FDA Device recall Z-3015-2018
NEXES VEN IVIEW DAB DET KT JPN-US EXPORT, Catalog Number 05266084001 Model 760-041 Immunohistochemistry (IHC) for in vitro diagnostic use
- FDA Device
- Class I
- terminated
- Published 2018-09-26
On 2018-09-26 the FDA classified a Class I recall of NEXES VEN IVIEW DAB DET KT JPN-US EXPORT, Catalog Number 05266084001 Model 760-041 Immunohistochemistry (IHC) for in vitro diagnostic use by Ventana Medical Systems, citing leaking and sticking reagent dispensers for horseradish peroxidase (HRP) dispensers. A false negative IHC result may occur.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3015-2018 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2018-08-02 |
| Published | 2018-09-26 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ventana Medical Systems |
| Distribution | n/a |
Product
NEXES VEN IVIEW DAB DET KT JPN-US EXPORT, Catalog Number 05266084001 Model 760-041 Immunohistochemistry (IHC) for in vitro diagnostic use.
Reason
Leaking and sticking reagent dispensers for horseradish peroxidase (HRP) dispensers. A false negative IHC result may occur.
Identifiers
| code_info | Lot Numbers: Y22285, Y25750. UDI: 4015630970254 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3015-2018%22
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