Teva Pharmaceuticals USA Recall: Mimvey Lo (estradiol and norethindrone acetate tablets US
Teva Pharmaceuticals USA Recall: Mimvey Lo (estradiol and norethindrone acetate tablets US is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Teva Pharmaceuticals USA; Product: Mimvey Lo (estradiol and norethindrone acetate tablets USP), 0.5 mg/0.1 mg, 28 tablets per blister card (NDC 009
| Recalling firm | Teva Pharmaceuticals USA |
|---|---|
| Product | Mimvey Lo (estradiol and norethindrone acetate tablets USP), 0.5 mg/0.1 mg, 28 tablets per blister card (NDC 0093-5454-18), packaged in 3 blister cards per carton (NDC 0093-5454-62), Rx only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970; Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA 18960. |
| Reason for recall | Failed Impurities/Degradation Specifications: out of specification test results for the norethindrone impurity. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide in the United States |
| Recall initiated | 20170202 |
| Recall number | D-0479-2017 |
| Category | drug |
| State | PA |
| Country | United States |
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