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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 20 Results
510(K) Number: K980453
 
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Product Description
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FDA Recall
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Boston Scientific 6F Guider Softip XF Guiding Catheter, 6 French, 40 degree angle, 100cm usable len... 3 11/24/2007 Boston Scientific Target
Boston Scientific 6F Guider Softip XF Guiding Catheter, 6 French, 40 degree angle, 90cm usable lengt... 3 11/24/2007 Boston Scientific Target
Boston Scientific Guider Softip XF Guide Catheter Product Usage: Is a neurovascular access cath... 2 08/08/2018 Boston Scientific Corporation
Boston Scientific Guider Softip XF, 40 XF, 8F, Guide Catheter, REF H965100440 2 08/25/2022 Boston Scientific Corporation
Guider Softip XF; GUIDER 40XF 5F 90CM, Model number:M003100620 . Cardiology: Boston Scientific... 2 11/02/2016 Stryker Neurovascular
Guider Softip XF; GUIDER MPXF 5F 100CM, Model number: M003101630. Cardiology: Boston Scientifi... 2 11/02/2016 Stryker Neurovascular
Guider Softip XF; GUIDER MPXF 5F 90CM, Model number: M003100630. Cardiology: Boston Scientific... 2 11/02/2016 Stryker Neurovascular
Guider Softip XF; GUIDER STRAIGHT XF 5F 100CM, Model number: M003101640. Cardiology: Boston Scie... 2 11/02/2016 Stryker Neurovascular
Guider Softip XF; GUIDER STRAIGHT XF 5F 90CM, Model number: . M003100640. Cardiology: Boston Sc... 2 11/02/2016 Stryker Neurovascular
Guider Softip XF; GUIDER/40 DEG XF/6FR/100 cm, Model number: M003101420. Cardiology: Boston Sc... 2 11/02/2016 Stryker Neurovascular
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