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Qualitest Pharmaceuticals Oral Contraceptives: Recall – Packaging Error

A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Qualitest Pharmaceuticals Oral Contraceptives: Recall – Packaging Error. According to the Food & Drug Administration FDA’s MedWatch:

Daily regimen may be incorrect and could leave women without adequate contraception.

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 Pharmaceuticals Oral Contraceptives: Recall – Packaging Error.

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.

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