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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 14 Results
510(K) Number: K112885
 
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Product Description
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Recall
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FDA Recall
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PERI SCR. 3.5MM X 10MM PERI SCR. 3.5MM X 12MM PERI SCR. 3.5MM X 14MM PERI SCR 3.5MM X 44... 2 02/20/2014 FEI # 1000220733
Zimmer, Inc.
Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile zimmer 2 08/16/2014 FEI # 1000220733
Zimmer, Inc.
4.5 mm Malleolar Screw Sterile zimmer 2 08/16/2014 FEI # 1000220733
Zimmer, Inc.
6.5 mm Cancellous Screw Fully Threaded Sterile zimmer 2 08/16/2014 FEI # 1000220733
Zimmer, Inc.
6.5 mm Cancellous Screw 32 mm Thread Length Sterile zimmer 2 08/16/2014 FEI # 1000220733
Zimmer, Inc.
6.5 mm Cancellous Screw 16 mm Thread Length Sterile zimmer 2 08/16/2014 FEI # 1000220733
Zimmer, Inc.
4.0 mm Cancellous Screw, Partially Threaded Sterile Zimmer 2 08/16/2014 FEI # 1000220733
Zimmer, Inc.
Magna-Fx Cannulated Screw Fixation System Cannulated Bone Screw Sterile zimmer 2 08/16/2014 FEI # 1000220733
Zimmer, Inc.
6.5 mm Cancellous Screw Fully Threaded Sterile zimmer 2 08/16/2014 FEI # 1000220733
Zimmer, Inc.
Product 4 consists of all products under product code HWC, and same usage: Item no: 47482002603 ... 2 03/12/2016 FEI # 1000132037
Zimmer Manufacturing B.V.
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