Home / Recalls / Medical Devices
SEASPINE ORTHOPEDICS CORPORATION recalls Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System
Recalled September 17, 2025 · FDA recall Z-2554-2025 · SEASPINE ORTHOPEDICS
Hazard
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. · FDA Class II
Units
74
Sold at
Worldwide - US Nationwide distribution in the states of NV, TX, ID, MI, OH, SD, TN, PA, CT, CO, FL, WA, NC, OK, MN and the country of Hong Kong.
Description
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.
Product
Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System
Manufacturer(s)
SEASPINE ORTHOPEDICS CORPORATION
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →