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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-0334-2017
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Guider Softip XF; GUIDER/MP XF/8FR/100 cm, Model number: M003101480. Cardiology: Boston Scient... 2 11/02/2016 FEI # 3008853977
Stryker Neurovascular
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