VISTA BRITE TIPRecalls & reported problems across all models
Cordis Corporation · 26 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one VISTA BRITE TIP model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 59
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls
- 1
We found 26 models of VISTA BRITE TIP by Cordis Corporation in the FDA's device registry (GUDID). Together they are named in 59 adverse event reports in the FDA's MAUDE database, received between Oct 14, 2016 and Mar 26, 2026 — classified as 4 injuries, 55 malfunctions.
The most frequently reported specific device problem is “Crack” (18 reports).
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
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
VISTA BRITE TIP recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Feb 7, 2025Open, Classified
Catheter manufactured at the incorrect length.
Z-1330-2025 · Root cause: Employee error · Recall details · FDA record ↗
Most reported VISTA BRITE TIP problems
Device problems
- Crack18
- Detachment of Device or Device Component6
- Difficult to Remove6
- Material Puncture/Hole6
- Material Frayed5
- Material Split, Cut or Torn4
- Material Deformation3
- Break2
Patient problems
- No Clinical Signs, Symptoms or Conditions34
- No Consequences Or Impact To Patient12
- No Known Impact Or Consequence To Patient7
- Chest Pain3
- Dyspnea1
- Foreign Body In Patient1
- Insufficient Information1
- Nausea1
VISTA BRITE TIP models
26 models, most reported first. Each model has its own page with its reports, recalls and device details.
- VISTA BRITE TIP SM7504CATHETER, PERCUTANEOUS1 recall0 reports
- VISTA BRITE TIP 67005400CATHETER, PERCUTANEOUS22 reports
- VISTA BRITE TIP 67005200CATHETER, PERCUTANEOUS6 reports
- VISTA BRITE TIP 67008100CATHETER, PERCUTANEOUS3 reports
- VISTA BRITE TIP 67012600CATHETER, PERCUTANEOUS3 reports
- VISTA BRITE TIP 6700540ECATHETER, PERCUTANEOUS2 reports
- VISTA BRITE TIP 6700820ECATHETER, PERCUTANEOUS2 reports
- VISTA BRITE TIP 67005600CATHETER, PERCUTANEOUS2 reports
- VISTA BRITE TIP 67018000CATHETER, PERCUTANEOUS2 reports
- VISTA BRITE TIP 4037553RCATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 4038553ACATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 4038953SCATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 511040PCATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 67005300CATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 67008000CATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 6700820LCATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 67008400CATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 67013000CATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 67019055CATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 67027090CATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 77800400CATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 77803400CATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 77804500CATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 77805400CATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 77805800CATHETER, PERCUTANEOUS1 report
- VISTA BRITE TIP 77808200CATHETER, PERCUTANEOUS1 report
