Triever20Recalls & reported problems across all models
Inari Medical, Inc. · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 20
- Deaths reported
- 8
- Injuries reported
- 9
- Recalls
- 0
We found 2 models of Triever20 by Inari Medical, Inc. in the FDA's device registry (GUDID). Together they are named in 20 adverse event reports in the FDA's MAUDE database, received between Aug 19, 2017 and Jul 1, 2025 — classified as 8 deaths, 9 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (6 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Triever20 problems
Device problems
- Improper or Incorrect Procedure or Method6
- Adverse Event Without Identified Device or Use Problem5
- Material Separation3
- Difficult to Remove2
- Entrapment of Device2
- Insufficient Device Problem Information2
- Retraction Problem2
- Use of Device Problem2
Patient problems
- Low Blood Pressure/ Hypotension5
- Cardiac Arrest4
- Hemoptysis4
- Perforation of Vessels4
- Death3
- Loss of consciousness3
- Low Oxygen Saturation3
- Pericardial Effusion3
Triever20 models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Triever20 21-101Peripheral Mechanical Thrombectomy With Aspiration8 deaths18 reports
- Triever20 21-101Peripheral Mechanical Thrombectomy With Aspiration2 reports
Recent Triever20 adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJul 1, 2025Retraction Problem; Material Separation; Retraction Problem; Material Separation
ON (B)(6) 2025, A PATIENT UNDERWENT DEEP VEIN THROMBOSIS (DVT) THROMBECTOMY USING INARI DEVICES. THE PATIENT'S CLOT AGE WAS ESTIMATED AT 14 DAYS. WHEN ATTEMPTING TO REMOVE THE TRIEVER 20 AFTER THE FINAL ASPIRATION, THE CATHETER BECAME STUCK IN THE PATIENT'S VESSEL. FOLLOWING MULTIPLE ATTEMPTS TO REMOVE THE DEVICE USING BALLOONING AND MEDICATION, THE DEVICE SEPARATED AND APPROXIMATELY 10-15CM OF THE CATHETER REMAINED IN THE PATIENT. THE MEDICAL TEAM WAS UNSUCCESSFUL IN REMOVING THE REMAINING PART OF THE CATHETER DURING THE PROCEDURE, HOWEVER; THE MEDICAL TEAM WAS ABLE TO REMOVE THE PIECE OF THE DEVICE THE FOLLOWING DAY.
Patient problems: Foreign Body In Patient
MAUDE report 22375105 ↗MalfunctionMar 4, 2025Entrapment of Device; Difficult to Remove; Material Separation; Entrapment of Device; Difficult to Remove; Material Separation
ON (B)(6) 2025, A 49-YEAR-OLD MALE UNDERWENT DEEP VEIN THROMBOSIS (DVT) THROMBECTOMY USING INARI DEVICES. THE PATIENT'S CLOT AGE WAS ESTIMATED AT 90 DAYS. DURING THE THROMBECTOMY, THE TREIVER20 CATHETER (T20) WAS ADVANCED WITHOUT AN INTRODUCER SHEATH INTO THE LEFT POPLITEAL VEIN. AN ASPIRATION WAS PERFORMED, AND THE CATHETER WAS RETRACTED. THE TIP OF THE CATHETER BECAME STUCK WHILE RETRACTING THE CATHETER THROUGH THE COMMON ILIAC VEIN. THE CATHETER WAS RETRACTED A FEW MORE INCHES AND THEN FRACTURED. HALF OF THE CATHETER AND