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Recall Observatory FDA recall evidence

Device product

cobas e801 Immunoassay Analyzer

Z-1515-2022

July 14, 2022

Class II

Product summary

Firm
Roche Diagnostics Operations, Inc.
Event
Event 90657
Status
Ongoing
Classification
Class II
Quantity
965 units
Official record key
device-enforcement:Z-1515-2022

Official wording

Reason: 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.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    Software issue