FDA recall record

Becton Dickinson & Co BD GeneOhm Cdiff Assay , Catalog #441400 200, box tests 1-3 labeled in recall — FDA Z-2318-2012

Leakage in Cepheid SmartCycler reaction tubes.

Class IIclassification
Z-2318-2012official record ID
Sep 12, 2012report date

Recall record at a glance

Official recordZ-2318-2012
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBecton Dickinson & Co.
Report dateSep 12, 2012
Recall initiation dateMay 22, 2012
Quantity57 kits
LocationSparks, MD, United States

Official product description

BD GeneOhm Cdiff Assay , Catalog #441400 200, box tests 1-3 labeled in part***BD Diagnostics, 2555 boul, du Parc-Technologique, Quebec, QC, Canada G1P 4S5*** BD GeneOhm Cdiff Assay is a qualitative in vitro diagnostic test for the direct detection of C. difficile toxin gene (tcdB) in human liquid or soft stool specimens fr.om patients suspected of having Clostridium difficile-associated disease (CDAD). The test, based on real-time PCR, is intended for use as an aid in diagnosis of CDAD. The test is performed directly on the specimen, utilizing polymerase chain reaction (PCR) for the amplification of specific targets and fluorogenic target-specific hybridization probes for the detection of the amplified DNA.

Why the product was recalled

Leakage in Cepheid SmartCycler reaction tubes.

Distribution information

Nationwide Distribution including CA, DE, FL, GA, IL, IN, KS, KY, ME, MT, NC, NJ, NM, NY, OH, OK, PA, SC, TX, VA, WA, WI, and WV.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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