THE DILATOR WERE REMOVED AND APPROXIMATELY 20 CENTIMETERS OF THE T20 DELIVERY CATHETER REMAINED IN THE PATIENT'S VESSEL. SCISSORS WERE USED TO CUT THE WIRE BRAIDING OF THE T20. AN INTRI24 INTRODUCER SHEATH (INTRI24) WAS THEN ADVANCED TO WHERE THE TIP WAS JUST OVER THE PROXIMAL (BROKEN) END OF THE T20 AND A 10X40 BALLOON WAS PLACED OVER THE WIRE AT THE DISTAL END OF THE REMAINING PORTION OF THE T20 CATHETER INTO THE INTRI24. THE INTRI24, T20 CATHETER, AND BALLOON WERE THEN REMOVED TOGETHER AND THE INTRI24 WAS FLUSHED AND REPLACED INTO THE LEFT POPLITEAL VEIN. ALL MATERIAL WAS CONFIRMED TO BE REMOVED FROM THE PATIENT AND THE PATIENT SUSTAINED NO INJURIES. THE PATI
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21520940 ↗MalfunctionFeb 13, 2025Entrapment of Device; Difficult to Remove; Material Separation; Difficult to Advance; Entrapment of Device; Difficult to Remove; Material Separation; Difficult to Advance
ON (B)(6) 2025, A 47-YEAR-OLD FEMALE UNDERWENT A DEEP VEIN THROMBOSIS (DVT) THROMBECTOMY USING INARI DEVICES. THE PATIENT HAD A PREEXISTING INFERIOR VENA CAVA (IVC) FILTER. THE PATIENT'S CLOT AGE WAS ESTIMATED AT 100 DAYS. DURING THE THROMBECTOMY, THE TREIVER20 CATHETER (T20) WAS ADVANCED WITHOUT AN INTRODUCER SHEATH INTO THE RIGHT POPLITEAL VEIN TO TARGET CLOT IN THE RIGHT FEMORAL VEIN. WHILE TRYING TO MOVE THE CATHETER WITHIN THE VESSEL, THE CATHETER BECAME STUCK AND WOULD NOT ADVANCE OR RETRACT. THE CATHETER THEN SEPARATED, LEAVING THE TWO HALVES CONNECTED BY THE INNER COIL. AN ATTEMPT WAS MADE TO REMOVE THE CATHETER USING A MUSTANG BALLOON; HOWEVER, THE ATTEMPT WAS UNSUCCESSFUL. AFTER TWO DOSES OF NITROGLYCERIN WERE ADMINISTERED, THE PHYSICIAN WAS ABLE TO REMOVE THE CATHETER IN FULL BY TWISTING IT CLOCKWISE. THERE WERE NO INJURIES TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21380045 ↗InjuryDec 5, 2024Use of Device Problem; Use of Device Problem
AN 82-YEAR-OLD FEMALE PRESENTED TO THE EMERGENCY DEPARTMENT DUE TO ONGOING SHORTNESS OF BREATH. THE PATIENT HAD BEEN EXPERIENCING SYMPTOMS FOR MORE THAN 5 DAYS. IMAGING REVEALED LARGE CLOT BURDEN IN THE RIGHT ATRIUM (RA) WHICH WAS A CLOT-IN-TRANSIT (CIT). ADDITIONALLY, THE PATIENT HAD A SADDLE PULMONARY EMBOLISM (PE) IN THE MAIN PULMONARY ARTERY (MPA) AND BILATERAL PE IN THE RIGHT PULMONARY ARTERY (RPA) AND LEFT PULMONARY ARTERY (LPA). REMOVAL OF THE CIT WAS SUCCESSFUL. THE 1ST ASPIRATION YIELDED SUBSTANTIAL THROMBUS. THE PHYSICIAN INSERTED THE DILATOR AND ADVANCED THE TRIEVER24 (T24) TO ENGAGE WITH THE CLOT AND DID 2 ADDITIONAL PULLS, COMPLETELY REMOVING CLOT FROM THE RA. THE PHYSICIAN PROCEEDED TO CROSS THE RIGHT HEART AND TAKE PRESSURE MEASUREMENTS. DUE TO THE PATIENT'S PRESSURES, THERE WAS DISCUSSION ON ENDING THE CASE, BUT THE PHYSICIAN WANTED TO QUICKLY ADDRESS THE PULMONARY ARTERIES. WIRE POSITION WAS OBTAINED AND THE T24 WAS ADVANCED. THE T24 CAUSED THE WIRE TO PUSH OUT AND DUE TO THE HIGH PRESSURES, THE PHYSICIAN SWITCHED TO A TRIEVER20 (T20). THE T20 WAS ADVANCED INTO THE MPA, AND MULTIPLE ASPIRATIONS YIELDED ORGANIZED CLOT. THE PHYSICIAN THEN ADVANCED THE T20 WITHOUT THE
