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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
Related Medical Device Recalls Recall Date to: 10/13/2015
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Product Description
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FDA Recall
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Z-0150-2013 - SpiraLok 6.5 w/Needles with Orthocord Product Number: 222970 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in ... 2 10/25/2012 DePuy Mitek, Inc., a Johnson & Johnson Co.
Z-0151-2013 - SpiraLok 6.5 w/out Needles with Orthocord Product Number: 222971 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use... 2 10/25/2012 DePuy Mitek, Inc., a Johnson & Johnson Co.
Z-0152-2013 - SpiraLok 5.0 w/Needles with violet and blue Orthocord Product Number: 222985 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indic... 2 10/25/2012 DePuy Mitek, Inc., a Johnson & Johnson Co.
Z-0153-2013 - SpiraLok 5.0 w/out Needles with violet and blue Orthocord Product Number: 222986 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also i... 2 10/25/2012 DePuy Mitek, Inc., a Johnson & Johnson Co.
Z-0154-2013 - SpiraLok 6.5 w/Needles with violet and blue Orthocord Product Number: 222987 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indic... 2 10/25/2012 DePuy Mitek, Inc., a Johnson & Johnson Co.
Z-0141-2013 - SpiraLok 5.0mm with Panacryl and needles Product Number: 222961 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use ... 2 10/25/2012 DePuy Mitek, Inc., a Johnson & Johnson Co.
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