Teva Pharmaceuticals USA, Inc Recall: Nortrel (norethindrone and ethinyl estradiol tablets
Teva Pharmaceuticals USA, Inc Recall: Nortrel (norethindrone and ethinyl estradiol tablets is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Teva Pharmaceuticals USA, Inc; Product: Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35, packaged in cartons, each carton contains
| Recalling firm | Teva Pharmaceuticals USA, Inc |
|---|---|
| Product | Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35, packaged in cartons, each carton contains 3 blister cards, each card contains 28 tablets, Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0555-9008-67 |
| Reason for recall | Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets. |
| Classification | Class III (least serious — unlikely to cause adverse health consequences) |
| Status | Ongoing |
| Distribution | nationwide |
| Recall initiated | 20240125 |
| Recall number | D-0321-2024 |
| Category | drug |
| State | NJ |
| Country | United States |
$29/mo
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