Patient problems: Cardiogenic Shock; Extravasation; Hemorrhage/Blood Loss/Bleeding; Perforation of Vessels
MAUDE report 20858091 ↗InjuryApr 23, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A 71-YEAR-OLD FEMALE PATIENT WITH ESOPHAGEAL CANCER WAS DIAGNOSED WITH BILATERAL PULMONARY EMBOLISM (PE) VIA COMPUTED TOMOGRAPHY ANGIOGRAPHY. THE PATIENT WAS SCHEDULED FOR THROMBECTOMY USING INARI DEVICES. THE CLOT AGE WAS ESTIMATED AT 7 DAYS. WIRE POSITIONING WAS OBTAINED WITHOUT ISSUE AND A TRIEVER20 (T20) CATHETER WAS ADVANCED INTO PLACE. AN ASPIRATION WAS PERFORMED IN THE RIGHT PULMONARY ARTERY WHICH DID NOT YIELD CLOT. THE T20 WAS ADVANCED AGAIN, AND A SECOND ASPIRATION WAS PERFORMED; HOWEVER, THE CLOT BECAME LODGED IN THE TIP OF THE T20. THE PHYSICIAN PROCEEDED TO REMOVE THE T20 CATHETER FROM THE PATIENT THROUGH THE INARI INTRI24 SHEATH. UPON INITIAL EXAMINATION, THERE WAS NO CLOT PRESENT IN THE LARGE BORE SYRINGE OR CATHETER. THE INTRI24 SHEATH WAS REMOVED UNDER PRESSURE AND FLUSHED, WHICH YIELDED A LARGE PORTION OF CLOT. THERE WAS ALSO A LARGE CLOT PRESENT AT THE ACCESS SITE WHICH WAS REMOVED MANUALLY. THE INTRI24 SHEATH AND T20 CATHETER WERE CLEANED AND ADVANCED BACK INTO PLACE WHEN THE PATIENT REPORTED EXPERIENCING DIPLOPIA IN THE LEFT EYE AND VERTIGO AND SHOWED SIGNS OF RESTLESSNESS. A RAPID RESPONSE WAS INITIATED; THE PATIENT RESPONDED TO VERBAL COMMANDS, BUT WAS UNABLE
Patient problems: Anxiety; Stroke/CVA; Vertigo; Visual Disturbances
MAUDE report 19169748 ↗InjuryFeb 1, 2024Material Fragmentation; Material Fragmentation
A FEMALE PATIENT WITH LEFT LOWER EXTREMITY DEEP VEIN THROMBOSIS (DVT) UNDERWENT A THROMBECTOMY ON (B)(6), 2024 USING THE INARI TRIEVER20 (T20). THE CLOT AGE WAS ESTIMATED AT 14 DAYS. THREE ACCESS POINTS WERE MADE IN THE RIGHT INTRAJUGULAR, LEFT POPLITEAL, AND RIGHT POPLITEAL. WIRE POSITIONING WAS OBTAINED WITHOUT ISSUE AND THE TRIEVER20 WAS ADVANCED WITHOUT AN INTRODUCER SHEATH. SEVERAL ASPIRATIONS WERE PERFORMED WHICH CLEARED THE ENTIRE CLOT FROM THE LEFT POPLITEAL VEIN. AS THE T20 CATHETER WAS BEING REMOVED, A PORTION DETACHED AND THE PHYSICIAN HALTED THE PROCEDURE TO PERFORM IMAGING. A VASCULAR SURGEON INTERVENED TO PERFORM A VENOUS CUT-DOWN TO REMOVE THE REMAINING PORTION OF THE CATHETER. ALL DEVICE FRAGMENTS WERE REMOVED SUCCESSFULLY; THE CUT-DOWN AND POPLITEAL VEINS WERE CLOSED AND A FINAL VENOGRAM WAS PERFORMED. ON (B)(6), 2024 FOLLOW-UP WAS REQUESTED FROM THE TREATING PHYSICIAN WHO REPORTED THE PATIENT WAS "DOING GREAT" POSTOPERATIVELY.
