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Food & drug recall · FDADecember 19, 2025Labelling issue

Zydus Pharmaceuticals (USA) Inc — traZODONE Hydrochloride Tablets, USP, 100mg, 1,000 Tablets, Rx only

Do not stop taking this without speaking to your pharmacist or doctor.

What’s wrong

Failed Tablet/Capsule Specifications: Product complaint received that some tablets had a dent on the plain side of the tablet surface.

The Recall Registry rates this labelling issue — FDA Class III: unlikely to cause harm.

What to do

Check the lot numbers below against what you have. Do not stop taking a prescription medicine because of a recall without speaking to your pharmacist or doctor first — for many medicines stopping is more harmful than continuing, and they can tell you whether yours is affected and what to do about it.

Who to contact: Recalling firm: Zydus Pharmaceuticals (USA) Inc

The product

traZODONE Hydrochloride Tablets, USP, 100mg, 1,000 Tablets, Rx only, Manufactured by: Zydus Lifesciences Ltd., India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-806-10

Details

Units affected
2,136 1000-count bottles
Recall date
December 19, 2025
Brand
Zydus Pharmaceuticals (USA) Inc
Model, lot or SKU numbers
Lot # EA00237A, Exp Date: 04/30/2027
Where it was distributed

Nationwide in the USA

The official notice

This recall was issued by the U.S. Food and Drug Administration. The Recall Registry summarises it — always confirm the details at the source.

Their exact wording: “Zydus Pharmaceuticals (USA) Inc — traZODONE Hydrochloride Tablets, USP, 100mg, 1,000 Tablets, Rx only, Manufactured by: Zydus Lifesciences Ltd., India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-806-10”

Read it on FDA →

Worried about the other things in your house? You can write down what you have and be told if one is recalled — or, if you sell second-hand, check your whole stock at once.

Filed under: Prescription medicine

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