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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 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 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 STRAIGHT XF 5F 90CM, Model number: . M003100640. Cardiology: Boston Sc... 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/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
Guider Softip XF; GUIDER/40DEG XF/6FR/90CM, Model number: H965100420. Cardiology: Boston Scien... 2 11/02/2016 Stryker Neurovascular
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