Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Reef TA Inserter Recalled by SEASPINE ORTHOPEDICS CORPORATION Due to Inserter, used as part of a system with...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact SEASPINE ORTHOPEDICS CORPORATION directly.
Affected Products
Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System
Quantity: 74
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About SEASPINE ORTHOPEDICS CORPORATION
SEASPINE ORTHOPEDICS CORPORATION has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report