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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 Sterile Syringes Recalled for Sub-potency

Agency Publication Date: February 15, 2024
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Summary

IntegraDose Compounding Services LLC has recalled 1,299 syringes of Vasopressin (2 Units/2 mL) in 0.9% Sodium Chloride. These compounded sterile syringes for injection were found to be sub-potent, meaning they may fail to maintain their required strength through the duration of their labeled expiration dates. This recall specifically affects medication distributed to healthcare facilities in Minnesota for office use only.

Risk

A sub-potent medication may not provide the necessary therapeutic effect to a patient. In clinical settings where vasopressin is used to maintain blood pressure, an ineffective dose could lead to inadequate treatment of life-threatening conditions.

What You Should Do

  1. This recall affects Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride Sterile Syringes for Injection (Concentration: 1 Unit/mL) sold in 2 mL syringes under NDC 71139-0190-1.
  2. Check for lot numbers 20230929VAS-2 (Exp. 02/29/2024), 20231004VAS-2 (Exp. 04/01/2024), 20231010VAS-2 (Exp. 04/07/2024), and 20231013VAS-2 (Exp. 04/10/2024).
  3. Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action

Clinical or hospital-administered drug return

How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride Sterile Syringe for Injection
Variants: Concentration: 1 Unit/mL, 2 mL Syringe, Rx Only
Lot Numbers:
20230929VAS-2 (Exp. 02/29/2024)
20231004VAS-2 (Exp. 04/01/2024)
20231010VAS-2 (Exp. 04/07/2024)
20231013VAS-2 (Exp. 04/10/2024)
NDC:
71139-0190-1

Compounded Drug Not for Resale. Office Use Only. Manufactured at 719 Kasota Ave SE, Minneapolis, MN.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93940
Status: Active
Manufacturer: IntegraDose Compounding Services LLC
Sold By: Healthcare facilities; Hospitals; Clinics
Manufactured In: United States
Units Affected: 1,299 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.