Medical Device Recalls
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Related Medical Device Recalls |
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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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| Z-1616-2024 - Biomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones, Part Numbe... | 2 | 04/23/2024 |
FEI # 2242816 EBI, LLC |
| Z-1619-2024 - 48" Lead Wires, Replacement Part Number: 1067724-4 | 2 | 04/23/2024 |
FEI # 2242816 EBI, LLC |
| Z-1618-2024 - 20" Lead Wires, Replacement Part Number: 1067724-2 | 2 | 04/23/2024 |
FEI # 2242816 EBI, LLC |
| Z-1617-2024 - Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones. Part Number: ... | 2 | 04/23/2024 |
FEI # 2242816 EBI, LLC |
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