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Lsi Medience Recalls

1 recall on record · November 30, 2016 to November 30, 2016 · Medical Devices

November 30, 2016Medical DevicesFDA

Lsi Medience Corporation recalls Pathfast D-Dimer, Reference number: PF1051-KUS

Hazard: Two complaints were received about decrease in sensitivity (control value and/or calibration value) of the product.

Lsi Medience Recalls | RecallWatchUSA