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Roche Diagnostics Operations, Inc. recalls cobas e 601 module (cobas 6000 Modular Series system) Part Number: 04745922001
Recalled September 11, 2019 · FDA recall Z-2476-2019 · Roche Diagnostics Operations
Hazard
Quality issue with high pressure solenoid valves may cause inaccurate results. · FDA Class II
Units
1 unit
Sold at
State NY MT HI IN MD TX OH KS KY CA FL OR LA MO AK
Description
Quality issue with high pressure solenoid valves may cause inaccurate results.
Product
cobas e 601 module (cobas 6000 Modular Series system) Part Number: 04745922001
Manufacturer(s)
Roche Diagnostics Operations, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →