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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-1686-2011 - DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 1, Sterile, DePuy Orthopaedics. This device is intended to restrict bone cement migration into the distal medullary canal during implantatio... 2 03/17/2011 Depuy Orthopaedics, Inc.
Z-1687-2011 - DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 4, Sterile, DePuy Orthopaedics. This device is intended to restrict bone cement migration into the distal medullary canal during implantatio... 2 03/17/2011 Depuy Orthopaedics, Inc.
Z-1690-2011 - DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 5, Sterile, DePuy Orthopaedics. This device is intended to restrict bone cement migration into the distal medullary canal during implantati... 2 03/17/2011 Depuy Orthopaedics, Inc.
Z-1689-2011 - DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 3, Sterile, DePuy Orthopaedics. This device is intended to restrict bone cement migration into the distal medullary canal during implantati... 2 03/17/2011 Depuy Orthopaedics, Inc.
Z-1688-2011 - DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 5, Sterile, DePuy Orthopaedics. This device is intended to restrict bone cement migration into the distal medullary canal during implantatio... 2 03/17/2011 Depuy Orthopaedics, Inc.
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