Recent VISTA BRITE TIP adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionMar 26, 2026Crack
AS REPORTED, PIECES OF THE HUBS OF A 6F INFINITI DIAGNOSTIC CATHETER AND A 6F VISTA BRITE TIP GUIDING CATHETER CONSISTENTLY BROKE OFF DURING THE PROCEDURE. THERE WAS NO REPORTED PATIENT INJURY. THE EXACT EVENT DATE IS UNKNOWN. MULTIPLE ATTEMPTS TO OBTAIN SUPPLEMENTAL INFORMATION WERE MADE; HOWEVER, ADDITIONAL EVENT DETAILS WERE NOT PROVIDED. THE DEVICES WERE RETURNED FOR EVALUATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24703719 ↗MalfunctionMar 2, 2026Leak/Splash
AS REPORTED, THE 6F .070 JR4 VISTA BRITE TIP CATHETER WAS COLLAPSED/LEAKING. THERE WAS NO REPORTED INJURY TO THE PATIENT. THE DEVICE WILL BE RETURNED FOR EVALUATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24483831 ↗MalfunctionJan 12, 2026Crack
AS REPORTED, THE LUER LOCK HUB OF A 6F .070-INCH EXTRA BACKUP (XB) 3.5 ECO PACK GUIDING CATHETER WAS DEFECTIVE OUT OF THE PACKAGE. THERE WAS NO REPORTED PATIENT INJURY. THE REPORTED ISSUE INVOLVED A GUIDING CATHETER THAT DID NOT APPEAR AS EXPECTED OUT OF THE PACKAGE. THE CUSTOMER WAS UNSURE HOW TO DESCRIBE THE DAMAGE AND NOTED THEY HAD NOT PERSONALLY SEEN THE CATHETER. THE INTENDED PROCEDURE WAS A LEFT CORONARY PERCUTANEOUS CORONARY INTERVENTION (PCI). ANOTHER EXTRA BACKUP (XB) 3.5 ECO PACK GUIDING CATHETER WAS USED TO COMPLETE THE PROCEDURE. THE DEVICE WAS STORED AND HANDLED ACCORDING TO THE INSTRUCTIONS FOR USE (IFU), AND THERE WAS NO DAMAGE OBSERVED PRIOR TO OPENING THE PACKAGE. THERE WERE NO ISSUES REMOVING THE DEVICE FROM THE STERILE PACKAGING, AND IT WAS PREPPED ACCORDING TO THE IFU WITHOUT DIFFICULTY. THE DEVICE WAS RETURNED FOR EVALUATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24046659 ↗InjuryJul 12, 2025Difficult to Remove; Difficult to Remove
AS REPORTED, DURING AN ANGIOGRAM PROCEDURE, A 6F JUDKINS RIGHT 4 (JR4) VISTA BRITE TIP GUIDING CATHETER BECAME KINKED AND THE PHYSICIAN WAS UNABLE TO REMOVE IT. IT WAS DETERMINED THAT THE PATIENT NEEDED A HIGHER LEVEL OF CARE AND WAS TRANSPORTED TO ANOTHER MEDICAL CENTER FOR ITS REMOVAL. THE PRODUCT WAS STORED AND HANDLED ACCORDING TO THE INSTRUCTIONS FOR USE (IFU), AND NO DAMAGE WAS NOTICED PRIOR TO OPENING THE PACKAGE. THERE WAS NO DIFFICULTY REMOVING THE DEVICE FROM THE STERILE PACKAGING. THE DEVICE WAS PREPPED ACCORDING TO THE IFU, AND NO ISSUES WERE EXPERIENCED DURING PREPARATION. IT IS NOT SPECIFIED WHETHER ANOTHER VISTA BRITE TIP WAS USED TO COMPLETE THE PROCEDURE. THE DEVICE IS EXPECTED TO BE RETURNED FOR EVALUATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22488900 ↗MalfunctionApr 17, 2025Crack; Crack
AS REPORTED, THE DISTAL TIP OF A 6F 100CM JUDKINS RIGHT (JR) 3.5 VISTA BRITE TIP GUIDING CATHETER WAS FOUND TO BE FRACTURED DURING PREPARATION. THE CATHETER TIP FRACTURED BUT REMAINED ATTACHED TO THE CATHETER. A NON-CORDIS GUIDING CATHETER WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO REPORTED INJURIES TO THE PATIENT AND NO SIGNS OF INFECTIOUS DISEASE. THIS WAS DURING A PERCUTANEOUS CORONARY INTERVENTION (PCI) PROCEDURE IN WHICH ANGIOGRAPHY REVEALED A GREATER THAN 80% STENOSIS OF THE LEFT ANTERIOR DESCENDING (LAD) CORONARY ARTERY. THE VESSEL CHARACTERISTICS AT THE TARGET SITE INCLUDED BIFURCATION, MILD CALCIFICATION, AND MILD TORTUOSITY. THE OPERATOR HAD BEEN TRAINED. THE DEVICE WAS STORED AND PREPPED PER THE INSTRUCTION FOR USE (IFU). THE CATHETER DID NOT BECOME ENTRAPPED AT ANY POINT IN THE PROCEDURE AS THE DEFECT WAS FOUND DURING PREPARATION. THE DEVICE WILL BE RETURNED FOR EVALUATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21854822 ↗MalfunctionSep 1, 2023Crack; Crack
