Z-2964-2020Class II

Zenith Alpha Abdominal Endovascular Graft - Distributed OUS only. Indicated for the endovascular treatment of...

Name: Z-2964-2020 Zenith Alpha Abdominal Endovascular Graft - Distributed OUS only. Indicated for the endovascular treatment of...
Creator: Cook Inc.
Published: 2020-08-11
License: https://open.fda.gov/license/

Cook Incorporated / initiated 2020-08-11 / Terminated / root cause: labeling and UDI

FDA source

Cook Inc. began a recall of Zenith Alpha Abdominal Endovascular Graft - Distributed OUS only. Indicated for the endovascular treatment of patients with abdominal aortic or aorto-iliac... on 2020-08-11. FDA classified it as Class II and gives the reason as "May contain excess glue within the handle of the delivery system, resulting in an inability to fully deploy the graft via the standard method or troubleshooting deployment method provided in the IFU". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as labeling and UDI.

Recall record

Recall number: Z-2964-2020
Classification: Class II
Status: Terminated
Initiated: 2020-08-11
Posted: 2020-09-12
Terminated: 2021-07-28
Recalling firm: Cook Incorporated
Product: Zenith Alpha Abdominal Endovascular Graft - Distributed OUS only. Indicated for the endovascular treatment of patients with abdominal aortic or aorto-iliac aneurysms Reference Part Number (RPN): ZIMB-22-108 ZIMB-22-118 ZIMB-22-128 ZIMB-22-70 ZIMB-22-84 ZIMB-22-98 ZIMB-24-108 ZIMB-24-118 ZIMB-24-128 ZIMB-24-70 ZIMB-24-84 ZIMB-24-98 ZIMB-26-108 ZIMB-26-118 ZIMB-26-128 ZIMB-26-70 ZIMB-26-84 ZIMB-26-98 ZIMB-28-108 ZIMB-28-118 ZIMB-28-128 ZIMB-28-70 ZIMB-28-84 ZIMB-28-98 ZIMB-30-108 ZIMB-30-118 ZIMB-30-128 ZIMB-30-70 ZIMB-30-84 ZIMB-30-98 ZIMB-32-108 ZIMB-32-108 ZIMB-32-118 ZIMB-32-128 ZIMB-32-70 ZIMB-32-84 ZIMB-32-98 ZIMB-36-108 ZIMB-36-118 ZIMB-36-128 ZIMB-36-84 ZIMB-36-98
Product code: MIH System, Endovascular Graft, Aortic Aneurysm Treatment
Reason for recall: May contain excess glue within the handle of the delivery system, resulting in an inability to fully deploy the graft via the standard method or troubleshooting deployment method provided in the IFU
Root cause tag: labeling and UDI
FDA root cause: Under Investigation by firm
Action: Cook Medical issued Urgent Medical Device Recall Dated 8/11/20 either mailed via courier or emailed to consignees stating reason for recall, health risk and action to take: Examine inventory immediately to determine if you have affected product(s) and quarantine any affected product that remains unused. Immediately cease all distribution and use of this product. 2. Return the affected product(s) to Cook Medical with a copy of the Acknowledgement and Receipt Form to receive a product credit. Refer to the Acknowledgement and Receipt Form for return instructions. Note: Unaffected products that are returned will not be credited. 3. Please complete the Acknowledgement and Receipt Form within 5 business days of receiving this letter. Even if you do not have affected product(s) on hand, you must still complete the Acknowledgement and Receipt Form and return via fax (812.339.7316) or email [email protected]). This notice must be shared with appropriate personnel, including down to the user level, within your organization or with any organization where the potentially affected devices have been transferred. 5. Immediately report adverse events to Cook Medical Customer Relations by phone at 800.457.4500 or 812.339.2235, Monday through Friday between 7:30am and 5:00pm (Eastern Time), or by email to: [email protected].
Quantity in commerce: 684 units
