Official recall record
Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2025-08-06
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 10889981290733
- Brand on record
- SEASPINE ORTHOPEDICS CORPORATION
- Product category
- Medical Device
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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