FDA recall Z-0969-2018
Randox Laboratories · Class III · device
Product
Immunoassay Premium Controls (3x4x5mL and 12x5mL packages)
Reason for recall
The ACTH in Immunoassay Premium and Premium Plus quality control does not meet the quoted reconstituted stability claim in the product IFU.
Distribution
Distribution US nationwide.
Key facts
- Status
- Terminated
- Initiation date
- 2017-08-11
- Report date
- 2018-03-21
- Termination date
- 2019-03-29
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Kearneysville, WV, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0969-2018