PlainRecalls
FDA Devices Moderate Class II Terminated

Cobas c8000 Modular Analyzer Series Cobas c502, Part Number 5964067001, a clinical chemistry analyzer intended for the in vitro quantitative / qualitative determination of analytes in body fluids.

Reported: April 16, 2014 Initiated: March 13, 2014 #Z-1449-2014

Product Description

Cobas c8000 Modular Analyzer Series Cobas c502, Part Number 5964067001, a clinical chemistry analyzer intended for the in vitro quantitative / qualitative determination of analytes in body fluids.

Reason for Recall

The Initial Cassette Volume Check (ICVC) is not activated on the cobas c 502 module of the cobas 8000 modular analyzer series when manually filled cobas c packs are loaded. This issue occurs with tests that use cobas c pack MULTI or empty pre-labeled cobas c packs. The ICVC feature allows the reagent probe to dive into the reagent cassette and confirm the reagent level in the bottles. This ensures

Details

Units Affected
76 units
Distribution
USA Nationwide Distribution including San Juan PR
Location
Indianapolis, IN

Frequently Asked Questions

What product was recalled?
Cobas c8000 Modular Analyzer Series Cobas c502, Part Number 5964067001, a clinical chemistry analyzer intended for the in vitro quantitative / qualitative determination of analytes in body fluids.. Recalled by Roche Diagnostics Operations, Inc.. Units affected: 76 units.
Why was this product recalled?
The Initial Cassette Volume Check (ICVC) is not activated on the cobas c 502 module of the cobas 8000 modular analyzer series when manually filled cobas c packs are loaded. This issue occurs with tests that use cobas c pack MULTI or empty pre-labeled cobas c packs. The ICVC feature allows the reagent probe to dive into the reagent cassette and confirm the reagent level in the bottles. This ensures
Which agency issued this recall?
This recall was issued by the FDA Devices on April 16, 2014. Severity: Moderate. Recall number: Z-1449-2014.