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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

Matthew 7:25 Inc dba Thrive Pharmacy: Various Buprenorphine and Buprexone Troches Recalled for Subpotency

Agency Publication Date: March 23, 2020
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Summary

Matthew 7:25 Inc, doing business as Thrive Pharmacy, is recalling 563 units of Buprexone and Buprenorphine troches (medicated lozenges) because they are subpotent, meaning they contain less of the active medication than intended. The recall affects three specific products: Buprexone Banana cream (6-0.6 mg), Buprenorphine Watermelon (8 mg), and Buprenorphine Black Cherry (2 mg), which were sold in plastic molds with cardboard sleeves. These medications were distributed to patients in Florida between September 2019 and March 2020.

Risk

Subpotent medications provide a lower dose than what was prescribed by a physician, which can lead to the return of symptoms or withdrawal for patients relying on these treatments. This issue was identified as a moderate risk by the FDA, as inconsistent dosing of these specific medications can interfere with ongoing medical treatment plans.

What You Should Do

  1. Check your medication packaging for 'Thrive Pharmacy' located at 2863 St Johns Bluff RD. South # 135, Jacksonville, Florida.
  2. Identify if you have any of the following affected lots: Buprexone Banana cream Lot 190918B (Exp. 03/16/2020), Buprenorphine Watermelon Lot 191203F (Exp. 05/31/2020), or Buprenorphine Black Cherry Lot 191217A (Exp. 06/14/2020).
  3. If you possess any of these recalled troches, contact your healthcare provider or pharmacist immediately to discuss your treatment and obtain a replacement prescription.
  4. Return any remaining unused medication to Thrive Pharmacy for a refund and further instructions.
  5. For additional questions or to report any adverse effects, 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

Affected Products

Product: Buprexone Banana cream 6-0.6 mg Troche
Model:
D-1052-2020
Lot Numbers:
190918B (Exp. 03/16/2020)
Date Ranges: 03/16/2020
Product: Buprenorphine Watermelon 8 mg Troche
Model:
D-1053-2020
Lot Numbers:
191203F (Exp. 05/31/2020)
Date Ranges: 05/31/2020
Product: Buprenorphine Black Cherry 2 mg Troche
Model:
D-1054-2020
Lot Numbers:
191217A (Exp. 06/14/2020)
Date Ranges: 06/14/2020

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 85207
Status: Resolved
Manufacturer: Matthew 7:25 Inc dba Thrive Pharmacy
Sold By: Thrive Pharmacy
Manufactured In: United States
Units Affected: 3 products (71 troches; 403 troches; 89 troches)
Distributed To: Florida

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.