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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Avet Desmopressin Acetate Tablets Recalled for Subpotency

Agency Publication Date: November 29, 2022
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Summary

Heritage Pharmaceuticals Inc. is recalling 13,805 bottles of Desmopressin Acetate Tablets 0.2mg, which were distributed by Avet Pharmaceuticals Inc. The recall was initiated because the tablets were found to be subpotent, meaning they contain less of the active medication than is required by quality standards. Consumers using these tablets should consult their healthcare provider or pharmacist to discuss their treatment and obtain a replacement, as the subpotent medication may not be effective. No injuries or medical incidents have been reported to date regarding this issue.

Risk

Because the tablets are subpotent, patients may not receive the full intended dose of desmopressin acetate. This can lead to ineffective treatment of serious conditions like diabetes insipidus or bedwetting, potentially causing symptoms to worsen or return.

What You Should Do

  1. This recall affects 100-count bottles of Desmopressin Acetate Tablets 0.2mg (NDC 23155-490-01) with lot number 220440A and an expiration date of 05/2024.
  2. If you have health concerns or are currently taking this medication, contact your healthcare provider or pharmacist for guidance.
  3. Return any unused product to the place of purchase for a refund, throw it away, or contact Heritage Pharmaceuticals Inc. directly for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Desmopressin Acetate Tablets 0.2mg (100-count bottles)by Avet Pharmaceuticals Inc.
Variants: 0.2mg, 100-count bottle, Tablet, RX Only
Lot Numbers:
220440A (Exp 05/2024)
NDC:
23155-490-01

Distributed by Avet Pharmaceuticals Inc. Recall #: D-0072-2023.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 91171
Status: Resolved
Manufacturer: Heritage Pharmaceuticals Inc
Sold By: Avet Pharmaceuticals Inc.
Manufactured In: United States
Units Affected: 13805 Bottles each containing 100 tablets
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.