Cytocell RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory recall — FDA Z-2210-2023
DNAs used during the manufacture of two affected models were accidentally inverted during manufacturing.
Overview of recall records associated with Cytocell Ltd., including dates, categories and classifications where available.
Classification mix: Class II: 2.
DNAs used during the manufacture of two affected models were accidentally inverted during manufacturing.
DNAs used during the manufacture of two affected models were accidentally inverted during manufacturing.
This page summarizes recall records in which the official source identifies Cytocell Ltd. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.