A potential device interaction between the Shockwave Coronary IVL Catheter and left-sided Impella Pumps during coronary interventions. Currently there is no Abiomed labeling (IFU etc.) content related to this potential interaction, so Abiomed will update the IFU to include information on this potential device interaction.
Reason for recall: A potential device interaction between the Shockwave Coronary IVL Catheter and left-sided Impella Pumps during coronary interventions. Currently there is no Abiomed labeling (IFU etc.) content related to this potential interaction, so Abiomed will update the IFU to include information on this potential device interaction. Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Brazil, Brunei Darussalam, Canada, Croatia, Czeck Republic, Denmark, Finland, France, Germany, Hong Kong, India, Ireland, Israel, Italy, Japan, Kuwait, Luxembourg, Malaysia, Mexico, Netherlands, Norway, Panama, Poland, Saudi Arabia, Serbia, Singapore, Slovenia, Spain, Sweden, Switzerland, Taiwan, U.A.E., Unite Quantity: 11,236 units Lot/code info: Product Code: 1000080; UDI-DI: 00813502012279; Serial Numbers: 411717 411718 411715 411716 411720 411721 411722 411723 411724 411705 411706 411707 411711 411712 411719 411814 411813 411812 411811 411810 411809 411708 411709 411710 411713 411714 411808 411807 411806 411805 411866 411867 412111 412112 412142 412143 412110 412113 412114 412115 412116 412117 412141 412000 412148 412146 412144 412145 412140 412147 412001 412003 411860 411861 411862 411863 411864 412004 412005 411321 411477 411473 411474 411310 411890 411889 411888 411887 411475 411476 411468 411467 411469 411470 411301 411478 411461 411462 411463 411464 411465 411472 411303 411304 411309 411466 411302 411305 411306 411307 411892 411893 411894 411895 411896 412461 412463 412465 412301 412330 412331 412332 412333 412334 412335 412336 412337 412338 411891 412467 412149 412299 412300 412303 412304 412305 412308 412329 412459 412458 412460 412462 412464 412306 412307 411546 411547 411549 411550 411733 411855 412888 412889 412890 412891 411541 411542 412309 411730 411731 411732 411734 411851 411853 412892 412893 411543 411544 411856 411857 411858 412887 411859 412884 412885 413323 413324 413325 413326 412918 412917 412916 412914 413321 413322 412317 412318 413327 413328 412312 412316 412638 412639 412640 412642 413329 413330 412313 412314 412633 412634 412635 412636 412310 412311 413965 413966 413967 413968 413969 413970 412270 412027 412028 414267 414269 414270 414271 414272 414273 413526 413527 413528 413529 413971 41
00813502012279
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.