ultraView Universal Alkaline Phosphatase Red Detection recall
ultraView Universal Alkaline Phosphatase Red Detection Kit, Catalog Number 05269814001, model 760-501 Immunohistochemistry (IHC) for in vitro…
Why was ultraView Universal Alkaline Phosphatase Red Detection 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: Y15071, Y18053, Y22469, UDI: 4015630972258
- Product
- ultraView Universal Alkaline Phosphatase Red Detection Kit, Catalog Number 05269814001, model 760-501 Immunohistochemistry (IHC) for in vitro…
- Recalling firm
- Ventana Medical Systems Inc
- Quantity
- 8211 units
- Distribution
- worldwide
- Recall date
- September 26, 2018
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)