SEASPINE recalls Reef TA Inserter (Part TA2-001003) due to potential improper implant positioning during spinal surgery. Affected units have specific UDI-DI markings and lot numbers.
Inserter, used as part of a system with an intervertebral body fusion device, may contribute to difficulty disengaging the implant or improper implant positioning, which may may lead to prolonged surgery, intraoperative revision, and may require the use of alternate instrumentation. Devices may also have incorrect UDI-DI marking.
SEASPINE is recalling Reef TA Inserter parts (model TA2-001003) because they may cause improper spinal implant positioning, leading to longer surgeries or revisions. This affects surgeons using the Reef Interbody System.
The inserter may not disengage properly from the implant, causing misalignment during spinal fusion surgery. This could lead to longer procedures, additional surgeries, or the need for different tools.
Surgeons and medical facilities using the Reef Interbody System with the specific part number TA2-001003 are most at risk. The recall applies to devices sold with certain UDI-DI markings and lot numbers.
Check for UDI-DI markings: 10889981290733 or 10889981437800. Also look for lot numbers: BT107376C, BT112289C, BT112779C, or similar variants.
Look for UDI-DI numbers 10889981290733 or 10889981437800 on the device.
Confirm the lot numbers match BT107376C, BT112289C, BT112779C, or similar variants.
The Reef TA Inserter may cause improper implant positioning during spinal fusion surgery, leading to longer procedures or revisions.
Check the UDI-DI markings and lot numbers to confirm if your device is affected. If it is, contact SEASPINE for guidance.
The recall addresses potential surgical complications, but the official notice does not specify a risk of serious injury in normal use.
We’ve drafted a message you can send SEASPINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2554-2025 — SEASPINE SEASPINE Hello, I own a SEASPINE that is covered by recall Z-2554-2025 from SEASPINE. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
