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: 788 units Lot/code info: Product Code: 1000211; UDI-DI: 00813502012453; Serial Numbers: 378534 379682 379683 379686 379692 379693 379694 379695 381645 381249 381250 381251 381252 369147 381644 381643 379689 381642 381259 369414 381258 381260 368474 381255 381254 379589 381257 385162 381256 379684 385163 385164 377016A 379690 385157 385158 385181 385166 385167 379591 381248 385168 385169 385174 385183 385170 385177 385535 379696 385540 368769 385666 381641 385667 385555 385644 385645 379588 385557 379685 385558 385538 385552 385178 385559 385620 385553 385554 385643 385641 386021 385171 385668 385619 381262 385671 381261 385672 385673 385674 385669 385537 385675 385688 378530 385184 385689 386037 386036 379691 386025 386126 386039 385536 386130 386136 386128 373298 386133 386134 385539 385175 386135 385159 386043 386058 386142 386060 386143 386144 386145 386147 385686 386149 385616 385670 386137 385551 386131 385542 386127 387494 387513 385617 387492 385543 387514 386023 387490 386150 385176 385541 386132 387521 387522 387520 387510 387497 387496 387509 386063 385544 386141 387515 387516 387517 385173 386064 387519 387529 387500 387501 387503 387524 386148 386022 386065 387511 387502 387824 387530 385556 404252 385642 387822 387823 387495 387534 387508 404249 404268 404248 386038A 387528 385548 387512 406345 386040 405175 405174 387523 405176 405177 405168 405169 405170 387518 404250 405171 406158 405172 404270 387527 406162 385549 387531 385179 385690 385546 387525 386140 385618 405471 405472 405464
00813502012453
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.