Devices

Device Recall Xpert MRSA

Model / Serial
Catalog number: GXMRSA-120, Rev. AJ; Lot numbers: 1000037539 (Cartridge lot 20417) and 1000029307 (Cartridge lot 20419).
Product Classification
Immunology and Microbiology Devices
Device Class
2
Implanted device?
No
Distribution
US only: PA, DE, FL, SC, ME, CA, IL, NC, TX, WA, NY, TN, FL, OR, OK, MO, MS, GA, NM, IN, OH, MD, VA, CO, AZ, and NC.
Product Description
Xpert MRSA || Catalog GXMRSA-120, Rev. AJ || Microbiology: || The Cepheid Xpert MRSA assay performed in the GeneXpert Dx System || (Xpert MRSA) is a qualitative in vitro diagnostic test designed for rapid detection of Methicillin-Resistant Staphylococcus Aureus (MRSA) from nasal swabs in patients at risk for nasal colonization
Manufacturer
Cepheid
1 Event
- Recall of Device Recall Xpert MRSA

Manufacturer

Cepheid

Manufacturer Address
Cepheid, 904 E Caribbean Dr, Sunnyvale CA 94089-1189
Manufacturer Parent Company (2017)
Danaher Corporation
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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