EBI, LLC: Medical Device Recalls in 2024

According to to data from the FDA, there were 4 medical device recalls made by EBI, LLC in 2024. See the details of the recalls below.

You can see similar recalls for other firms.

• 20" Lead Wires, Replacement Part Number: 1067724-2
• 48" Lead Wires, Replacement Part Number: 1067724-4
• 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 Number: 1067716
• 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: 1067718