A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Reumofan Plus: Recall – Undeclared Drug Ingredient. According to the Food & Drug Administration FDA’s MedWatch:
Product contains potentially harmful active pharmaceutical ingredients that may interact with other medications and result in serious adverse events.
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: Reumofan Plus: Recall – Undeclared Drug Ingredient.
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.