Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-1303-2019 - T7 Driver Solid AO (Part Number 110018541) Product Usage: The Biomet Headless Compression Screws and Twist-Off Screws are indicated for fixation of bone fractures, fusion of a joint (arthrodesis) ... | 2 | 05/09/2019 |
FEI # 1825034 Zimmer Biomet, Inc. |
| Z-1302-2019 - T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Biomet Headless Compression Screws and Twist-Off Screws are indicated for fixation of bone fractures, fusion of a joint (arthrode... | 2 | 05/09/2019 |
FEI # 1825034 Zimmer Biomet, Inc. |
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