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Cytocell Ltd.: Medical Device Recalls in 2021

Updated on March 25, 2026.

According to to data from the FDA, there were 4 medical device recalls made by Cytocell Ltd. in 2021. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2019
2020
2021
2022
2023
  • Cytocell LPH019-A E2A (TCF3) Breakapart Probe- In Vitro Diagnostic Analyte specific reagents (ASR's)
  • Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte Specific Reagents. Model: MPA3481
  • Aquarius LPH 511-A CRLF2 Distal Probe Green, model no. LPH 511-A The CRLF2 Distal probe, labelled in green, consists of two probes (71kb and 131kb) that are situated distal (telomeric) to the CRLF2 gene
  • CytoCell DiGeorge/VCFS TUPLE1 Region and 22q13.3 Region Probe, Model Number LPU004-A. analyte specific reagent for in vitro diagnostics
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