AS REPORTED, A 6F .070 XB 3.5 100CM VISTA BRITE TIP WAS FOUND WITH A ¿COMPRESSION FRACTURE¿ IN THE DISTAL FIRST BEND WHEN THE PACKAGING WAS OPENED. THE CATHETER WAS REPLACED AND THE PROCEDURE COMPLETED. THERE WAS NO REPORTED PATIENT INJURY. THE DEVICE WAS USED IN AN INTERVENTIONAL PROCEDURE FOR THE LEFT CORONARY ARTERY (LCA). THE LCA HAD MILD CALCIFICATION, MILD TORTUOSITY AND A 90% STENOSIS. THE VESSEL DID NOT HAVE AN ACUTE ANGLE OR BIFURCATION. THE DEVICE WAS NOT USED FOR TREATMENT OF A CHRONIC TOTAL OCCLUSION. THE DEVICE WAS NOT INSPECTED PRIOR TO OPENING THE PACKAGE. THE DEVICE WAS STORED AND PREPPED PER THE INSTRUCTIONS FOR USE (IFU). THE USER IS TRAINED TO THE DEVICE. OTHER PROCEDURAL DETAILS WERE REQUESTED BUT ARE UNKNOWN, UNAVAILABLE, NOT ANSWERED, OR NOT APPLICABLE. THE DEVICE WILL BE RETURNED FOR EVALUATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17671470 ↗MalfunctionAug 11, 2023Material Frayed; Material Split, Cut or Torn; Material Frayed; Material Split, Cut or Torn
AS REPORTED, THE BRITE TIP OF A 6F .070 XB 3 100 CM VISTA BRITE TIP GUIDING CATHETER WAS FOUND TO BE FRAYED DURING PREP. THE DEVICE WAS NOT USED INSIDE THE PATIENT. IT WAS REPLACED WITH ANOTHER UNKNOWN GUIDING CATHETER TO COMPLETE THE PROCEDURE. THIS INCIDENT HAD NO EFFECT ON THE PATIENT. THE DEVICE WAS NOT PULLED FROM THE PACKAGING BY THE HUB. THE DEVICE WAS NOT TORQUED OR ¿STEERED¿ BY THE HUB. THE DEVICE DAMAGE WAS NOT FRAYED INTO TWO SEPARATE PIECES. THE TARGET SITE VESSEL CHARACTERISTICS WERE MILD CALCIFICATION, NO TORTUOSITY, 80% STENOSIS, NO ACUTE ANGLE AND YES BIFURCATING. THE ACCESS SITE WAS THE RADIAL ARTERY, AND THE CHARACTERISTICS WERE NO CALCIUM, TORTUOSITY, STENOSIS, ACUTE ANGLE OR BIFURCATING. ANGIOGRAPHY REVEALED MORE THAN 80% STENOSIS OF THE LEFT ANTERIOR DESCENDING CORONARY BRANCH, WHICH REQUIRED PERCUTANEOUS CORONARY INTERVENTION (PCI). A CONTRALATERAL APPROACH WAS NOT USED. THE OPERATOR HAD BEEN TRAINED. THE PATIENT HAS A HISTORY OF CORONARY ARTERY DISEASE WHO WAS ADMITTED TO THE HOSPITAL WITH ANTERIOR CARDIAC PAIN. THE PATIENT HAS NO INFECTIOUS DISEASES. THE DEVICE WILL BE RETURNED FOR EVALUATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17508688 ↗MalfunctionAug 3, 2023Crack; Crack
AS REPORTED, THE BODY SHAFT OF A 7F VISTA BRITE TIP EXTRA BACK-UP 4.5 GUIDING CATHETER WAS FOUND FRACTURED DURING USE IN A PERCUTANEOUS CORONARY INTERVENTION (PCI) PROCEDURE. THERE WAS NO REPORTED PATIENT INJURY. THE OPERATOR HAS EXTENSIVE CLINICAL SURGICAL EXPERIENCE. THE PRODUCT WAS STORED, HANDLED, INSPECTED AND PREPPED ACCORDING TO THE INSTRUCTIONS FOR USE (IFU). THERE WAS NO DIFFICULTY EXPERIENCED IN PREPPING THE DEVICE. THE TIP OF THE DEVICE WAS VISIBLE UNDER FLUOROSCOPY THROUGHOUT THE PROCEDURE. ADDITIONAL EVENT DETAILS WERE REQUESTED; HOWEVER, NOT PROVIDED. THE DEVICE IS EXPECTED TO BE RETURNED FOR EVALUATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17455504 ↗MalfunctionAug 3, 2023Crack; Crack
