PlainRecalls
FDA Devices Moderate Class II Terminated

cobas e 601 module (cobas 6000 Modular Series system) Part Number: 04745922001

Reported: September 11, 2019 Initiated: July 18, 2019 #Z-2476-2019

Product Description

cobas e 601 module (cobas 6000 Modular Series system) Part Number: 04745922001

Reason for Recall

Quality issue with high pressure solenoid valves may cause inaccurate results.

Details

Units Affected
1 unit
Distribution
State NY MT HI IN MD TX OH KS KY CA FL OR LA MO AK
Location
Indianapolis, IN

Frequently Asked Questions

What product was recalled?
cobas e 601 module (cobas 6000 Modular Series system) Part Number: 04745922001. Recalled by Roche Diagnostics Operations, Inc.. Units affected: 1 unit.
Why was this product recalled?
Quality issue with high pressure solenoid valves may cause inaccurate results.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 11, 2019. Severity: Moderate. Recall number: Z-2476-2019.