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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-0843-2013
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NEUROPATH 5Fx90 GUIDING CATH S2 Product Code: GSM50900000 Intended for use in the coronary, peri... 2 02/20/2013 FEI # 3002947440
Codman & Shurtleff, Inc.
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