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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 Guider Softip XF, 40 XF, 8F, Guide Catheter, REF H965100440 2 08/25/2022 Boston Scientific Corporation
Boston Scientific Guider Softip XF Guide Catheter Product Usage: Is a neurovascular access cath... 2 08/08/2018 Boston Scientific Corporation
Guider Softip XF; GUIDER MPXF 5F 100CM, Model number: M003101630. Cardiology: Boston Scientifi... 2 11/02/2016 Stryker Neurovascular
Guider Softip XF; GUIDER 40XF 5F 90CM, Model number:M003100620 . 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/40DEG XF/7FR/90CM, Model number: H965100430 . Cardiology: Boston Scie... 2 11/02/2016 Stryker Neurovascular
Guider Softip XF; GUIDER/MP XF/8FR/100 cm, Model number: M003101480. Cardiology: Boston Scient... 2 11/02/2016 Stryker Neurovascular
Guider Softip XF; GUIDER/MP XF/7FR/90CM, Model number: H965100470. Cardiology: Boston Scientif... 2 11/02/2016 Stryker Neurovascular
Guider Softip XF; GUIDER/MP XF/6FR/90CM, Model number: H965100460. Cardiology: Boston Scientif... 2 11/02/2016 Stryker Neurovascular
Guider Softip XF; GUIDER/ST XF/8FR/90CM, Model number: H965100520. Cardiology: Boston Scientif... 2 11/02/2016 Stryker Neurovascular
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