COOK G60344Recalls & reported problems
William A. Cook Australia Pty. Ltd. · Zenith Iliac Branch · Class 3 · Implant
All models of Cook (11)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00827002603448), received between Jun 1, 2026 and Jun 1, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Device Endoleak” (1 report).
111 other recalls cover devices cleared under the same FDA submission (P020018); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Device Endoleak1
Patient problems
- Clinical Endoleak1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 1, 2026Device Endoleak
AS REPORTED PER COMPLAINT EMAIL: "GOOD AFTERNOON. I AM ONCE AGAIN REPORTING MORE FABRIC LEAKS FROM (REDACTED) ENDOGRAFTS. THESE WERE PICKED UP ON FOLLOW UP SCAN TODAY WITH THE SURGEON. THE CASE WAS ORIGINALLY PERFORMED ON (REDACTED). THE ENDOLEAK IS REPORTED TO HAVE PERSISTED FROM THE LIMBS AND (REDACTED) DEVICES." FURTHER INFORMATION PROVIDED STATED: THE PHYSICIAN ATTRIBUTED THE CAUSE TO A FABRIC LEAK IN THE DEVICE. NO PRE-EXISTING ANATOMICAL CONDITIONS (SUCH AS VESSEL CALCIFICATION OR TORTUOSITY) WERE IDENTIFIED, AND NO DIFFICULTIES WERE ENCOUNTERED DURING THE ORIGINAL DEPLOYMENT. TO TREAT THE ENDOLEAK, A 16MM GRAFT WAS USED TO RELINE THE AFFECTED AREA, AND ADDITIONAL GRAFTS WERE ALSO IMPLANTED AS ADJUNCTIVE MEASURES. NO HIGH BLOOD PRESSURE OR GRAFT OBSTRUCTION WAS OBSERVED DURING THE ENDOLEAK EVENT. THE IMPLANTED DEVICES WERE NOT AVAILABLE FOR RETURN. THE PATIENT CONTINUED TO BE MONITORED FOLLOWING THE INTERVENTION, WITH NO FURTHER ADVERSE OUTCOME NOTED AT THE TIME OF REPORTING.
Patient problems: Clinical Endoleak
MAUDE report 25354515 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under P020018. One submission often covers many models, so check the product and lot details in each record.
- Z-3138-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Main Body, REF TFFB-36-95-ZT, REF G48432, 22 Fr ID/ 8.5 mm OD, Sterile.
- Z-3134-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Main Body, REF TFFB-28-96-ZT, REF G48418, 20 Fr ID/ 7.7 mm OD, Sterile
- Z-3137-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Main Body, REF TFFB-32-96-ZT, REF G48428, 20 Fr ID/ 7.7 mm OD, Sterile.
- Z-3150-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Iliac Leg, REF TFLE-20-56-ZT, REF G48473, 16Fr ID/ 6.0 mm OD, Sterile.
- Z-3143-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Iliac Leg, REF TFLE-16-73-ZT, REF G48462, 16Fr ID/ 6.0 mm OD, Sterile.
- Z-3131-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Main Body, REF TFFB-24-96-ZT, REF G48408, 18 Fr ID/ 7.1 mm OD, Sterile
- Z-3158-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Main Body Extension, REF ESBE-32-39, REF G32184, 20 Fr. ID/ 7.7 mm OD, Sterile.
- Z-3144-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Iliac Leg, REF TFLE-16-90-ZT, REF G48463, 16Fr ID/ 6.0 mm OD, Sterile.
- Z-3135-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Main Body, REF TFFB-30-82-ZT, REF G48422, 20 Fr ID/ 7.7 mm OD
- Z-3156-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Main Body Extension, REF ESBE-22-29, REF G32179, 18 Fr. ID/ 6.90 OD, Sterile.
- Z-3155-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Iliac Leg, REF TFLE-24-90-ZT, REF G48479, 16 Fr. ID/ 6.0 OD, Sterile.
- Z-3136-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Main Body, REF TFFB-32-82-ZT, REF G48427, 20 Fr ID/ 7.7 mm OD, Sterile.
- Z-3130-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Main Body, REF TFFB-24-82-ZT, REF G48407, 18 Fr ID/ 7.1 mm OD, Sterile
- Z-3132-2011 · Apr 15, 2011 · TerminatedCook Medical, Zenith Flex AAA Endovascular Graft Main Body, REF TFFB-26-96-ZT, REF G48413, 18 Fr ID/ 7.1 mm OD, Sterile.
- Z-3152-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Iliac Leg, REF TFLE-20-73-ZT, REF G48476, 16Fr ID/ 6.0 mm OD, Sterile.
…and 96 more.
Other SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT devices
- Endurant® IIs ESBF2814C103EMedtronic, Inc. · SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT2 recalls34 deaths254 reports
- Endurant® IIs ESBF3214C103EMedtronic, Inc. · SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT2 recalls19 deaths173 reports
- Endurant® IIs ESBF3614C103EMedtronic, Inc. · SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 recall37 deaths214 reports
- Endurant® IIs ESBF2514C103EMedtronic, Inc. · SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT2 recalls18 deaths136 reports
- Endurant® IIs ESBF2314C103EMedtronic, Inc. · SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT2 recalls9 deaths60 reports
- RelayPro Thoracic Stent-Graft System 28-N4-34-154-34UBolton Medical Inc. · System, Endovascular Graft, Aortic Aneurysm Treatment3 recalls7 reports
- Vela Proximal Endograft System A34-34/C100-O20 VEndologix LLC · System, Endovascular Graft, Aortic Aneurysm Treatment3 deaths152 reports
- Endurant® II ETCF2828C49EMedtronic, Inc. · SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT2 recalls7 deaths44 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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