Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

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.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Complete Pharmacy and Medical Solutions, LLC.: Human Chorionic Gonadotropin Recalled for Lack of Potency Testing

Agency Publication Date: January 19, 2021
Share:
Sign in to monitor this recall

Summary

Complete Pharmacy and Medical Solutions, LLC. is recalling approximately 7,144 vials of Human Chorionic Gonadotropin (HCG) injections in four different strengths: 1,250 IU, 5,000 IU, 6,000 IU, and 11,000 IU. This recall was initiated due to Good Manufacturing Practice deviations, specifically because the vials were not tested for potency before being distributed. Consumers should contact their healthcare provider or pharmacist for guidance, as the actual strength of the medication may differ from what is listed on the label. All affected products were distributed nationwide and have a 'Use By' date of January 30, 2021.

Risk

Without proper potency testing, the medication may be stronger or weaker than intended. This lack of quality control can result in patients receiving an incorrect dose, which could lead to ineffective treatment or unexpected side effects.

What You Should Do

  1. Identify your product by checking the strength and lot number on the vial label. Affected vials include: 1,250 IU (Lot 40548), 5,000 IU (Lot 40570), 6,000 IU (Lot 40604), and 11,000 IU (Lot 40568).
  2. Verify the 'Use By' date on your packaging; all affected vials are marked with a 'Use By' date of 01/30/2021.
  3. Stop using any medication that matches these lot numbers immediately.
  4. Contact your healthcare provider or pharmacist to discuss your treatment and determine if a replacement medication is necessary.
  5. Return any unused vials to the place of purchase for a refund and contact Complete Pharmacy & Medical Solutions at 305-397-2035 for further instructions.
  6. For additional questions or to report a problem, contact the FDA Consumer Complaint line at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

๐Ÿ’ฐFull Refund

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

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund and contact the manufacturer at 305-397-2035 for further instructions.

Affected Products

Product: Human Chorionic Gonadotropin 11,000 IU per vial (Lyophilized, Unpreserved)
Model:
D-0234-2021
Lot Numbers:
40568
Date Ranges: Use By Date: 01/30/2021
Product: Human Chorionic Gonadotropin 6,000 IU per vial (Lyophilized, Unpreserved)
Model:
D-0235-2021
Lot Numbers:
40604
Date Ranges: Use By Date: 01/30/2021
Product: Human Chorionic Gonadotropin 5,000 IU per vial (Lyophilized, Unpreserved)
Model:
D-0236-2021
Lot Numbers:
40570
Date Ranges: Use By Date: 01/30/2021
Product: Human Chorionic Gonadotropin 1,250 IU per vial (Lyophilized, Unpreserved)
Model:
D-0237-2021
Lot Numbers:
40548
Date Ranges: Use By Date: 01/30/2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87076
Status: Resolved
Manufacturer: Complete Pharmacy and Medical Solutions, LLC.
Sold By: Pharmacies
Manufactured In: United States
Units Affected: 4 products (1182 vials; 2418 vials; 1144 vials; 2400 vials)
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.