Distribution: Foreign Only: Canada SWEDEN AUSTRIA Belgium CZECH REPUBLIC DENMARK ESPA¿A FINLAND France GERMANY GREECE HUNGARY IRELAND ISRAEL Italia Nederland NORWAY POLAND PORTUGAL REUNION SERBIA SLOVENIA SOUTH AFRICA SWEDEN UNITED ARAB EMIRATES UNITED KINGDOM AUSTRALIA Hong Kong JAPAN NEW CALEDONIA New Zealand Thailand
Product codes and lots: Reference Part / Lot Numbers : ZIMB-22-108 9182141, 9983461, 10010790, 10136649, 13023971; ZIMB-22-118 10077065; ZIMB-22-70 9170948, 9196501, 9196502, 9311502, 9415647, 10156546, 10275239, 10337923; ZIMB-22-84 9100087, 9100089, 9118160, 9124830, 9132423, 9182145, 9403140, 9415636, 9415637, 9964029,9964055, 9974798, 9974799, 10153964,10153965, 10337925; ZIMB-22-98 9108371, 9163902, 9406786, 10136631, 10275243; ZIMB-24-108 9338301, 9854089, 9936720, 9936722, 9939734, 9939736, 9945749, 9945751, 9945753, 10318498; ZIMB-24-118 9100111, 9163853, 9959252, 9995361, 9999386, 10275245; ZIMB-24-128 9136557; ZIMB-24-70 9084499, 9118179, 9118180, 9163859, 9184781, 9196487, 9196590, 9300915, 9311508, 9338304,9978260, 9978261, 9983464, 10291632,13023978; ZIMB-24-84 9084507, 9118182, 9118183, 9118406, 9118409, 9163906, 9181250, 9196491, 9196593, 9279116, 9292346, 9321079, 9321083, 9324519, 9324521,9330492, 9330493, 9338306, 9365311, 9409601, 9409602, 9409604, 9959219, 9964025, 9964027,9964028, 9983471, 10017280, 10044210,10141902, 10141911, 10175395, 10175409, 10291637, 10291638, 10305523, 10305524,10332829, 10340274, 10340279, 13008932,13011201, 13020521, 13035543, 13041249,10056663XX, NS9088555; ZIMB-24-98 9076897, 9080500, 9080501, 9084510, 9084512, 9100134, 9100135, 9102515, 9118415, 9173828, 9321095, 9365312, 9373635, 9415651, 9964064,9969873, 9974816, 10052850, 10077067, 10098962, 10151099, 10186652, 13041251; ZIMB-26-108 9100142, 9163915, 9373477, 9904753, 9915021, 9930826, 9936725, 9936733, 9936734, 9953748, 10010796, 10010836, 10025525, 10108021,10175397, 10299712, 10309872, 13023989, 13023990; ZIMB-26-118 9286115, 10105275, 10299413, 13011587,13023992; ZIMB-26-70 9100151, 9217933, 9373479, 9373646, 9419035, 9425597, 9425598, 9915028, 9915029, 9915030,9995377, 9999389, 10025531, 10077068,13011591, 13015424, 13021170, 13023993, 13027639; ZIMB-26-84 9076909, 9076928, 9088530, 9118164, 9124843, 9196498, 9303243, 9303253, 9314216, 9321168, 9415652, 9415653, 9936744, 9978265, 10010848,10025534, 10130408, 10130411, 10139153, 10153985, 10225101, 10227951, 10282883,10331451, 13008934, 13008935, 13011595,13023997, 13030103, 13035545, 13035546,13035549, 13090261, 10139146X; ZIMB-26-98 9076932, 9088524, 9100103, 9108359, 9124922, 9170952, 9170972, 9181256, 9209904, 9307498,9307687, 9307688, 9321171, 9321173, 9376513,9376514, 9376516, 9425605, 9425607, 9978273, 9999333, 10017283, 10056684, 10105282,10113546, 10144804, 10153990, 10153991,10153992, 10227946, 10231315, 10309875,10331463, 10331489, 10331490, 13011600,13015425, 13027049, 13090267; ZIMB-28-108 9040730, 9869684, 9920813, 9920814, 9920817, 9951131, 9969884, 9969885, 9983493, 9999335,10022608, 10044216, 10056686, 10108037,10307420, 10332830, 13010195, 13011603, 13044015, 13188317; ZIMB-28-118 9064897, 9303288, 9412815, 9415641, 9425608, 9923193, 9969889, 10010800, 10031214,10047286, 13011606, 13041262 ZIMB-28-128 9193964, 9383486, 9915023, 9971444, 9974773, 10119913, 10119918, 10305544, 13027650; ZIMB-28-70 9037693, 9056000, 9064899, 9064901, 9088565, 9167748, 9212286, 9217990, 9226370, 9307689,9330495, 9330496, 9331479, 9338361, 9338362,9415633, 9415638, 9415643, 9425610, 9425613, 9930818, 9964070, 9966894, 10037025,10139135, 10139159, 10283657; ZIMB-28-84 9046402, 9136667, 9167751, 9190117, 9193974, 9212287, 9217995, 9226355, 9279120, 9303293,9303294, 9311539, 9314218, 9324565, 