A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Qualitest Hydrocodone Bitartrate and Acetaminophen Tablets 10 mg/500 mg: Recall – Potential for Oversized Tablets. According to the Food & Drug Administration FDA’s MedWatch:
Tablets from the affected lot may exceed the weight specification and could be super-potent for the ingredients Hydrocodone Bitartrate and Acetaminophen.
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: Qualitest Hydrocodone Bitartrate and Acetaminophen Tablets 10 mg/500 mg: Recall – Potential for Oversized Tablets.
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.
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