ISH iVIEW Blue Plus Detection Kit recall
ISH iVIEW Blue Plus Detection Kit, Catalog Number 05266181001, model 760-097 Immunohistochemistry (IHC) for in vitro diagnostic use.
Why was ISH iVIEW Blue Plus Detection Kit recalled?
Leaking and sticking reagent dispensers for horseradish peroxidase (HRP) dispensers. A false negative IHC result may occur.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Numbers: Y15410, Y24365 UDI: 4015630972029
- Product
- ISH iVIEW Blue Plus Detection Kit, Catalog Number 05266181001, model 760-097 Immunohistochemistry (IHC) for in vitro diagnostic use.
- Recalling firm
- Ventana Medical Systems Inc
- Quantity
- 2136 units
- Distribution
- worldwide
- Recall date
- September 26, 2018
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)