Liquid Cardiac Control recall
Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053
Why was Liquid Cardiac Control recalled?
Customers may observe a decrease in recovered concentration with regards to NTproBNP in the Liquid Cardiac Control lots identified, on the Siemens Dimension EXL LOCI.
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?
lots 4243CK, 4244CK, 4245CK.
- Product
- Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053
- Recalling firm
- Randox Laboratories Ltd.
- Quantity
- 11420 kits
- Distribution
- Product distributed to CA, DE, WV, and Puerto Rico.
- Recall date
- June 26, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)