Patient problems: Device Embedded In Tissue or Plaque; Vascular Dissection
MAUDE report 18628534 ↗InjuryMar 17, 2023Retraction Problem; Activation, Positioning or Separation Problem; Retraction Problem; Activation, Positioning or Separation Problem
A 56-YEAR-OLD FEMALE WITH DEEP VEIN THROMBOSIS (DVT) UNDERWENT A THROMBECTOMY IN THE LEFT LEG WITH THE INARI FLOWTRIEVER SYSTEM ON (B)(6) 2023. THE PATIENT ALSO HAD AN INFERIOR VENA CAVA (IVC) FILTER PLACED 90 DAYS PRIOR. THE TRIEVER20 (T20) WAS DEPLOYED AND 5 ASPIRATIONS WERE PERFORMED IN THE LEFT LEG WITH APPROXIMATELY 225 CC OF BLOOD RETURNED VIA THE INARI FLOWSAVER DEVICE TO THE RIGHT LEG (POPLITEAL ACCESS). A PENUMBRA INDIGO SYSTEM CAT 8 DEVICE WAS THEN USED TO CLEAR COLLATERAL THROMBUS. THE T20 WAS RE-INSERTED TO CLEAR THROMBUS FROM THE FEMORAL-POPLITEAL, COMMON FEMORAL, AND EXTERNAL ILIAC VEINS. HOWEVER, THE T20 BECAME CAUGHT IN THE VESSEL. THE SURGEON MADE VARIOUS ATTEMPTS TO REMOVE THE T20, INCLUDING USE OF VASODILATORS, LUBRICANTS, AND BALLOONING, BUT THE T20 WAS UNABLE TO BE REMOVED. BEFORE THE SECOND BALLOONING ATTEMPT, THE T20 SHEARED AT THE POPLITEAL ACCESS. EVENTUALLY, CARDIOTHORACIC SURGERY INTERVENED TO PERFORM A VENOUS CUTDOWN ON THE COMMON FEMORAL VEIN AND THE T20 WAS REMOVED. THE THROMBECTOMY WAS SUCCESSFUL IN REMOVING 90% OF THE CLOT BURDEN AND THE PATIENT MADE A FULL RECOVERY.
Patient problems: Device Embedded In Tissue or Plaque; Perforation of Vessels
MAUDE report 16568390 ↗DeathApr 14, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A (B)(6) YEAR-OLD MALE PATIENT WITH A RARE BLOOD CLOTTING DISORDER PRESENTED TO THE EMERGENCY DEPARTMENT IN UNSTABLE CONDITION WITH CLOTTING ABOVE HIS EXISTING INFERIOR VENA CAVA (IVC) FILTER. THE PATIENT ALSO HAD BILATERAL DEEP VEIN THROMBOSIS (DVT) IN BOTH LEGS. THE IVC FILTER WAS PLACED 9 DAYS PRIOR AND THE PATIENT UNDERWENT SPINAL SURGERY 5 DAYS PRIOR. THE COMPUTERIZED TOMOGRAPHY (CT) SCAN DID NOT SHOW A PULMONARY EMBOLISM. ANTICOAGULANT MEDICATION HAD BEEN DISCONTINUED SINCE THE TIME OF IVC FILTER PLACEMENT AND WAS NOT REINITIATED. THE TREATMENT PLAN WAS TO USE THE INARI FLOWTRIEVER 20 (T20) TO ADDRESS CLOTTING ABOVE AND IN THE IVC FILTER AND THEN USE THE INARI CLOTTRIEVER TO ADDRESS THE DVTS IN THE LEGS. AN ECHOCARDIOGRAM WAS NOT PERFORMED PRIOR TO THE PROCEDURE. AN ACTIVATED CLOTTING TIME (ACT) TEST WAS RUN AND THE ADVISING NEUROSURGEON REQUESTED LIMITING ANTICOAGULANTS. THE PATIENT WAS INTUBATED AND PLACED ON VASOPRESSORS. A 22 FR GORE DRYSEAL SHEATH WAS PLACED IN THE NECK AND AN 8 FR SHEATH WAS PLACED IN THE LEFT POPLITEAL VEIN. TWO INTERVENTIONAL RADIOLOGISTS WERE PRESENT, THE PRIMARY PHYSICIAN WAS ASSIGNED TO TREAT THE IVC CLOT WITH THE T20 AND THE SECOND PHYSICIAN PROVI
