CytoCell DiGeorge/VCFS TUPLE1 Region and 22q13.3 Region recall
CytoCell DiGeorge/VCFS TUPLE1 Region and 22q13.3 Region Probe, Model Number LPU004-A. analyte specific reagent for in vitro diagnostics
Why was CytoCell DiGeorge/VCFS TUPLE1 Region and 22q13.3 Region recalled?
The device may show unexpected locus specific signals in addition to those at 22q. Users may observe faint additional locus specific signals at 20p12/13.
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: 071399 072985
- Product
- CytoCell DiGeorge/VCFS TUPLE1 Region and 22q13.3 Region Probe, Model Number LPU004-A. analyte specific reagent for in vitro diagnostics
- Recalling firm
- Cytocell Ltd.
- Quantity
- 50
- Distribution
- Distribution to US states of CA, IL, MO, NY, PA, TX, and UT, and Canada.
- Recall date
- August 4, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)