SPINEART recalls specific JULIET Ti Lateral Lumbar Ti-Life Plate models that may disassemble during surgery, causing delays. Affected patients should contact SPINEART for guidance.
JULIET Lateral Lumbar Ti-Life Plate, a component of the JULIET Ti Lateral Lumbar Cage, may disassemble during the preparation stage before implantation, or during surgery when removing the implant holder, which could cause surgical delay.
SPINEART is recalling certain JULIET Ti Lateral Lumbar Ti-Life Plate models that may disassemble during surgery or implant removal, potentially causing delays. This is a critical issue for patients undergoing spinal surgery.
The plate may disassemble during the preparation stage before implantation or when removing the implant holder during surgery. This disassembly can cause surgical delays, which may impact recovery and treatment outcomes.
Patients who have received the recalled JULIET Ti Lateral Lumbar Ti-Life Plate models for spinal surgery are most at risk. These items were used in specific surgical procedures.
Check for model numbers JLT-PL 02 08-S, 02 10-S, 02 12-S, 02 14-S, 02 16-S, 04 08-S, 04 10-S, 04 12-S, 04 14-S, or 04 16-S, 04 18-S. The recall includes specific lot numbers and reference codes listed in the official notice.
Reach out to SPINEART directly for guidance on next steps and potential remedies for affected patients.
The JULIET Lateral Lumbar Ti-Life Plate may disassemble during surgery or implant removal, causing delays.
Models JLT-PL 02 08-S, 02 10-S, 02 12-S, 02 14-S, 02 16-S, 04 08-S, 04 10-S, 04 12-S, 04 14-S, and 04 16-S, 04 18-S are affected.
No immediate stop is required, but affected patients should contact SPINEART for guidance on next steps.
We’ve drafted a message you can send SPINEART to request your refund or repair — edit it as you like.
Subject: Recall Z-1426-2023 — SPINEART SPINEART Hello, I own a SPINEART that is covered by recall Z-1426-2023 from SPINEART. 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.