Patient problems: Bradycardia; Cardiac Arrest; Cardiogenic Shock; High Blood Pressure/ Hypertension; Low Oxygen Saturation
MAUDE report 14115743 ↗DeathNov 24, 2021Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method
A (B)(6) FEMALE PRESENTED TO THE EMERGENCY DEPARTMENT ON (B)(6) 2021 WITH A BILATERAL PULMONARY EMBOLISM. THE PATIENT HAD A HISTORY OF A 3-VESSEL CORONARY ARTERY BYPASS GRAFT (CABG) SURGERY, ABDOMINAL AORTIC ANEURYSM (AAA) REPAIR, AND HYPERTENSION. THE PATIENT WAS ON A FLIGHT APPROXIMATELY 2.5 WEEKS PRIOR TO PRESENTING TO THE HOSPITAL; IMMEDIATELY AFTER THE INITIAL FLIGHT SHE EXPERIENCED RIGHT ANKLE EDEMA AND TENDERNESS, FOLLOWED BY SHORTNESS OF BREATH AND CHEST PAIN. THE PATIENT FLEW HOME APPROXIMATELY 7 DAYS PRIOR TO PRESENTING TO THE HOSPITAL AND SYMPTOMS HAD WORSENED. ON (B)(6) 2021 THE PATIENT UNDERWENT AN ATTEMPTED THROMBECTOMY WITH THE INARI TRIEVER20 (T20). THE SURGICAL PLAN WAS TO TREAT THE RIGHT PULMONARY ARTERY FIRST. INTERNAL JUGULAR ACCESS WAS OBTAINED VIA ULTRASOUND GUIDANCE WITH A MICRO PUNCTURE SHEATH; THE SHEATH WAS EXCHANGED WITH A STANDARD 6 FR SHEATH. THE PHYSICIAN CROSSED THE RIGHT HEART WITH A COBRA CATHETER AND A BENTSON WIRE GUIDE. WHEN CROSSING THE HEART, THE PHYSICIAN REPORTED THE COBRA CATHETER TOOK A SLIGHTLY DIFFERENT PATH THAN EXPECTED. GOOD DISTAL WIRE POSITION WAS ACHIEVED IN THE RIGHT LOWER PULMONARY ARTERY, BUT THE WIRE CONTINUED TO CREEP BACK DURI
Patient problems: Cardiac Arrest; Cardiac Perforation; Hemoptysis; Intraoperative Pain; Loss of consciousness; Low Blood Pressure/ Hypotension; Low Oxygen Saturation; Perforation of Vessels; Pericardial Effusion; Pleural Effusion; Respiratory Arrest
MAUDE report 12870662 ↗DeathApr 17, 2021Insufficient Device Problem Information; Insufficient Device Problem Information
