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FDA (Device enforcement)Recalled 2021-10-15class ii

Medtronic Vascular, Inc.: Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2820C166EE STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE S

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Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2820C166EE STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE STENT GRAFT ETBF2

  • UPC 00643169781047
  • UPC 00643169781177
  • UPC 00643169780798
  • UPC 00643169780934
  • UPC 00643169780972
  • UPC 00643169781085
  • UPC 00643169781115
  • UPC 00643169781146
  • UPC 00643169781078
  • UPC 00643169232570
  • UPC 00643169780897
  • UPC 00613994991430
  • UPC 00613994991447
  • UPC 00643169232594
  • UPC 00643169780880
  • UPC 00643169780132
  • UPC 00643169781030
  • UPC 00643169780873
  • UPC 00643169780941
  • UPC 00643169781092
  • UPC 00763000099206
  • UPC 00763000099213
  • UPC 00763000099343
  • UPC 00643169366442
  • UPC 00643169781139
  • UPC 00643169215719
  • UPC 00643169780781
  • UPC 00643169781061
  • UPC 00643169781160
  • UPC 00763000099350
  • UPC 00643169780996
  • UPC 00643169781054
  • UPC 00643169781122
  • UPC 00643169780927
  • UPC 00643169780989
  • UPC 00643169781023
  • UPC 00763000099497
  • UPC 00643169215696
  • UPC 00643169781108

Check against the official notice below — it lists the full affected range.

What happened

Medtronic Vascular, Inc. is recalling Endurant II Stent Graft System devices because the spindle may detach from the distal end of the spindle hypotube during stent graft deployment. A total of 511 devices are affected across multiple model numbers, including ETBF2513C145EE, ETBF2820C166EE, ETCF2828C49EE, and ETUF2514C102EE configurations. The devices were distributed worldwide, with U.S. distribution in California, Florida, Georgia, Minnesota, Missouri, North Carolina, New Jersey, New Mexico, Nevada, New York, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, and West Virginia, as well as internationally to Austria, Belgium, Bulgaria, China, Cyprus, Czech Republic, Denmark, Finland, France, Germany, Hungary, Ireland, Italy, Japan, Jordan, Lithuania, Luxembourg, Netherlands, Norway, Poland, Portugal, Qatar, South Africa, Spain, Sweden, and Switzerland.

The recall record does not specify what affected consumers should do regarding these recalled devices.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Due to, during stent graft deployment, the spindle may detach from the distal end of the spindle hypotube.

Details from the source

Reason for recall: Due to, during stent graft deployment, the spindle may detach from the distal end of the spindle hypotube. Distribution: Worldwide distribution - U.S. Nationwide distribution in the states of CA, FL, GA, MN, MO, NC, NJ, NM, NV, NY, PA, SC, TN, TX, VA, and WV. The countries of Austria, Belgium, Bulgaria, China, Cyprus, Czech Republic, Denmark, Finland, France, Germany, Hungary, Ireland, Italy, Japan, Jordan, Lithuania, Luxembourg, Netherlands, Norway, Poland, Portugal, Qatar, South Africa, Spain, Sweden, Switzerland, Quantity: 511 devices Lot/code info: Model Number/GTIN Code/Product Description: ETBF2513C145EE 00643169781047 V30584649 STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593589 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593590 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593591 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593592 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593593 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593594 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593595 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETCF2828C49EE 00643169780798 V30595328 STENT GRAFT ETCF2828C49EE ENDUR II CUFF ETCF2828C49EE 00643169780798 V30595331 STENT GRAFT ETCF2828C49EE ENDUR II CUFF ETCF2828C49EE 00643169780798 V30595332 STENT GRAFT ETCF2828C49EE ENDUR II CUFF ETUF2514C102EE 00643169780934 V30595382 STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE 00643169780934 V30595383 STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE 00643169780934 V30595386 STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE 00643169780934 V30595389 STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE 00643169780934 V30595390 STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE 00643169780934 V30595391 STENT GRAFT ETUF2514C102EE ENDUR II AUI ETBF2313C124EE 00643169780972 V30595456 STENT GRAFT ETBF2313C124EE ENDUR II BIF ETBF2513C145EE 0064

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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