FDAFDA · Food and drugs·Recall number Z-2476-2019
cobas e 601 module (cobas 6000 Modular Series system) Part Number: 04745922001
Published September 11, 2019 · Recall initiated: July 18, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Quality issue with high pressure solenoid valves may cause inaccurate results.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Roche Diagnostics Operations, Inc.
- Distributor
- State NY MT HI IN MD TX OH KS KY CA FL OR LA MO AK
- Lot
- Serial # : 31A1-01
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.