AN (B)(6) YEAR-OLD MALE PATIENT WITH DIABETES AND RECENT PNEUMONIA PRESENTED TO THE EMERGENCY DEPARTMENT ON (B)(6) 2021 EXPERIENCING SHORTNESS OF BREATH FOR THE PAST 2-3 DAYS. THE PATIENT HAD SEVERE SEPSIS, HYPOXIA, HYPERTENSION, AND ELEVATED TROPONINS, AND HIS FAMILY STATED THAT THE PATIENT WAS "NOT LUCID" UPON ADMISSION. A CT SCAN REVEALED BILATERAL PULMONARY EMBOLISM (PE) THAT WAS CLASSIFIED AS HIGH-RISK SUBMASSIVE, WITH A RV/LV RATIO OF 1.2 AND CONCOMITANT DEEP VEIN THROMBOSIS (DVT) THAT DID NOT WARRANT INTERVENTION. ON (B)(6) 2021, THE INARI TRIEVER16 (T16) AND TRIEVER24 (T24) WERE USED TO ATTEMPT TO TREAT THE PE. THE PATIENT WAS PLACED ON A HEPARIN DRIP AT THE BEGINNING OF THE PROCEDURE. HIS HEART RATE WAS 84 BPM, BLOOD PRESSURE 113/66 MMHG, SPO2 98%, AND HEMOGLOBIN 13. HIS BASELINE ACT WAS 126, AND 5,000 UNITS OF HEPARIN WERE ADMINISTERED. AFTER ACCESS WAS GAINED, A SWAN-GANZ CATHETER WAS USED TO TAKE A PULMONARY ARTERY (PA) PRESSURE MEASUREMENT OF 66/26/40, INDICATING THE PATIENT HAD SEVERE PULMONARY HYPERTENSION. IMAGING CONFIRMED THE PRESENCE OF CLOT IN THE TRUNCUS ANTERIOR AND ON THE RIGHT. A 24F GORE DRYSEAL SHEATH WAS INSERTED INTO THE RIGHT COMMON FEMORAL VEIN, AND A
Patient problems: Cardiac Arrest; Heart Failure/Congestive Heart Failure; Loss of consciousness; Low Blood Pressure/ Hypotension; Respiratory Arrest
MAUDE report 11682925 ↗InjuryFeb 17, 2021Improper or Incorrect Procedure or Method
A (B)(6) YEAR-OLD FEMALE PATIENT WITH CHRONIC PANCREATITIS PRESENTED TO THE EMERGENCY DEPARTMENT WITH HYPERTENSION AND SUSPECTED ACUTE MYOCARDIAL INFARCTION (MI). SHE WAS DIAGNOSED WITH A PULMONARY EMBOLISM (PE) AFTER UNDERGOING A RIGHT HEART CATHETERIZATION AND PULMONARY ANGIOGRAM (ACUTE MI WAS RULED OUT). ON (B)(6) 2021, THE INARI TRIEVER16 (T16), TRIEVER20 (T20), AND MEDIUM FLOWTRIEVER (FT) DISKS WERE USED TO ATTEMPT TO TREAT THE PE. THE PATIENT REMAINED HYPERTENSIVE AND TACHYCARDIC THROUGHOUT THE MECHANICAL THROMBECTOMY, WITH MARKEDLY ELEVATED RIGHT-SIDED PULMONARY AND ATRIAL PRESSURES. THE CLOT IN THE RIGHT PULMONARY ARTERY WAS SUCCESSFULLY ASPIRATED, BUT CLOT REMAINED IN THE LEFT LOWER LOBE (LLL) DESPITE USE OF THE T20, T16, AND MEDIUM FT DISKS. AN EKOS CATHETER WAS PLACED DUE TO THE PERSISTENT TACHYCARDIA, AND THE CASE WAS CONCLUDED. THE FOLLOWING DAY, RIGHT HEART CATHETERIZATION REVEALED RESOLUTION OF RIGHT VENTRICLE FAILURE AND NORMALIZATION OF RIGHT ATRIAL PRESSURE (~20 REDUCED TO ~6 MMHG). THE PATIENT'S TACHYCARDIA AND NAUSEA PERSISTED, AND THE HGB LEVEL DECREASED FROM 9 TO 7 GM/DL DUE TO 600 CC OF BLOOD BEING ASPIRATED DURING THE PROCEDURE. THE PATIENT WAS INFUSED WITH
