Teva Pharmaceuticals USA recalls Mimvey (estradiol and norethindrone acetate) 1 mg/0.5 mg tablets due to mislabeling. Affected lots expire 03/2022 to 01/2023. No remedy specified in recall notice.
Mislabeling
Teva Pharmaceuticals USA is recalling Mimvey (estradiol and norethindrone acetate) 1 mg/0.5 mg tablets because of mislabeling. This could lead to incorrect dosing if the product is used without proper identification.
Mislabeling means the product may not be correctly identified, which could lead to incorrect dosing if the patient takes the tablets without knowing the right dosage. This is a labeling issue that affects prescription safety.
Prescription patients who have the specific lot numbers of Mimvey tablets (100018610, 100021521, 100024575) from the listed expiration dates. Patients using the product without proper identification may face incorrect dosing.
Check the lot number on the carton: 100018610 (expires 03/2022), 100021521 (expires 09/2022), or 100024575 (expires 01/2023). The product is a prescription-only tablet with NDC 0093-5455-42.
Look for the lot numbers 100018610, 100021521, or 100024575 on the carton to determine if the product is affected.
The recall is due to mislabeling, which could lead to incorrect dosing if the product is used without proper identification. The product is not safe to use without verifying the lot number.
The recall notice does not specify a remedy, so there is no action required beyond checking the lot number to ensure you have the correct product.
Check the lot number on the carton: 100018610 (expires 03/2022), 100021521 (expires 09/2022), or 100024575 (expires 01/2023).
We’ve drafted a message you can send Teva Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0522-2022 — Teva Pharmaceuticals Teva Pharmaceuticals Hello, I own a Teva Pharmaceuticals that is covered by recall D-0522-2022 from Teva Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
