Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System
Reported: September 17, 2025 Initiated: August 6, 2025 #Z-2554-2025
Product Description
Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System
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.
Details
- Recalling Firm
- SEASPINE ORTHOPEDICS CORPORATION
- Units Affected
- 74
- 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.
- Location
- Carlsbad, CA
Frequently Asked Questions
What product was recalled? ▼
Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System. Recalled by SEASPINE ORTHOPEDICS CORPORATION. Units affected: 74.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 17, 2025. Severity: Moderate. Recall number: Z-2554-2025.
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