device · product 1 of 1
cobas e801 Immunoassay Analyzer
- Recall number
- Z-1515-2022
- Initiated
- July 14, 2022
- Classification
- Class II
- Status
- Ongoing
- Recalling firm
- Roche Diagnostics Operations, Inc.
- Quantity
- 965 units
App-derived interpretation
Software issue
Official device-enrichment evidence · Sourced
Software design
Inspect official wording and provenance
Reason for recall
Software issue resulting in signals and sample test results of Pre-Wash tests being impacted. The following assays are considered impacted by the issue: Anti-HAV2, Anti-HBc IgM, IGF-1, Myogloin, Rubella IgG, and Toxo IgG.
Code information
UDI-DI: 07613336158456 and 04015630946198; Catalog No. 08454345001 and 07682913001. All serial numbers.
Distribution pattern
US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY, DC & PR.