A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Gris-PEG (griseofulvin ultramicrosize): Health Advisory – Risk of Product Mix-Up. According to the Food & Drug Administration FDA’s MedWatch:
During packaging and labeling, tablets from one product type may have carried over into packaging of another product.
For more information on the drug or medical device recall or safety alert, read the Food & Drug Administration’s FDA’s drug or medical device recall or safety alert: Gris-PEG (griseofulvin ultramicrosize): Health Advisory – Risk of Product Mix-Up.
To report an adverse reaction, problem or other issue with a drug or medical device, submit a drug or medical device complaint to the government at fda.gov or MedWatch.
If you have thoughts on the drug or medical device recall or safety alert, share your drug or medical device recall or safety alert comments below.