traZODone Hydrochloride Tablets, USP, 50 mg, Rx only, 100… was recalled on August 24, 2026 in cooperation with the U.S. Food and Drug Administration because presence of Foreign Tablets/Capsules.
traZODone Hydrochloride Tablets, USP, 50 mg, Rx only, 100 Tablets, Manufactured in Croatia By: Pliva Hrvatska d.o.o, Zagreb, Croatia, Manufactured For: Teva Pharmaceuticals, Parsippany, NJ 07054, NDC 50111-560-01
Lot: 1394026, Exp. 02/2028.
Units affected: 175,392 bottles
Where it was sold: U.S. Nationwide
Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.
Presence of Foreign Tablets/Capsules
Class II means the product might cause a temporary or medically reversible health problem; the chance of serious harm is remote.
Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.
Contact: Recalling firm: Teva Pharmaceuticals USA, Inc
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Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.
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