Cepheid: Medical Device Recalls in 2025
Updated on March 25, 2026.
According to to data from the FDA, there were 4 medical device recalls made by Cepheid in 2025. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10
- Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-10
- Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10.
- Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code: 07332940000158 Xpert SA Nasal Complete kit; 10 test kit: A collection of reagents and other associated materials intended to be used for the direct qualitative and/or quantitative detection of nucleic acid from methicillin-resistant and methicillin-susceptible Staphylococcus aureus (MRSA/MSSA) bacteria present in a clinical specimen, using a nucleic acid technique