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Recall Observatory FDA recall evidence

Device product

Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded Revogene: Catalog Number 610210 GenePOC branded Revogene: Catalog Number 130840

Z-0836-2022

February 15, 2022

Class II

Product summary

Firm
Meridian Bioscience Inc
Event
Event 89666
Status
Ongoing
Classification
Class II
Quantity
452 units (398 US, 54 OUS)
Official record key
device-enforcement:Z-0836-2022

Official wording

Reason: The photomultiplier tube, may have compromised functionality in some instruments. As a result, the user is likely to observe an increase in false-positive or indeterminate results.

Code information: UDI: 00840733102318 All units in the field, all serial numbers.

Distribution pattern: Worldwide distribution - US Nationwide distribution in the states of AK, AL, AR, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NV, NY, OH, OR, PA, PR, RI, SD, TN, TX, UT, VA, VT, WI, WV and the countries of Australia, Chile, Italy, Switzerland.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The photomultiplier tube, may have compromised functionality in some instruments. As a result, the user is likely to observe an increase in false-positive or indeterminate results.