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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 Recall Date to: 09/02/2014
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Product Description
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Class
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FDA Recall
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Z-0314-2012 - DePuy Mitek Panalock Loop, Lupine Anchor Catalog #210704 The LUPINE BR Anchor System is indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilizati... 2 11/30/2011 DePuy Mitek, Inc., a Johnson & Johnson Co.
Z-0315-2012 - DePuy Mitek Lupine Loop Plus w/ Orthocord Catalog #210708 The LUPINE BR Anchor System is indicated for use in soft tissue to bone fixation in association with adequate postoperative immobili... 2 11/30/2011 DePuy Mitek, Inc., a Johnson & Johnson Co.
Z-0318-2012 - DePuy Mitek Panalock Loop w/ Orthocord Catalog #222980 The LUPINE BR Anchor System is indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization. 2 11/30/2011 DePuy Mitek, Inc., a Johnson & Johnson Co.
Z-0317-2012 - DePuy Mitek Lupine Loop Rapide w/ Orthocord Catalog #210711 The LUPINE BR Anchor System is indicated for use in soft tissue to bone fixation in association with adequate postoperative immobiliz... 2 11/30/2011 DePuy Mitek, Inc., a Johnson & Johnson Co.
Z-0316-2012 - DePuy Mitek Lupine Loop Plus w/ Orthocord DS Catalog #210709 The LUPINE BR Anchor System is indicated for use in soft tissue to bone fixation in association with adequate postoperative immobi... 2 11/30/2011 DePuy Mitek, Inc., a Johnson & Johnson Co.
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