⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Is Cepheid recalled?

Cepheid recalls - full list & free alerts

Official U.S. agency records list 4 recalls involving Cepheid in the last 12 months, most recently on 2025-12-24. Check each official notice for the exact products, lot codes and dates affected.

Check a lot code, UPC or model number

This is not a guarantee; check the official notice.

Recalls (4)

Cepheid: Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10
Medical DevicesFDA (device) · 2025-12-24 · Class II
Cepheid: Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-10
Medical DevicesFDA (device) · 2025-12-24 · Class II
Cepheid: Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10.
Medical DevicesFDA (device) · 2025-12-03 · Class II
Cepheid: Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code: 07332940000158 Xpert SA Nasal Complete kit; 10 test kit: A collection
Medical DevicesFDA (device) · 2025-11-05 · Class II
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