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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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Low RiskFDA Drug
Medications & Supplements/Prescription Drugs

Pharmedium Services, LLC: Vasopressin Injection Recalled for Manufacturing Practice Deviations

Agency Publication Date: April 17, 2018
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Summary

Pharmedium Services, LLC has recalled 72 bags of Vasopressin (0.2 units per mL) added to 0.9% Sodium Chloride Injection USP. This prescription medication is being recalled due to deviations from Current Good Manufacturing Practice (cGMP) requirements. While no specific patient injuries or incidents have been reported, consumers who have this product should immediately contact their healthcare provider or pharmacist for guidance.

Risk

The recall is due to manufacturing process deviations which could potentially compromise the quality, safety, or efficacy of the medication. Because this is an injectable drug, adherence to strict manufacturing standards is critical to ensure patient safety.

What You Should Do

  1. Check your medication bags for the product name 'Vasopressin 50 Units added to 250 mL 0.9% Sodium Chloride Injection USP' (0.2 units per mL).
  2. Verify the lot number and expiration date on the product label; this recall specifically affects Lot: 180660057S with an expiration date of 6/5/2018.
  3. If you identify an affected product, contact your healthcare provider or pharmacist immediately for guidance on using an alternative supply.
  4. Return any unused product bags from this specific lot to the pharmacy or medical facility where they were obtained for a refund.
  5. Contact Pharmedium Services, LLC for further instructions regarding this recall.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Contact healthcare provider and return product

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

Affected Products

Product: Vasopressin 50 Units added to 250 mL 0.9% Sodium Chloride Injection USP (0.2 units per mL)
Model:
Recall #: D-0632-2018
Lot Numbers:
180660057S (Exp. 6/5/2018)
Date Ranges: Exp. 6/5/2018

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 79799
Status: Resolved
Manufacturer: Pharmedium Services, LLC
Sold By: Hospital/Healthcare Providers
Manufactured In: United States
Units Affected: 72 bags
Distributed To: Massachusetts, Washington

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.