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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
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Z-1547-05 - Product is an Orthopedic device contained in a Peel Foil Pouch. Product is labeled in part: ''REF C6121 QTY 1 3.5mm Bio-Anchor with Disposable Driver***STERILE***Linvatec A ConMed Company LINVATEC CO... 2 09/21/2005 Linvatec Corp.
Z-1548-05 - Product is an Orthopedic device contained in a Peel Foil Pouch. Product is labeled in part: ''REF C6121H QTY 1 3.5 x 10.5 mm Bio-Anchor with Disposable Driver, Preloaded with One #2 Herculine Suture*... 2 09/21/2005 Linvatec Corp.
Z-1551-05 - Product is an Orthopedic device contained in a Peel Foil Pouch. Product is labeled in part: ''REF***QTY 1 BioScrew XtraLok ***STERILE***Linvatec, LINVATEC CORPORATION LARGO, FL 33773 USA***''. 2 09/21/2005 Linvatec Corp.
Z-1550-05 - Product is an Orthopedic device contained in a Peel Foil Pouch. Product is labeled in part: ''REF*** QTY 1***Hornet Disposable Inserter, BioStinger Implant***STERILE***Linvatec, LINVATEC CORPORATION ... 2 09/21/2005 Linvatec Corp.
Z-1549-05 - Product is an Orthopedic device contained in a Peel Foil Pouch. Product is labeled in part: ''REF C6120A QTY 1 BIO-ANCHOR, PRE-LOADED 3.5mm x 10.5 mm ***STERILE ***Linvatec, LINVATEC CORPORATION LAR... 2 09/21/2005 Linvatec Corp.
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