Z-0153-2020 Class III Terminated

Recalled by Roche Diagnostics Operations, Inc. — Indianapolis, IN

Recall Details

Product Type
Devices
Report Date
October 23, 2019
Initiation Date
September 11, 2019
Termination Date
June 11, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
2,304 units

Product Description

Cobas c Bilirubin Total Gen.3 Catalog Number: 05795419190 - Product Usage: In vitro test for the quantitative determination of the total bilirubin in serum and plasma of adults and neonates on Roche/Hitachi cobas c systems.

Reason for Recall

Due to low Quality Control recovery and invalid Calibration.

Distribution Pattern

US Nationwide distribution including the states of AL, AZ, CA, CT, FL, GA, HI, IA, IL, IN, KY, LA, MA, MD, MI, MO, NE, NH, NJ, NY, OH, OK, PA, PR, RI, SC, TN, TX, UT, VA and WI. Updated as of 12/20/19 to include the following additional US states: CO.

Code Information

Lot # 36133801