FDA recall Z-0522-2025

Kreatech Biotechnology Bv · Class II · device

Product

Kreatech PapV-16, Flu labeled ISH probe, to detect presence of HPV-16 DNA inserts in human tissue, Model Number 40V016V495

Reason for recall

The DNA fragments for this specific lot number are too large, resulting in potential background around the cells due to suboptimal hybridization. An absence of signal could also be observed as a result of the suboptimal hybridization of the larger DNA fragments. The user may interpret potential background as a false positive result and an absence of signal as a false negative result, if proper positive and negative controls are not included.

Distribution

US States: FL, NY

Key facts

Status
Ongoing
Initiation date
2024-11-01
Report date
2024-12-04
Voluntary/Mandated
Voluntary: Firm initiated
Location
Amsterdam, Netherlands

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0522-2025