Every recall we track for Abbott Vascular — 29 in all — plus the complaints and injury reports the public filed about them.
Abbott Vascular recalls MitraClip G4 CDS and TriClip devices due to potential clip locking malfunctions that could lead to severe heart valve issues during cardiac procedures.
Abbott Vascular recalls MitraClip NTR and other clip delivery systems due to increased risk of clip locking malfunctions during cardiac procedures, which may cause severe mitral regurgitation or device embolization.
Abbott Vascular recalls MitraClip XTR and G4 Clip Delivery Systems due to increased clip locking malfunctions that could cause severe heart problems during cardiac procedures.
Abbott Vascular recalls Dragonfly OpStar Imaging Catheters with potential for proximal marker separation. Affected models include REF 1014651/1014652, 0.068 in, 0.014 in, 135 cm, STERILE EO. Contact Abbott for details.
Abbott Vascular recalls 20/30 Priority Pack w/COPILOT devices from 2019 with leaks and intermittent connections. Affected units include specific lot numbers and part numbers.
Abbott Vascular recalls 20/30 Priority Pack Accessory Kits with potential leaks and loose connections. Affected units include specific part numbers and lot numbers from 2019. Contact for remedy details.
Abbott Vascular recalls 20/30 INDEFLATORS with specific part numbers due to reported leaks and intermittent connections. Owners should check their device identifiers and lot numbers for affected units.
Abbott Vascular recalls INDEFLATOR Plus 30 devices with leaks or loose connections. Affected units have specific part numbers and lot numbers from March 2019.
Abbott Vascular recalls Plus 30 Priority Packs with .096 and .115 RHV models due to reported leaks and intermittent connections. Affected units include specific part numbers and lot numbers.
Abbott recalls Xience Sierra Everolimus stents with incorrect expiration dates. Affected stents may be unsafe for use. Contact Abbott for details.
Abbott recalls NC TREK Coronary Dilatation Catheters (REF 1012453-15) due to potential balloon deflation issues. This may affect medical procedures requiring coronary artery dilation.
Abbott Vascular recalls NC TREK Coronary Dilatation Catheters that may have difficulty deflating the balloon, potentially causing complications during procedures.
Abbott Vascular recalls NC TREK Coronary Dilatation Catheters (REF 1012455-12) due to potential balloon deflation issues. Affected units may cause complications during medical procedures.
Abbott recalls NC Traveler Coronary Dilatation Catheters (REF 10131:12) due to potential balloon deflation issues. This device is not cleared for US distribution.
Abbott Vascular recalls NC TREK Coronary Dilatation Catheters (REF 1012453-08) due to potential balloon deflation issues. Affected units include specific lot numbers sold for medical use only.
Abbott Vascular recalls NC TREK Coronary Dilatation Catheters that may have difficulty deflating the balloon, which could cause injury during procedures. Affected units include specific model and lot numbers.
Abbott Vascular recalls NC Traveler Coronary Dilatation Catheters (REF 1013157-08) due to potential balloon deflation issues. This device is not cleared for U.S. distribution.
Abbott Vascular recalls NC TREK Coronary Dilatation Catheters (REF 1012454-20) due to potential balloon deflation issues. This may affect medical procedures requiring coronary artery dilation.
Abbott Vascular recalls NC TREK Coronary Dilatation Catheters (REF 1012453-12) due to potential balloon deflation issues. Affected units include specific lot numbers and sizes.
Abbott Vascular recalls NC TREK Coronary Dilatation Catheters (REF 1012454-15) due to potential balloon deflation issues. This may affect medical procedures requiring coronary artery dilation.
Abbott Vascular recalls NC TREK Coronary Dilatation Catheters with potential balloon deflation issues. Affected units have specific lot numbers and part numbers. Consumers should contact Abbott for details.
Abbott Vascular recalls NC TREK Coronary Dilatation Catheters that may have difficulty deflating the balloon, potentially causing blockages during procedures. Affected models include REF 1012455-08 Rx Only, NC TREK RX 5.00 X 8MM BDC.
Abbott recalls NC Traveler Coronary Dilatation Catheters (REF 1013157-12) due to potential balloon deflation failure. This device is not cleared for U.S. distribution and may cause complications during procedures.
Abbott Vascular recalls NC Traveler Coronary Dilatation Catheters (REF 1013158-08) due to potential balloon deflation failure. This may cause complications during procedures. Affected units were sold with specific lot numbers.
Abbott recalls NC TREK Coronary Dilatation Catheters with potential balloon deflation issues. This device is used for coronary artery procedures and may cause complications if the balloon cannot deflate properly.
Abbott Vascular recalls NC TREK Coronary Dilatation Catheters that may have difficulty deflating the balloon, which could lead to complications during medical procedures.
Abbott recalls NC Traveler Coronary Dilatation Catheters (REF 1013157-15) due to potential balloon deflation issues. This device is not cleared for U.S. distribution and may cause complications during procedures.
Abbott recalls MitraClip XTR Clip Delivery System due to risk of clips opening unexpectedly during implantation, potentially requiring additional surgery. Affected units have specific serial numbers.
Abbott Vascular recalls PLUS : 30 PRIORITY PACK Accessory Kit due to potential incorrect expiration entry for one lot. This may affect medical device safety during vascular procedures.
