Cytocell Ltd.: Medical Device Recalls in 2019

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Cytocell Ltd. in 2019. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Aquarius CSF1R/RPS14 (5q32-q33) Probe Red, Model LPH540-A Analyte specific reagent.
Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb region including most of the DLEU2 gene, part of the DLEU1 gene and the D13S319 and D13S272 markers. The 13qter subtelomere specific probe, labelled in green, allows identification of chromosome 13 and acts as a control probe.