Health & Personal Care
HIGH
FDA DEVICE
Cepheid Recalls Xpert MTB/RIF Test Due to Stability Issues
Cepheid recalled 9,880 units of the Xpert MTB/RIF testing device on November 5, 2025. Product testing failed to meet expected stability criteria, leading to potential inaccuracies. Healthcare providers and patients must stop using the device immediately.
Cepheid
Product testing