Medical DeviceMay 10, 2023
DERMLITE DL4W, REF: DL4W, Rx Only MD, CE recall — FDA Z-1506-2023
Incorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling.
Class IIFDA: OngoingDermLite LLC
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies DermLite LLC 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.