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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 16 of 16 Results
510(K) Number: K060271
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Product Description
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Recall
Class
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FDA Recall
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SpiraLok 6.5 w/Needles with Orthocord Product Number: 222970 SPIRALOK Anchors are primarily used... 2 10/25/2012 DePuy Mitek, Inc., a Johnson & Johnson Co.
SpiraLok 6.5 w/out Needles with Orthocord Product Number: 222971 SPIRALOK Anchors are primarily ... 2 10/25/2012 DePuy Mitek, Inc., a Johnson & Johnson Co.
SpiraLok 5.0 w/Needles with violet and blue Orthocord Product Number: 222985 SPIRALOK Anchors ar... 2 10/25/2012 DePuy Mitek, Inc., a Johnson & Johnson Co.
SpiraLok 5.0 w/out Needles with violet and blue Orthocord Product Number: 222986 SPIRALOK Anchor... 2 10/25/2012 DePuy Mitek, Inc., a Johnson & Johnson Co.
SpiraLok 6.5 w/Needles with violet and blue Orthocord Product Number: 222987 SPIRALOK Anchors ar... 2 10/25/2012 DePuy Mitek, Inc., a Johnson & Johnson Co.
SpiraLok 5.0mm with Panacryl and needles Product Number: 222961 SPIRALOK Anchors are primarily u... 2 10/25/2012 DePuy Mitek, Inc., a Johnson & Johnson Co.
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