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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 15 of 15 Results
Related Medical Device Recalls
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FDA Recall
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Z-0336-2017 - Guider Softip XF; GUIDER/MP XF/6FR/90CM, Model number: H965100460. Cardiology: Boston Scientific Guider Softip XF Guide Catheters are intended to facilitate the placement of interventional devi... 2 11/02/2016 Stryker Neurovascular
Z-0335-2017 - Guider Softip XF; GUIDER/MP XF/7FR/90CM, Model number: H965100470. Cardiology: Boston Scientific Guider Softip XF Guide Catheters are intended to facilitate the placement of interventional devi... 2 11/02/2016 Stryker Neurovascular
Z-0334-2017 - Guider Softip XF; GUIDER/MP XF/8FR/100 cm, Model number: M003101480. Cardiology: Boston Scientific Guider Softip XF Guide Catheters are intended to facilitate the placement of interventional de... 2 11/02/2016 Stryker Neurovascular
Z-0343-2017 - Guider Softip XF; GUIDER/ST XF/6FR/100 cm, Model number:M003101500 . Cardiology: Boston Scientific Guider Softip XF Guide Catheters are intended to facilitate the placement of interventional de... 2 11/02/2016 Stryker Neurovascular
Z-0337-2017 - Guider Softip XF; GUIDER/ST XF/8FR/90CM, Model number: H965100520. Cardiology: Boston Scientific Guider Softip XF Guide Catheters are intended to facilitate the placement of interventional devi... 2 11/02/2016 Stryker Neurovascular
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