Every recall we track for Cepheid — 9 in all — plus the complaints and injury reports the public filed about them.
Cepheid recalls Xpert MTB/RIF model GXMTB/RIF-US-10 due to instability in product testing. Affected units may not meet stability criteria. Contact for remedy details.
Cepheid recalls Xpert BCR-ABL Ultra test kits with elevated white blood cell counts that may cause inaccurate results. Affected kits have specific model and lot numbers.
Cepheid recalls Xpert BCR-ABL Ultra test kits with elevated white blood cell counts that may cause inaccurate results. Affected kits have specific model numbers and lot numbers.
Cepheid recalls Xpert SA Nasal Complete kits with catalog number GXSACOMP-10 and UDI-DI code 07332940000158 due to false negative results in post-market testing. Affected kits may not detect MRSA/MSSA bacteria correctly.
Cepheid recalls sample collection device part 900-0370 due to potential leaks after swab insertion, risking biohazard exposure and false test results. Affected units have specific lot numbers and expiration dates.
Cepheid recalls Xpert Xpress Strep A tests with specific lot numbers due to potential for invalid results from improper sample volume dispensing.
Cepheid recalls Xpert Xpress Strep A tests with potential for invalid results due to pipette issues. Affected units include specific lot numbers and model.
