Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053
Reported: June 26, 2019 Initiated: March 11, 2019 #Z-1785-2019
Product Description
Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053
Reason for Recall
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.
Details
- Recalling Firm
- Randox Laboratories Ltd.
- Units Affected
- 11420 kits
- Distribution
- Product distributed to CA, DE, WV, and Puerto Rico.
- Location
- Crumlin (North), N/A
Frequently Asked Questions
What product was recalled? ▼
Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053. Recalled by Randox Laboratories Ltd.. Units affected: 11420 kits.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 26, 2019. Severity: Moderate. Recall number: Z-1785-2019.
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