Health & Personal Care
HIGH
FDA DEVICE
Cepheid Xpert MTB/RIF GXMTB/RIF-US-10 Recall Affects 9,880 Units in 2025
Cepheid recalled 9,880 units of Xpert MTB/RIF GXMTB/RIF-US-10 after testing failed to meet stability criteria. The devices were distributed nationwide in the United States and Puerto Rico. Health care providers and patients should stop using the device immediately and follow the recall instructions.
Cepheid
Product testing