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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 7 of 7 Results
510(K) Number: K021932
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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6.5 mm Cannulated Screw, Product code HWC, Device Listing Number D028949, Screw, Fixation Bone Pr... 2 07/11/2016 Synthes (USA) Products LLC
6.5 mm Cancellous Screw, Product code HWC, Device Listing Number D029043, Screw, Fixation Bone Pr... 2 07/11/2016 Synthes (USA) Products LLC
7.0 mm and 7.3 mm Cannulated Screw, Product code HWC, Device Listing Number D068620, Plate, Fixation... 2 07/11/2016 Synthes (USA) Products LLC
3.5 mm and 4.0 mm Cannulated Screw, Product code HWC, Device Listing Number D029094, Screw, Fixation... 2 07/11/2016 Synthes (USA) Products LLC
4.5 mm Cortex Screw, Product code HWC, Device Listing Number D137402, Screw, Fixation Bone Produc... 2 07/11/2016 Synthes (USA) Products LLC
4.5 mm Cannulated Screw, Product code HWC, Device Listing Number D029092 and D120718, Screw, Fixatio... 2 07/11/2016 Synthes (USA) Products LLC
4.0 mm Cortex Screw, Product code HWC, Device Listing Number D137404 and D137402, Screw, Fixation Bo... 2 07/11/2016 Synthes (USA) Products LLC
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