FDAMarch 20, 2023device
DERMLITE DL4W, REF: DL4W, Rx Only MD, CE
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Incorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling.
What to do
FDA enforcement status: Ongoing
Brands named
dermlite
Recall history
No related federal recalls on record for this brand yet.
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