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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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Product Description
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FDA Recall
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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-0344-2017 - Guider Softip XF; GUIDER MPXF 5F 90CM, Model number: M003100630. Cardiology: Boston Scientific Guider Softip XF Guide Catheters are intended to facilitate the placement of interventional device... 2 11/02/2016 Stryker Neurovascular
Z-0345-2017 - Guider Softip XF; GUIDER STRAIGHT XF 5F 90CM, Model number: . M003100640. Cardiology: Boston Scientific Guider Softip XF Guide Catheters are intended to facilitate the placement of interventiona... 2 11/02/2016 Stryker Neurovascular
Z-0346-2017 - Guider Softip XF; GUIDER STRAIGHT XF 5F 100CM, Model number: M003101640. Cardiology: Boston Scientific Guider Softip XF Guide Catheters are intended to facilitate the placement of interventional ... 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
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