Alphatec Spine Recalls

2 recalls found for Alphatec Spine. Check if any of your products are affected.

HIGHFDA DEVICE

Jan 2, 2026

Alphatec Spine Recalls Lateral Navigation Disc Prep Instruments Due to Design Flaw

Alphatec Spine recalled 15 units of Lateral Navigation Disc Prep Instruments on January 2, 2026, due to a design flaw. The navigated array connection geometry is incorrect, posing risks during surgical procedures. Healthcare providers and patients should stop using the instruments immediately.

Alphatec Spine

Due a

HIGHFDA DEVICE

Jan 2, 2026

Alphatec Spine Recalls Surgical Instruments Over Connection Issue

Alphatec Spine recalled 7 units of Lateral Navigation Disc Prep Instruments on January 2, 2026, due to a design flaw. The incorrect navigated array connection geometry poses a high hazard risk in surgical settings. Healthcare providers and patients must stop using the devices immediately.

Alphatec Spine

Due a

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Total Recalls

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