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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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Guider XF Softip Guide Catheter, manufactured by Boston Scientific Corporation, Maple Grove, MN, dis... 2 11/20/2009 Boston Scientific Corporation
Guider Softip XF; GUIDER/ST XF/8FR/90CM, Model number: H965100520. Cardiology: Boston Scientif... 2 11/02/2016 Stryker Neurovascular
Guider Softip XF; GUIDER/ST XF/6FR/100 cm, Model number:M003101500 . Cardiology: Boston Scient... 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/40XF/8FR/90CM, Model number: H965100440 . Cardiology: Boston Scientif... 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/40DEG XF/6FR/90CM, Model number: H965100420. Cardiology: Boston Scien... 2 11/02/2016 Stryker Neurovascular
Guider Softip XF; GUIDER/40 DEG XF/7FR/100 cm, Model number: M003101430 . Cardiology: Boston S... 2 11/02/2016 Stryker Neurovascular
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