationwide devices with similar MAUDE profiles

Two openFDA-derived peer sets for Tubing, Pressure And Accessories, both floored at ≥100 reports so the neighborhoods stay in the advertised mass.

Similar report volume

Nearest other device types by FDA MAUDE report count (459 here).

Test, Natriuretic Peptide 459 Mask, Oxygen 456 Connector, Airway 463 Insufflator 463

Similar death-typed counts

Nearest other device types by death-typed report count (14 here), distinct from the volume row.

Catheter And Tip, Suction 14 Display, Cathode-Ray Tube, Medical 14 Endoscopic Tissue Approximation Device 14 Glucose Oxidase, Glucose 14

Read our methodology - how this data is sourced, computed, and verified.

Disclaimer: MAUDE figures for Tubing, Pressure And Accessories 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 Tubing, Pressure And Accessories; 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.

Tubing, Pressure And Accessories

Event-type mix vs corpus