Xpert MTB/RIF
CEPHEID · Model GXMTB/RIF-US-10 · UDI-DI 07332940000912
PEU
Prescription
2
510(k) clearances
3
Adverse events
1
Recalls
3
Facilities
Description
Xpert MTB/RIF kit; 10 test kit
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-11-05 | Cepheid | Product testing did not meet expected stability criteria. |
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.