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FDA•Jan 2, 2026MODERATE
ATEC Lateral Navigation Disc Prep Instruments
Alphatec Spine is recalling ATEC Lateral Navigation Disc Prep Instruments due to a design issue with the navigated array connection geometry.
2 products
NHTSA•Jan 2, 2026CRITICAL
Volvo EX30 High-Voltage Battery
Volvo is recalling 2025 EX30 vehicles over high-voltage battery short-circuit and fire risk.
FDA•Jan 2, 2026MODERATE
Lanreotide Injection 120 mg/0.5 mL
Cipla is recalling Lanreotide Injection 120 mg/0.5 mL (NDC 69097-870-67) due to particulate matter contamination.