ClearanceBrief
Recall Z-3014-2018 ยท MAQ Kit, Dna Detection, Human Papillomavirus

Ventana Medical Systems Inc

INFORM HPV III Fam 16 Probe - US Export, Catalog Number 05278856001, model 800-4295 Immunohistochemistry (IHC) for in vitro diagnostic use.

DateSep 14, 2018 (initiated Aug 2, 2018)
StatusTerminated
ReasonLeaking and sticking reagent dispensers for horseradish peroxidase (HRP) dispensers. A false negative IHC result may occur.
Root causeUnder Investigation by firm
ActionThe firm disseminated their field safety notices by letter on 08/02/2018. The firm requested the destruction of the product.
Quantity195 units
Distributionworldwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.