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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.
See this for other years:
2015
2016
2017
2018
2023
2024
2025
  • 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
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