SEASPINE ORTHOPEDICS Recalls

1 recall found for SEASPINE ORTHOPEDICS. Check if any of your products are affected.

HIGHFDA DEVICE

SEASPINE Orthopedics Recalls Surgical Inserter Over Implant Risks

SEASPINE Orthopedics recalled 74 units of the Reef TA Inserter on August 6, 2025. The device may cause difficulties in disengaging implants, leading to prolonged surgeries. Healthcare providers should stop using the device immediately and follow recall instructions.

SEASPINE ORTHOPEDICS
Inserter, used
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Brand Statistics

Total Recalls
1
Pages
1