Every recall we track for EBI, LLC — 4 in all — plus the complaints and injury reports the public filed about them.
Biomet recalls OrthoPak non-invasive bone growth stimulators made since May 2023 due to potential lead wire damage causing treatment delays. Affected units may not deliver therapeutic signals.
EBI recalls 20" lead wires (part 1067724-2) sold since May 2023 due to potential wire damage causing treatment delays. Affected devices may not deliver therapeutic signals properly.
Biomet recalls SpinalPak Non-invasive Spine Fusion Stimulator System (since May 2023) due to potential lead wire damage causing treatment delays. Affected users should contact for remedy.
EBI recalls 48" lead wires (part 1067724-4) sold since May 2023. Damaged sheath may cause treatment delays. Contact for replacement.
