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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

IntegraDose Vasopressin Injection Recalled for Subpotency

Agency Publication Date: September 30, 2024
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Summary

IntegraDose Compounding Services LLC is recalling 281 syringes of Vasopressin (2 Unit/2 mL in 0.9% Sodium Chloride). This injectable medication is being recalled because it was found to be subpotent, meaning it contains less of the active drug than specified. The recall involves 2 mL syringes labeled with lot number 20230921VAS-2 and an expiration date of March 19, 2024.

Risk

A subpotent drug may fail to provide the intended therapeutic effect. For a medication like Vasopressin, this could result in inadequate blood pressure support or ineffective treatment of fluid balance disorders.

What You Should Do

  1. This recall affects Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride, 2 mL per syringe (NDC 71139-0190-1), labeled for IntegraDose Compounding Services LLC. Affected units are marked with Lot 20230921VAS-2 and an expiration date of 03/19/2024.
  2. Stop using the recalled product immediately.
  3. Contact IntegraDose Compounding Services LLC or your distributor to arrange for the return of any remaining syringes.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional information.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride (2 mL per syringe)by IntegraDose
Variants: 2 Unit/2 mL, 0.9% Sodium Chloride, Syringe, Rx Only
Lot Numbers:
20230921VAS-2 (Exp. Date 03/19/2024)
NDC:
71139-0190-1

Quantity: 281 syringes; Manufactured in Minneapolis, MN.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93829
Status: Active
Manufacturer: IntegraDose Compounding Services LLC
Sold By: Hospitals; Clinics
Manufactured In: United States
Units Affected: 281 syringes
Distributed To: Minnesota

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.