Patient problems: Anemia; Hematoma; High Blood Pressure/ Hypertension; Hypovolemia
MAUDE report 11336298 ↗DeathJan 21, 2021Use of Device Problem; Use of Device Problem
A (B)(6)-YEAR-OLD FEMALE PATIENT WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE PRESENTED TO THE EMERGENCY DEPARTMENT WITH CHEST PAIN ON (B)(6) 2020. SHE WAS ADMITTED TO THE CATHETERIZATION LAB, WHERE SHE UNDERWENT PERCUTANEOUS CORONARY INTERVENTION AND RECEIVED 2 CORONARY STENTS. ON (B)(6) 2020, AS THE PATIENT WAS RECOVERING FROM THE PROCEDURE, SHE BEGAN EXPERIENCING CHEST PAIN WITH SHORTNESS OF BREATH. A CT ANGIOGRAM REVEALED A SADDLE PULMONARY EMBOLISM (PE) WITH BILATERAL CLOT BURDEN. ON (B)(6) 2020, THE INARI MEDICAL TRIEVER20 (T20), TRIEVER16 (T16), AND MEDIUM FLOWTRIEVER (FT) DISKS WERE USED TO ATTEMPT TO TREAT THE PE. PRIOR TO THE CASE, IT WAS NOTED THAT THE PATIENT HAD SOME RIGHT VENTRICLE STRAIN, ELEVATED TROPONIN LEVELS, AND A HEMOGLOBIN LEVEL OF OVER 12 G/DL. AS THE CASE BEGAN, THE PATIENT'S HEART RATE WAS BETWEEN 130-150 BPM, AND BLOOD PRESSURE WAS 152/72 MMHG. ACCESS WAS GAINED VIA THE RIGHT COMMON FEMORAL VEIN, AND A BENTSON WIRE AND ANGLED PIGTAIL CATHETER WERE USED TO SUCCESSFULLY CROSS THE HEART AND ADVANCE TO THE MAIN PULMONARY ARTERY (PA); THE PA PRESSURE WAS 54/30/14 MMHG. THE WIRE WAS THEN MANEUVERED TO THE RIGHT PA AND EXCHANGED FOR A BOSTON SCIENTIFIC AMPLATZ SUP
Patient problems: Cardiac Arrest; Hypovolemic Shock; Hypoxia; Loss of consciousness; Low Blood Pressure/ Hypotension; Oversedation; Respiratory Arrest
MAUDE report 11211496 ↗DeathJan 16, 2021Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method
THE FOLLOWING ADDITIONAL EVENT INFORMATION WAS PROVIDED TO INARI ON (B)(6), 2021. THE DAY BEFORE THE PROCEDURE, THE TEE DID NOT REVEAL ANY EVIDENCE OF A PERICARDIAL EFFUSION. ON THE DAY OF THE PROCEDURE, THE PATIENT WAS INTUBATED AND A SECOND TEE WAS PERFORMED, WHICH IDENTIFIED SOME SMALL PERICARDIAL EFFUSION; HOWEVER, THERE WAS NO SURGICAL PLAN TO TREAT AS IT WAS NOT BELIEVED TO BE SEVERE. AFTER THE CASE CONCLUDED AND THE COMPANY REPRESENTATIVE LEFT THE FACILITY, THE PATIENT EXPERIENCED WHAT WAS BELIEVED TO BE A REPERFUSION INJURY AND WAS STABILIZED ON A VENTILATOR. A BRONCHOSCOPY CONFIRMED NO SIGNS OF BLEEDING. THE PATIENT SUBSEQUENTLY DETERIORATED AND THE CAUSE OF DEATH WAS LISTED AS ACUTE SEVERE HYPOXIC RESPIRATORY FAILURE, ACUTE RIGHT VENTRICLE HEART FAILURE, AND CARDIOPULMONARY ARREST.