9324566,9324569, 9376519, 9383491, 9383496, 9415665, 9423252, 9425615, 9425636, 9425640, 9909088,9911870, 9948685, 9948691, 9966896, 9966900,9969905, 9986400, 9999343, 10022614,10022616, 10044217, 10044219, 10047287,10051143, 10052841, 10052868, 10068425, 10105284, 10154429, 10175398, 10175399,10271375, 10288149, 10297330, 10325658,10337931, 13010196, 13011613, 13021173,13027655, 13050699, 13101560, 10141924X; ZIMB-28-98 9037752, 9046415, 9055991, 9064922, 9124929, 9124932, 9136670, 9143825, 9218000, 9234946,9283231, 9373486, 9373488, 9376523, 9383415,9383501, 9425633, 9911865, 9911867, 9913326, 9913327, 9920819, 9920820, 9948687, 9948692,9956372, 9982267, 10007633, 10059719,10059720, 10136638, 10332808, 13008942, 13010340, 13021175, 13021177, 13078502,13101562; ZIMB-30-108 9212304, 9307494, 9307701, 9361542, 9904221, 9911853, 9911860, 9966907, 9969909, 9978296,9982268, 9999348, 10013746, 10129802,10156556, 10223556, 13078507, 13078509, 9904230X, NS9218007; ZIMB-30-118 9040636, 9056086, 9415666, 9959246, 9999350, 10001828, 10013748, 10132963, 10156542, 10156558, 10163202; ZIMB-30-128 9136542, 9283236, 9307703, 10047290,10156560, 13020527, 13199408; ZIMB-30-70 9423255, 9904219, 9992839, 10007637, 10007638, 10037030, 10156561, 10327926,13012746, 9933334X; ZIMB-30-84 9053445, 9056095, 9060405, 9150335, 9185031, 9185032, 9185034, 9190254, 9292350, 9292355, 9334354, 9338287, 9404792, 9426588, 9930856, 9971412, 9971451, 10044221, 10051128, 10059685, 10098974, 10156565, 10156567, 10315171, 10315172, 13030115, 13030117, 13050689, 13094868; ZIMB-30-98 9037765, 9060395, 9060412, 9060414, 9193801, 9206515, 9212249, 9242441, 9933350, 9974777, 9982278, 9986414, 10007647, 10017296, 10037041, 10062767, 10062768, 10062770, 10119927, 10119928, 10119929, 10136643, 10156538, 10271379, 10315173, 10331468, 10343161, 13030124, 13032866, 13078512, 13105397, 10052870X ZIMB-32-108 9034048, 9060448, 9159951, 9159952, 9167820, 9283243, 9383406, 9945758, 9982284, 9983455, 9986419, 10126202, 10156568, 10337935; ZIMB-32-118 9143871, 9391316, 9917748, 9948669, 9982251, 9995331, 10136646, 13011206, 13014574; ZIMB-32-128 9037772, 9159955, 9361554, 9423265, 10156570; ZIMB-32-84 9040645, 9136551, 9159958, 9159959, 9159962, 9167828, 9193807, 9193809, 9239290, 9239292, 9242443, 9301043, 9330500, 9373494, 9391318, 9406725, 9406728, 9917759, 9951141, 9982291, 9986422, 9995339, 10007656, 10007660, 10013759, 10017297, 10017298, 10051126, 10051157, 10062699, 10062781, 10073701, 10077029, 10110453, 10156572, 10288184, 10297335, 10299417, 10307043, 13098184, 13105403; ZIMB-32-98 9060391, 9060393, 9088571, 9132417, 9201608, 9214705, 9217930, 9234937, 9234938, 9234939, 9286012, 9286110, 9307514, 9324523, 9406730, 9406733, 9406735, 9423268, 9936717, 9936719, 9974787, 9986425, 9999375, 10007664, 10013762, 10062785, 10077088, 10113555, 10126227, 10163191, 10163203, 10167625, 10335581, 13010201, 13030131, 13030132, 13030133, 13082901, 13105407; ZIMB-36-108 9130033, 9150330, 9159890, 9365255, 9386647, 9406737, 9406738, 9995345, 9999376, 10139139, 13030135, 13074793, 13082903; ZIMB-36-118 9132489, 9376500, 10129806, 10151121; ZIMB-36-128 9915031, 10090273; ZIMB-36-84 9132418, 9132427, 9132428, 9132496, 9184767, 9303240, 9330504, 9330505, 9406742, 9904232, 9974792, 10077064, 10307049, 13035572; ZIMB-36-98 9132500, 9391321, 9959249, 10110457, 10166133, 10167626, 10297331, 10331476.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2964-2020
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2964-2020	Class II	Terminated	Voluntary: Firm initiated	2020-09-23	2020-09-11

Product code MIH

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)