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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

Vital Care Compounder C-Semaglutide Injection Recalled for Sterility Concerns

Agency Publication Date: April 19, 2023
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Summary

Pharmacy Plus, Inc. dba Vital Care Compounder has recalled 45 vials of C-Semaglutide (semaglutide) 5mg/mL injection because of a lack of assurance of sterility. This means the injectable medication may not be free from microorganisms, which is required for patient safety. The recall affects 0.5mL vials labeled with lot number 73810 and an expiration date of May 1, 2023.

Risk

Injecting a product that is not sterile can lead to serious or life-threatening infections at the site of injection or in the bloodstream. If these injections were used, there is a risk of localized inflammation or systemic illness.

What You Should Do

  1. This recall affects Vital Care Compounder C-Semaglutide 5mg/mL injection (0.5mL vials) labeled with lot number 73810 and an expiration date of 5/1/2023.
  2. If you have health concerns, contact your healthcare provider or pharmacist.
  3. Return any unused product to the place of purchase for a refund, throw it away, or contact Pharmacy Plus, Inc. dba Vital Care Compounder for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional information.

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: C-Semaglutide 5mg/mL injection (0.5mL vials)
Variants: 0.5mL vials, Rx only
Lot Numbers:
73810 (Exp. 5/1/2023)

Quantity: 45 vials

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92121
Status: Active
Manufacturer: Pharmacy Plus, Inc. dba Vital Care Compounder
Sold By: Pharmacy Plus, Inc.; Vital Care Compounder
Manufactured In: United States
Units Affected: 45 vials
Distributed To: Mississippi

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.