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FDA (Device enforcement)Recalled 2025-08-06class ii

SEASPINE ORTHOPEDICS CORPORATION: Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System

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.

Details from the source

Reason for recall: 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. Distribution: 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. Quantity: 74 Lot/code info: UDI-DI: 10889981290733, 10889981437800. Lots: BT107376C, BT112289C, BT112779C, BT107376CR1, BT107376CR2, BT107376CR1R2, BT112289CR2, BT112779CR2

UPC codes

10889981290733, 10889981437800

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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