Zenith G32501Recalls & reported problems
William A. Cook Australia Pty. Ltd. · Zenith Fenestrated, AAA Endovascular Graft, Distal Body · Class 3 · Implant
All models of Zenith (32)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10827002325019), received between Feb 18, 2018 and Jun 2, 2019 — classified as 2 injuries.
The most frequently reported specific device problem is “Fluid/Blood Leak” (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.
Most reported problems
Device problems
- Fluid/Blood Leak1
- Leak/Splash1
Patient problems
- Hemorrhage/Blood Loss/Bleeding2
- Abdominal Pain1
- Low Blood Pressure/ Hypotension1
- Rupture1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJun 2, 2019Leak/Splash
ORIGINAL IMPLANT WAS ON (B)(6) 2016. SUCCESSFUL OUTCOME WITH NO LEAK DURING FINAL IMAGING. PATIENT WAS SEEN IN (B)(6) 2018 WHERE COMPUTERIZED TOMOGRAPHY (CT) WAS PERFORMED AND NO LEAK WAS DISCOVERED. ON (B)(6) 2019, PATIENT CAME TO HOSPITAL COMPLAINING OF ABDOMINAL PAIN. CT SHOWED BLOOD IN THE RETROPERITONEUM COMING FROM TYPE 3 ENDOLEAK. THE LEAK WAS LOCATED AROUND THE DISTAL BIFURCATED STENT GRAFT. THE LEAK WAS REPAIRED BY RELINING WITH GORE STENT GRAFT. FINAL IMAGING SHOWED NO LEAK. SOME ILIAC CALCIFICATION AND TORTUOSITY WAS NOTED.
Patient problems: Abdominal Pain; Hemorrhage/Blood Loss/Bleeding
MAUDE report 8661390 ↗InjuryFeb 18, 2018Fluid/Blood Leak
THE PROXIMAL AND DISTAL COMPONENTS LOST THEIR OVERLAP CREATING A TYPE 3 ENDOLEAK. THE PATIENT'S ANEURYSM RUPTURED AND PATIENT BECAME HYPOTENSIVE. THE PROXIMAL AND DISTAL COMPONENTS WERE REALIGNED WITH AN ADDITIONAL GRAFT. THE DISCONNECT JUNCTURE POINT WAS STRADDLED WITH THE JUNCTURE PIECE AND THE LEAK WAS SEALED. THE PATIENT REQUIRED BLOOD PERFUSION.
Patient problems: Hemorrhage/Blood Loss/Bleeding; Low Blood Pressure/ Hypotension; Rupture
MAUDE report 7279562 ↗
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-3140-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Iliac Leg, REF TFLE-12-56-ZT, REF G48449, 16Fr ID/ 6.0 mm OD, Sterile.
- Z-3145-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Iliac Leg, REF TFLE-18-56-ZT, REF G48465, 16Fr ID/ 6.0 mm 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-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-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.
- 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-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-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-3141-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Iliac Leg, REF TFLE-14-56-ZT, REF G48455, 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-3151-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Iliac Leg, REF TFLE-22-73-ZT, REF G48474, 16Fr ID/ 6.0 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-3146-2011 · Apr 15, 2011 · TerminatedCook Medical Zenith Flex AAA Endovascular Graft Iliac Leg, REF TFLE-18-73-ZT, REF G48466, 16Fr ID/ 6.0 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-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.
…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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