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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

Teva Pharmaceuticals USA: Desmopressin Acetate Tablets Recalled Due to Missing Desiccant

Agency Publication Date: February 6, 2020
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Summary

Teva Pharmaceuticals USA is recalling approximately 91,880 bottles of Desmopressin Acetate Tablets (0.1 mg and 0.2 mg strengths) because the product bottles may be missing a desiccant, which is a small packet or canister used to keep the medication dry. If the desiccant is missing, the tablets may be exposed to moisture, potentially causing the medicine to break down or lose its effectiveness. These 100-count bottles were sold nationwide to pharmacies across the United States.

Risk

Missing desiccant can allow moisture to degrade the active ingredients in the medication. This could lead to a decrease in the drug's potency, meaning it may not work effectively to treat the patient's condition as intended.

What You Should Do

  1. Check your prescription bottle label to see if you have Desmopressin Acetate Tablets in 0.1 mg or 0.2 mg strengths.
  2. For 0.1 mg tablets (NDC 0591-2464-01), check for lot numbers 1281203M (Exp. 03/2020) or 1290113M (Exp. 04/2020).
  3. For 0.2 mg tablets (NDC 0591-2465-01), check for lot numbers 1269726M (Exp. 01/2020), 1283269M (Exp. 03/2020), 1283270M (Exp. 03/2020), 1292992M (Exp. 04/2020), or 1292993A (Exp. 04/2020).
  4. Contact your healthcare provider or pharmacist for guidance on whether you should continue taking the medication or if you need a replacement.
  5. Return any affected unused medication to your place of purchase for a refund and contact Teva Pharmaceuticals USA at 1-888-838-2872 for additional instructions.
  6. Contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) if you have further questions.

Your Remedy Options

๐Ÿ’ฐFull Refund

Return to pharmacy for refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Desmopressin Acetate Tablets, 0.1 mg, 100-count bottle
Model:
0591-2464-01
Lot Numbers:
1281203M (Exp. 03/2020)
1290113M (Exp. 04/2020)
Date Ranges: 03/2020, 04/2020
Product: Desmopressin Acetate Tablets, 0.2 mg, 100-count bottle
Model:
0591-2465-01
Lot Numbers:
1269726M (Exp. 01/2020)
1283269M (Exp. 03/2020)
1283270M (Exp. 03/2020)
1292992M (Exp. 04/2020)
1292993A (Exp. 04/2020)
Date Ranges: 01/2020, 03/2020, 04/2020

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84798
Status: Resolved
Manufacturer: Teva Pharmaceuticals USA
Sold By: Pharmacies
Manufactured In: United States
Units Affected: 2 products (22,868 bottles; 69,012 bottles)
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.