Alphatec recalls specific IdentiTi ALIF graft bolts due to reports of breakage during spinal surgery. Affected units include certain part numbers and lot numbers. Consumers should contact Alphatec for details.
Due to reports of intraoperative graft bolt implantation breakages.
Alphatec is recalling specific IdentiTi ALIF graft bolts that have been reported to break during spinal surgery. This could lead to complications for patients undergoing fusion procedures. Affected units are identified by part numbers and lot numbers.
The graft bolts have been reported to break during spinal surgery, which could cause complications for patients. This breakage may lead to the need for additional surgical interventions or other medical issues.
Patients undergoing spinal fusion procedures using the recalled graft bolts are at risk. Surgeons and medical facilities that have purchased these specific units may also be affected.
Check the product description and part numbers listed in the recall notice. Affected units include specific graft bolts with part numbers like 132-10-85-250 and lot numbers such as 8746709.
Reach out to Alphatec directly to confirm if your specific unit is affected and to get instructions on next steps.
No, these graft bolts are used exclusively in medical spinal fusion procedures by surgeons, not in home or consumer settings.
Check the part number and lot number on your graft bolt against the list provided in the recall notice.
Contact Alphatec directly to determine if your specific unit is affected and to receive instructions on next steps.
We’ve drafted a message you can send Alphatec to request your refund or repair — edit it as you like.
Subject: Recall Z-1182-2024 — Alphatec Alphatec Hello, I own a Alphatec that is covered by recall Z-1182-2024 from Alphatec. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
