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DermLite LLC recalls DERMLITE DL4W, REF: DL4W, Rx Only MD, CE
Recalled May 10, 2023 · FDA recall Z-1506-2023 · DermLite
Hazard
Incorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling. · FDA Class II
Units
32 units
Sold at
Worldwide - US Nationwide distribution in the states of CA, AZ, TX, FL, NE, IA, MO, CO and the countries of Saudi Arabia, Australia, Spain.
Description
Incorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling.
Product
DERMLITE DL4W, REF: DL4W, Rx Only MD, CE
Manufacturer(s)
DermLite LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →