Affinity Fusion" Oxygenator with Integrated Arterial Filter, Affinity Fusion cardiotomy/Venous Reservoir, Perfusion Tubing Packs The Affinity Fusion Oxygenator with Integrated Arterial Filter with or without the Cardiotomy/Venous Reservoir with Balance¿1 Biosurface is intended for use in an extracor
Check against the official notice below — it lists the full affected range.
Medtronic is voluntarily recalling specific lot numbers of Affinity Fusion Oxygenators with Balance Biosurface, which may be sold as standalone devices, combined with Affinity Fusion Cardiotomy/Venous Reservoirs, or as part of perfusion tubing packs. The recall affects approximately 5,609 units (663 in the U.S. and 4,946 outside the U.S.) distributed across multiple states and countries including the United States, Canada, Chile, Croatia, Germany, Greece, Hungary, Iran, Italy, Latvia, Lebanon, Poland, Portugal, Romania, Spain, Tanzania, and the United Kingdom. The products are being recalled because an out-of-specification condition has been identified: additional plastic material (flash) was found in the arterial sampling port adjacent to the arterial outlet port of the oxygenator.
The affected lot numbers are listed in a detailed table provided in the recall documentation with specific product UPN/GTIN codes. Consumers who may have received one of these products should check the lot and product numbers against the provided list. The recall documentation does not specify what actions affected consumers should take in response to this recall.
Written by software from the official notice below. Not reviewed by a lawyer.
Medtronic is initiating a voluntary product recall for specific lot numbers of the Affinity Fusion¿ Oxygenators with Balance¿1 Biosurface. These are distributed as stand-alone devices, or as a combination unit with the Affinity Fusion Cardiotomy/Venous Reservoir, or as part of tubing packs. Medtronic has identified an out-of-specification condition exhibiting additional plastic (flash) in the arterial sampling port adjacent to the arterial outlet port of the oxygenator.
Reason for recall: Medtronic is initiating a voluntary product recall for specific lot numbers of the Affinity Fusion¿ Oxygenators with Balance¿1 Biosurface. These are distributed as stand-alone devices, or as a combination unit with the Affinity Fusion Cardiotomy/Venous Reservoir, or as part of tubing packs. Medtronic has identified an out-of-specification condition exhibiting additional plastic (flash) in the arterial sampling port adjacent to the arterial outlet port of the oxygenator. Distribution: Worldwide Distribution-US (nationwide) in states of: AK, AZ, CA, CO, CT, FL, IA, IL, IN, KS, KY, LA, MN, ND, NV, NY, SD, TN, TX, WI, WY and countries of: Canada, Chile, Croatia, Germany, Greece, Hungary, Iran, Italy, Latvia, Lebanon, Poland, Portugal, Romania, Spain, Tanzania, and United Kingdom. Quantity: 5609 (663 US; 4946 OUS) Lot/code info: Product UPN/GTIN Lot Number Product Number 00643169650749 212028376 HY8N22R8 00643169802421 211984809 BB9D23R3 00643169707801 211991294 BB1D41R27 00643169871908 212073806 HY8B75R12 00643169621473 211950617 BB8U95R1 00643169860322 211865249 BB8E47R15 00643169865365 211975385 BB9D32R2 00643169860322 211991184 BB8E47R15 00643169717336 211991250 BB8Q09R2 00643169792852 211991385 BB9G59R5 00643169740020 211991295 HY8C67R10 00643169649101 211991248 BB7H73R14 00643169868120 212028234 BB8G43R3 00643169860322 212028305 BB8E47R15 00643169873032 212034498 HY9L88R2 00643169534629 212109150 BB7Z44R6 00643169591738 211846477 BB1A19R44 00643169786790 211991196 BB8X02R7 00643169639058 211846421 BB8N94R4 00643169649767 211991286 HY8J73R6 00643169869783 211991482 BB9E16R4 00643169861534 211914227 SSHY9M26R 00643169869516 211974259 BB9L66R 00643169872127 212020797 BB9L72R1 00643169736283 212028295 BB8S37R11 00643169776807 212028317 BB7X32R12 00643169546431 212028362 BB8C09R4 00643169786042 212028304 BB8Y15R1 00643169471597 212028389 BB4W65R13 00643169793699 212073805 BB8C33R6 00643169792036 211846376 BB8N34R5 00643169631649 212021402 BB8T05R1 00643169587106 212073934 HY0W84R28 00643169862920 211991252 HY8H59R17 00643169845121 212073924 BB4B15R13 00643169648111 211885327 BB8A57R11 00643169741720 211804528 BB3M00R29 00643169700284 211807907 HY1F66R18 00643169766839 211957793 BB8D44R4 00643169518131 211957865 HY8B26R4 00643169463929 211885289 BB5Z97R14 00643169714229 211991298 BB7U21R17 0064316961
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.