AS REPORTED, THE 7F VISTA BRITE TIP JUDKINS LEFT 4 GUIDING CATHETER FRACTURED DURING USE IN A PERCUTANEOUS CORONARY INTERVENTION (PCI) PROCEDURE. THERE WAS NO REPORTED PATIENT INJURY. THE PRODUCT WAS STORED, HANDLED, INSPECTED, AND PREPPED ACCORDING TO THE INSTRUCTIONS FOR USE (IFU). THERE WERE NO ANOMALIES NOTED WHEN THE PRODUCT WAS REMOVED FROM THE PACKAGING. THE TIP WAS VISIBLE UNDER FLUOROSCOPY THROUGHOUT THE PROCEDURE. ADDITIONAL EVENT DETAILS WERE REQUESTED; HOWEVER, NOT PROVIDED. THE DEVICE IS EXPECTED TO BE RETURNED FOR EVALUATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17455376 ↗MalfunctionJul 31, 2023Crack; Difficult to Remove; Crack; Difficult to Remove
AS REPORTED, DURING AN EMERGENT CARDIAC CATHETERIZATION TO TREAT A PATIENT FOR HEART ATTACK, A 6F 100CM JUDKINS RIGHT (JR) 3.5 2 SIDE-HOLE VISTA BRITE TIP GUIDING CATHETER BECAME COILED INSIDE OF THE PATIENT¿S ARTERY WHILE ATTEMPTING TO TORQUE THE DEVICE. THIS MADE IT DIFFICULT TO MANEUVER THE CATHETER. RESISTANCE WAS EXPERIENCED WHILE WITHDRAWING THE DEVICE AND THE DISTAL CATHETER WAS FRACTURED UPON REMOVAL. AN UNKNOWN 6F CATHETER SHEATH INTRODUCER (CSI), WHICH WAS INSERTED FROM THE RIGHT FEMORAL ARTERY, WAS THEN EXCHANGED FOR A 7F 45CM BRITE TIP CSI WHICH WAS ABLE TO ADLE TO ADVANCE TORTUOUSLY. A NEW 6F 100CM JR 3.5 VISTA BRITE TIP GUIDING CATHETER WAS THEN INSERTED; HOWEVER, THE SAME ISSUE OCCURRED WHERE THE DEVICE WAS COILED UPON TORQUING, THERE WAS DIFFICULTY REMOVING THE DEVICE, AND THE DISTAL CATHETER WAS FRACTURED. AS A RESULT, THE ACCESS SITE WAS SWITCHED TO THE LEFT FEMORAL ARTERY AND THE 7F 45CM BRITE TIP CSI WAS INSERTED. THE RIGHT CORONARY ARTERY (RCA) WAS CANNULATED, AND A NON-CORDIS .014 GUIDEWIRE WAS ADVANCED TO THE DISTAL PORTION OF THE VESSEL. A PROXIMAL SEGMENT LESION WAS CONFIRMED AND A THROMBECTOMY WAS PERFORMED WITH THE CLOTS DESCRIBED AS ¿ABUNDANT¿. A NON-COR
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17424078 ↗MalfunctionJul 31, 2023Crack; Difficult to Remove; Crack; Difficult to Remove
AS REPORTED, DURING AN EMERGENT CARDIAC CATHETERIZATION TO TREAT A PATIENT FOR HEART ATTACK, A 6F 100CM JUDKINS RIGHT (JR) 3.5 2 SIDE-HOLE VISTA BRITE TIP GUIDING CATHETER BECAME COILED INSIDE OF THE PATIENT¿S ARTERY WHILE ATTEMPTING TO TORQUE THE DEVICE. THIS MADE IT DIFFICULT TO MANEUVER THE CATHETER. RESISTANCE WAS EXPERIENCED WHILE WITHDRAWING THE DEVICE AND THE DISTAL CATHETER WAS FRACTURED UPON REMOVAL. AN UNKNOWN 6F CATHETER SHEATH INTRODUCER (CSI), WHICH WAS INSERTED FROM THE RIGHT FEMORAL ARTERY, WAS THEN EXCHANGED FOR A 7F 45CM BRITE TIP CSI WHICH WAS ABLE TO ADLE TO ADVANCE TORTUOUSLY. A NEW 6F 100CM JR 3.5 VISTA BRITE TIP GUIDING CATHETER WAS THEN INSERTED; HOWEVER, THE SAME ISSUE OCCURRED WHERE THE DEVICE WAS COILED UPON TORQUING, THERE WAS DIFFICULTY REMOVING THE DEVICE, AND THE DISTAL CATHETER WAS FRACTURED. AS A RESULT, THE ACCESS SITE WAS SWITCHED TO THE LEFT FEMORAL ARTERY AND THE 7F 45CM BRITE TIP CSI WAS INSERTED. THE RIGHT CORONARY ARTERY (RCA) WAS CANNULATED, AND A NON-CORDIS .014 GUIDEWIRE WAS ADVANCED TO THE DISTAL PORTION OF THE VESSEL. A PROXIMAL SEGMENT LESION WAS CONFIRMED AND A THROMBECTOMY WAS PERFORMED WITH THE CLOTS DESCRIBED AS ¿ABUNDANT¿. A NON-COR
