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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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High RiskFDA Drug
Medications & Supplements/Prescription Drugs

Partell Specialty Pharmacy: Various Compounded Drugs Recalled for Sterility Concerns

Agency Publication Date: April 17, 2018
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Summary

Partell Specialty Pharmacy is recalling approximately 62 units of various compounded drug products, including injectable liquids and pellets such as Testosterone, Estradiol, and Vitamin D. These products were sterilized using a non-approved method, which means the pharmacy cannot guarantee they are completely free of germs or bacteria. The recall was initiated after a lack of sterility assurance was identified, though no specific patient injuries have been reported at this time. These medications were distributed exclusively in Nevada between late 2017 and early 2018.

Risk

Using a drug intended to be sterile that is not properly sterilized poses a high risk of serious infection. These infections can be life-threatening if the bacteria enters the bloodstream or deep tissues via injection or surgical implantation of pellets.

What You Should Do

  1. Identify if you have any affected products by checking the label for 'Partell Specialty Pharmacy' and the specific lot numbers and Beyond Use Dates (BUD). Examples include Testosterone pellets with lots like 20171128@9, Estradiol pellets like 20171201@84, or Vitamin D 50,000 unit/ml vials with lot 20180220@4.
  2. Immediately stop using any of the medications listed in this recall that you still have in your possession.
  3. Contact your healthcare provider or pharmacist immediately if you have used any of these products and are experiencing unusual symptoms or signs of infection.
  4. Return any unused vials or pellets to Partell Specialty Pharmacy at 5835 S. Eastern Ave. #101, Las Vegas, NV 89119, or contact them at (702) 791-3800 for instructions on obtaining a refund.
  5. For additional questions or to report a complaint, 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 for refund.

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

Affected Products

Product: Ascorbic Acid (Tapioca) 500 mg/mL (50 mL amber vial)
Model:
D-0634-2018
Lot Numbers:
20180201@34
20180202@56
20180129@41
20180207@16
Date Ranges: BUD 04/02/2018, BUD 04/03/2018, BUD 3/30/2018, BUD 04/08/2018
Product: B-complex (B1-200mg, B2-4mg, B3-200mg,B5-4mg,B6-4mg) /mL (5 mL amber vial)
Model:
D-0635-2018
Lot Numbers:
20180205@18
20180126@28
20180126@22
20180205@9
20180214@17
Date Ranges: BUD 04/06/2018, BUD 03/27/2018, BUD 04/14/2018
Product: Biotin Suspension 10mg/mL (5 mL amber vial)
Model:
D-0636-2018
Lot Numbers:
20180216@10
20180129@25
Date Ranges: BUD 5/17/2018, BUD 04/29/2018
Product: CoEnzymeQ10 25mg/mL (5mL amber vial)
Model:
D-0637-2018
Lot Numbers:
20171227@14
20180205@37
20180214@30
Date Ranges: BUD 03/27/2018, BUD 05/06/2018, BUD 05/15/2018
Product: Glutathione 200mg/mL (10mL amber vial)
Model:
D-0638-2018
Lot Numbers:
20180219@58
20180131@15
20180116@9
20180103@5
Date Ranges: BUD 05/20/2018, BUD 05/01/2018, BUD 04/14/2018, BUD 04/03/2018
Product: HCG 1000 units/mL (2 mL or 6 mL amber vial)
Model:
D-0639-2018
Lot Numbers:
20180219@6
20180207@14
0180214@22
20180220@7
Date Ranges: BUD 04/05/2018, BUD 03/24/2018, BUD 03/31/2018, BUD 04/06/2018
Product: Lipoic Acid 25mg/mL (5 mL amber vial)
Model:
D-0640-2018
Lot Numbers:
20180124@10
20180220@9
20180102@33
Date Ranges: BUD 04/05/2018, BUD 05/21/2018, BUD 04/02/2018
Product: Methionine15mg/Inositol 50mg/Choline 100mg (5mL or 50 mL amber vial)
Model:
D-0641-2018
Lot Numbers:
20180129@18
20171127@6
20180207@12
20180108@16
Date Ranges: BUD 04/14/2018
Product: Methionine 25mg/Inositol 50mg/Choline 50mg/ B12 1mg (5 mL or 50mL amber vial)
Model:
D-0642-2018
Lot Numbers:
20180123@9
20171222@11
20180214@7
20180221@3
20180214@6
Date Ranges: BUD 04/14/2018, BUD 08/14/2018, BUD 08/21/2018
Product: Nandrolone decanoate 200mg/mL (5 mL amber vial)
Model:
D-0643-2018
Lot Numbers:
20180221@15
20180123@10
Date Ranges: BUD 05/22/2018, BUD 04/23/2018
Product: Testosterone Cypionate 200mg/mL (5 mL amber vial)
Model:
D-0644-2018
Lot Numbers:
20180130@2
20180109@1
20180212@51
20171212@4
20180123@6
20171204@4
20171228@15
Date Ranges: BUD 7/29/2018, BUD 07/08/2018, BUD 08/11/2018, BUD 06/10/2018, BUD 07/22/2018, BUD 06/02/2018, BUD 03/28/2018
Product: Vitamin D 50,000 unit/ml (5 mL amber vial)
Model:
D-0646-2018
Lot Numbers:
20180220@4
20180221@14
20180228@1
Date Ranges: BUD 03/22/2018, BUD 03/23/2018, BUD 03/30/2018
Product: Testosterone 200 mg pellet
Model:
D-0662-2018
Lot Numbers:
20171128@9
20171201@74
20171211@68
20180209@62
20180219@5
20171010@11
20180212@102
Date Ranges: BUD 05/27/2018, BUD 08/08/2018, BUD 04/08/2018, BUD 08/11/2018
Product: Estradiol 10 mg (SD) pellets
Model:
D-0673-2018
Lot Numbers:
20171201@84
20180125@31
20180209@106
20171011@69
20171019@10
20171106@103
Date Ranges: BUD 05/30/2018, BUD 07/24/2018, BUD 08/08/2018, BUD 04/09/2018, BUD 04/17/2018, BUD 05/05/2018

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 79619
Status: Resolved
Manufacturer: Partell Specialty Pharmacy
Sold By: Partell Specialty Pharmacy
Manufactured In: United States
Units Affected: 17 products (4 vials; 5 vials; 2 vials; 3 vials; four vials; four vials; 11 vials; 2 vials; 7 vials; 15 vials; 4 vials; 1 vial; one vial; five vials; 1 vial; 7 vials; one vial)
Distributed To: Nevada

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.