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Diovan 160 mg, 90 tablets, Rx only Recall 2026

DIOVANIssued August 4, 2026Updated Reviewed by the Recall Watch editorial team

DIOVAN Diovan (valsartan) 160 mg, 90 tablets, Rx only, Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834, Distributed by: Novartis Pharmaceutical Corp, East Hanover, NJ 07936, NDC 007 — recalled per FDA on 8/4/2026. Reason: Failed Dissolution Specifications.

Agency
FDA
Issued
Aug 4, 2026
Brand
DIOVAN
Distribution
1 states
Lots affected
2
What to do right now

Steps to take for this recall

  1. Stop using it

    Take it out of rotation. Don't consume, wear, or operate.

  2. Verify the match

    Compare lot numbers, UPCs, and dates against your product.

  3. Return or dispose

    Follow the manufacturer's instructions to refund or safely dispose.

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Verified summary of the official U.S. Food and Drug Administration notice · Issued August 4, 2026 · Last synced Nov 1, 2026

What's recalled

Diovan (valsartan) 160 mg, 90 tablets, Rx only, Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834, Distributed by: Novartis Pharmaceutical Corp, East Hanover, NJ 07936, NDC 0078-0359-34

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Why it was recalled

Failed Dissolution Specifications

Affected products & lot numbers
2 lots called out

Affected Lot Numbers

Check your product label — do not use if your lot number appears below.

Lot Number
Lot AV5913C
Expiry: 6/2027
Where was it sold
1 state

US Nationwide

nationwide
Official noticefda.gov
More recalls like this
4 related — by brand, contaminant, and category

Frequently asked questions

Is the DIOVAN recall still active?

Yes, this recall is currently active as of August 4, 2026. Do not use or consume the affected product.

What lot numbers are affected?

Affected lot numbers: Lot AV5913C, Expiry: 6/2027. Check the label on your product.

What should I do if I have the recalled DIOVAN?

Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.