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17424005 ↗MalfunctionMay 30, 2023Crack; Crack
AS REPORTED, THERE WAS A CRACK ON THE HUB OF A 6F .070 EXTRA BACK-UP (XB) 3.5 X 100CM VISTA BRITE TIP GUIDING CATHETER. THERE WERE NO REPORTS OF PATIENT INJURY. THE STAFF HAD DISCOVERED THE DEFECT AND HAD PRESENTED IT TO THE PHYSICIAN. THE DEVICE WILL BE RETURNED FOR EVALUATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17022178 ↗MalfunctionMay 10, 2023Crack; Crack
AS REPORTED, THE BRITE TIP/DISTAL TIP OF A 6F VISTA BRITE TIP XB 3.5 GUIDING CATHETER WAS FOUND FRACTURED. THE DEVICE DID NOT FRACTURE INTO TWO OR MORE PIECES. THE PROCEDURE WAS COMPLETED WITH A DIFFERENT UNKNOWN GUIDING CATHETER. THIS EVENT HAD NO EFFECT ON THE PATIENT. THERE WAS NO REPORTED PATIENT INJURY. THE DEVICE WAS PULLED FROM THE PACKAGING BY THE HUB. THE DEVICE WAS NOT TORQUED OR ¿STEERED¿ BY THE HUB. THE PATIENT HAS A PREVIOUS HISTORY OF CORONARY ARTERY DISEASE WHO WAS ADMITTED WITH ANTERIOR HEART PAIN. THE TARGET SITE WAS MODERATELY CALCIFIED AND WITH MILD TORTUOSITY. THE STENOSIS PERCENTAGE WAS 80%. THERE WAS NO ACUTE ANGLE OR BIFURCATING. THE ACCESS SITE DID NOT HAVE CALCIUM OR TORTUOSITY. THE ACCESS SITE DID NOT HAVE STENOSIS, ACUTE ANGLE, OR BIFURCATION. AN UNKNOWN CORDIS SHEATH WAS USED. THE ANGIOGRAPHY REVEALED MORE THAN 80% STENOSIS OF THE ANTERIOR DESCENDING BRANCH OF THE LEFT CORONARY REQUIRING A PERCUTANEOUS CORONARY INTERVENTION (PCI) AND A CONTRALATERAL APPROACH WAS NOT USED. THE OPERATOR HAD BEEN TRAINED TO USE OUR XB 3.5 GUIDING CATHETER. OTHER PROCEDURAL DETAILS WERE REQUESTED BUT ARE UNKNOWN, UNAVAILABLE, NOT ANSWERED, OR NOT APPLICABLE. THE DEVICE WILL
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16903309 ↗MalfunctionMay 5, 2023Crack; Crack
AS REPORTED, A 6F .070 XB 4 100CM VISTA BRITE TIP GUIDING CATHETER WAS FOUND FRACTURED IN THE MEDIAL SEGMENT DURING PREP. THE DEVICE WAS NOT USED IN THE PATIENT. ANOTHER 6F VISTA BRITE TIP XB4 CATHETER WAS USED TO COMPLETE THE PROCEDURE. THERE WAS NO REPORTED PATIENT INJURY. THE PRODUCT WAS STORED AND HANDLED ACCORDING TO THE INSTRUCTIONS FOR USE (IFU). THERE WAS NO DEVICE DAMAGE NOTICED PRIOR TO OPENING THE PACKAGE. THE DEVICE WAS PREPPED PER THE INSTRUCTIONS FOR USE (IFU) AND THERE WAS NO DIFFICULTY EXPERIENCED IN PREPPING THE DEVICE. NEITHER THE PRODUCT NOR ANY OR ANY OF THE OTHER DEVICES USED WITH IT HAD BEEN RE-STERILIZED. MULTIPLE ATTEMPTS WERE MADE TO OBTAIN THE RETURN STATUS OF THE DEVICE; HOWEVER, THE DEVICE WAS NOT RETURNED FOR EVALUATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16879688 ↗MalfunctionMar 16, 2023Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
AS REPORTED, A HAIR WAS FOUND IN THE INNER PACKAGE OF 6F .070 EXTRA BACK-UP RIGHT CA 100CM VISTA BRITE TIP GUIDING CATHETER WHEN IT WAS DELIVERED TO THE HOSPITAL. THEREFORE, MAKING IT UNUSABLE. THERE WAS NO REPORTED PATIENT INJURY. THE DEVICE WILL BE RETURNED FOR EVALUATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16554762 ↗
Other Cordis Corporation products
All Cordis Corporation 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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