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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

MPRX, Inc. dba Medical Park Pharmacy: Compounded Medications Recalled for Incorrect Labeling and Expired Components

Agency Publication Date: January 29, 2020
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Summary

MPRX, Inc. (dba Medical Park Pharmacy) is recalling 57 units of various compounded medications, including hormones, topical creams, and supplements, because they may have incorrect or missing expiration dates and lot numbers. Additionally, some of these products were made using ingredients that had already expired at the time of production. Consumers who have these medications should not use them and instead contact their healthcare provider or the pharmacy directly.

Risk

Using medications with expired ingredients or incorrect dating can result in the drugs being less effective or potentially unsafe, as the stability and potency of the medicine cannot be guaranteed. No injuries or adverse events have been reported to date, but the use of expired components violates safety standards for sterile and non-sterile compounding.

What You Should Do

  1. Check your medication packaging for any of the following products: DHEA/Pregnenol One, Finasteride/Biotin, Lidocaine/Prilocaine creams, Liothyronine (T3), Magic Bullet Supplement, Naltrexone, Progesterone, Sildenafil, Squaric Acid, T3/T4 capsules, Tadalafil, or Testosterone Topical Cream.
  2. Locate the lot number and 'Use by' date on your product label and compare it against the affected list, which includes lot numbers such as L61406, 60658, 61367, 61134, 61302, 61318, 61253, 61024, 61048, 60564, 61242, 61215, 61219, 61392, 61404, 61380, 61296, 61137, 61324, 60856, 61229, and 61463.
  3. If your medication matches an affected lot or has a 'Use by' date between December 28, 2019, and May 6, 2020, stop using the medication immediately.
  4. Contact your healthcare provider or pharmacist to discuss alternative treatments and to report any side effects or concerns related to the use of these recalled medications.
  5. Return any unused portion of the recalled medication to Medical Park Pharmacy at 8230 Elmbrook Dr Ste 600b, Dallas, Texas, 75247 for a refund.
  6. For further questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Product return for credit/refund

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

Affected Products

Product: DHEA/Pregnenol One 10.25 MG Cap
Model:
D-0803-2020
Lot Numbers:
L61406:42 (Use by: 05/06/2020)
Date Ranges: 05/06/2020
Product: Finasteride/Biotin 1 mg/50 mcg
Model:
D-0804-2020
Lot Numbers:
60658:42 (Use by: 12/28/2019)
Date Ranges: 12/28/2019
Product: Lidocaine/Priloc/PE 15/5/0.25% 30 GM jars
Model:
D-0805-2020
Lot Numbers:
61367:42 (Use by: 04/28/2020)
Date Ranges: 04/28/2020
Product: Lidocaine/Priloc/PE 30/5/0.25% 30 GM jars
Model:
D-0806-2020
Lot Numbers:
61134:42 (Use by: 01/31/2020)
61302:26 (Use by: 04/14/2020)
61318:42 (Use by: 04/19/2020)
Date Ranges: 01/31/2020, 04/14/2020, 04/19/2020
Product: Liothyronine (T3) 80 mcg SR cap
Model:
D-0807-2020
Lot Numbers:
61253:42 (Use by: 04/01/2020)
Date Ranges: 04/01/2020
Product: Liothyronine (T3) 92.5 MCG
Model:
D-0808-2020
Lot Numbers:
61024:99 (Use by: 02/20/2020)
Date Ranges: 02/20/2020
Product: Magic Bullet Supplement
Model:
D-0809-2020
Lot Numbers:
61048:99 (Use by: 02/08/2020)
Date Ranges: 02/08/2020
Product: Naltrexone 4.5 mg capsule
Model:
D-0810-2020
Lot Numbers:
60564:42 (Use by: 02/10/2020)
Date Ranges: 02/10/2020
Product: Progesterone 200 mg Troche
Model:
D-0811-2020
Lot Numbers:
61242:26 (Use by: 02/28/2020)
Date Ranges: 02/28/2020
Product: Progesterone 50 mg capsules
Model:
D-0812-2020
Lot Numbers:
61215:26 (Use by: 03/23/2020)
Date Ranges: 03/23/2020
Product: Progesterone E4M SR 100 mg capsules
Model:
D-0813-2020
Lot Numbers:
61219:42 (Use by: 03/24/2020)
Date Ranges: 03/24/2020
Product: Sildenafil 200 mg Troche (Clinic)
Model:
D-0814-2020
Lot Numbers:
61392:42 (Use by: 05/05/2020)
Date Ranges: 05/05/2020
Product: Sildenafil 80 mg capsules
Model:
D-0815-2020
Lot Numbers:
61404:42 (Use by: 05/06/2020)
Date Ranges: 05/06/2020
Product: Squaric Acid 0.1% Topical Solution (Clinic) 30 mL
Model:
D-0816-2020
Lot Numbers:
61380:42 (Use by: 05/04/2020)
Date Ranges: 05/04/2020
Product: T3/T4 SR 9 mcg/38 mcg capsule
Model:
D-0817-2020
Lot Numbers:
61296:42 (Use by: 04/13/2020)
Date Ranges: 04/13/2020
Product: Tadalafil 20 mg Troche
Model:
D-0818-2020
Lot Numbers:
61137:42 (Use by: 03/08/2020)
61324:99 (Use by: 04/04/2020)
60856:42 (Use by: 02/02/2020)
Date Ranges: 03/08/2020, 04/04/2020, 02/02/2020
Product: Tadalafil 6 mg Capsule
Model:
D-0819-2020
Lot Numbers:
61229:26 (Use by: 03/25/2020)
61229:42 (Use by: 03/25/2020)
Date Ranges: 03/25/2020
Product: Testosterone Topical Cream 4%
Model:
D-0820-2020
Lot Numbers:
61463:42 (Use by: 02/27/2020)
Date Ranges: 02/27/2020

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84527
Status: Resolved
Manufacturer: MPRX, Inc. dba Medical Park Pharmacy
Sold By: Medical Park Pharmacy
Manufactured In: United States
Units Affected: 18 products (1 bottle; 1 bottle; 2 jars; 12 jars; 5 bottles; 4 bottles; 1 bottles; 2 bottles; 1 bottle; 1 bottle; 3 bottles; 1 bottle; 1 bottle; 1 bottle; 2 bottles; 9 bottles; 7 bottles; 3 bottles)
Distributed To: Texas

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.