Patient problems: Hemoptysis; Hypovolemia; Low Blood Pressure/ Hypotension; Low Oxygen Saturation; Pericardial Effusion
MAUDE report 11182617 ↗InjuryJul 6, 2020Patient Device Interaction Problem; Patient Device Interaction Problem
A (B)(6)-YEAR-OLD MALE PATIENT WITH A HISTORY LUNG CANCER WITH PRIOR CHEST IRRADIATION PRESENTED TO THE HOSPITAL IN EARLY (B)(6) 2020 WITH SYMPTOMS OF A PULMONARY EMBOLISM (PE). HEPARIN WAS ADMINISTERED, BUT THE PATIENT WAS INELIGIBLE FOR THROMBOLYTIC THERAPY (BLEEDING RISK). COMPUTED TOMOGRAPHY ANGIOGRAPHY (CTA) REVEALED THE PATIENT HAD BILATERAL PE. THE BASELINE VITAL SIGNS WERE: HEART RATE 95 BPM, BLOOD PRESSURE 120/73, AND O2 SATURATION 95% ON A NON-REBREATHER MASK AT 6L O2. ON (B)(6) 2020, THE INARI TRIEVER20 (T20) WAS USED TO ATTEMPT TO TREAT THE BILATERAL PE. ULTRASOUND WAS USED TO GUIDE ACCESS TO THE RIGHT COMMON FEMORAL VEIN. AN 8 FR SHEATH WAS INSERTED OVER THE GUIDEWIRE, FOLLOWED BY AN ANGLED PIG TAIL CATHETER WHICH WAS USED TO CROSS THE RIGHT HEART TO OBTAIN PULMONARY ARTERY PRESSURE (36/18). THE PIG TAIL CATHETER WAS THEN EXCHANGED FOR A BOSTON SCIENTIFIC AMPLATZ SUPER STIFF GUIDEWIRE (260 CM), WHICH WAS ADVANCED TO THE LATERAL BRANCH OF THE LEFT LOWER LOBE. THE ACCESS SITE WAS THEN DILATED TO ACCOMMODATE A 22 FR GORE DRYSEAL SHEATH. FOLLOWING INSERTION OF THE GORE SHEATH, THE T20 WAS SUCCESSFULLY INSERTED AND ADVANCED TO THE LEFT PULMONARY ARTERY. A TOTAL OF 4 ASPIRAT
Patient problems: Vascular Dissection
MAUDE report 10237513 ↗InjuryMar 18, 2020Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method
A (B)(6)-YEAR-OLD FEMALE PATIENT WITH POST THROMBOTIC SYNDROME (PTS) AND CHRONIC THROMBOEMBOLIC PULMONARY HYPERTENSION (CTEPH) WITH A HISTORY OF PULMONARY EMBOLISM (PE) AND DEEP VEIN THROMBOSIS DEVELOPED A MASSIVE PE AFTER NON-COMPLIANCE WITH THE PRESCRIBED ANTICOAGULATION MEDICATION. THE PATIENT'S VITAL SIGNS WERE: HEART RATE 88-90 BPM, BLOOD PRESSURE 120/80 MMHG, AND BLOOD OXYGENATION SATURATION 97-98%. THE PATIENT WAS ADMITTED TO THE ICU ON (B)(6) 2020 AND ON (B)(6) 2020, INARI MEDICAL'S TRIEVER20 WAS USED TO TREAT THE PE. AFTER ACCESS WAS GAINED VIA A RIGHT TRANSFEMORAL APPROACH, AN ANGLED PIGTAIL CATHETER WAS PLACED IN THE PULMONARY ARTERY. HEMODYNAMIC MEASUREMENTS INCLUDED LEFT PULMONARY ARTERY (PA) PRESSURE OF 65/16/38 (SYSTOLIC, DIASTOLIC, MEAN) MMHG, MAIN PA MEASURED 63/6/32 MMHG, AND RIGHT PA 57/14/35 MMHG. A COOK MEDICAL BENTSON 0.035" GUIDEWIRE WAS PLACED DISTALLY IN THE LOWER RIGHT LOBE, TARGETING THROMBUS IN THE RIGHT PA. THE ACCESS SITE WAS UPSIZED TO A 22 FR GORE DRYSEAL TO ACCOMMODATE THE TRIEVER20, WHICH WAS THEN ADVANCED TO THE RIGHT LOBE BEYOND THE TARGETED CLOT (SADDLE WRAPPED AROUND THE TRUNCUS ANTERIOR). THE PULMONARY ANGIOGRAM REVEALED THE CLOT MOVED DISTALL
Patient problems: Low Blood Pressure/ Hypotension
MAUDE report 9849549 ↗
Other Inari Medical, Inc. products
All Inari Medical, Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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