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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 10 Results
510(K) Number: K033639
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Product Description
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Recall
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FDA Recall
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5 Hole Locking 1st Tarsometatarsal Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pass R... 2 09/20/2008 FEI # 1000125930
Acumed LLC
4 Hole Locking 1st Tarsometatarsal Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pass Ro... 2 09/20/2008 FEI # 1000125930
Acumed LLC
4 Hole Locking 2nd and 3rd Tarsometatarsal Plate. Product labeled in part, "ACUMED 5885 NW Corneliu... 2 09/20/2008 FEI # 1000125930
Acumed LLC
Left Locking Proximal Metatarsal Wedge Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pas... 2 09/20/2008 FEI # 1000125930
Acumed LLC
Right Locking 1st MTP/MPJ Combo Fusion Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pas... 2 09/20/2008 FEI # 1000125930
Acumed LLC
Left Locking Dorsal 1st MTP Fusion Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pass Ro... 2 09/20/2008 FEI # 1000125930
Acumed LLC
Left Locking 1st MTP Revision Fusion Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pass ... 2 09/20/2008 FEI # 1000125930
Acumed LLC
Right Locking 1st MTP Revision Fusion Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pass... 2 09/20/2008 FEI # 1000125930
Acumed LLC
Left Locking 2st MTP/MPJ Combo Fusion Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pass... 2 09/20/2008 FEI # 1000125930
Acumed LLC
Right Locking Proximal Metatarsal Wedge Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pa... 2 09/20/2008 FEI # 1000125930
Acumed LLC
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