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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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Critical RiskFDA Drug
Medications & Supplements/Over-the-Counter

Hellolife: Homeopathic OTC Medicines Recalled for Microbial Contamination

Agency Publication Date: September 12, 2018
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Summary

Approximately 7,586 bottles of four different HelloLife homeopathic OTC medicines—Compulsin, Neuroveen, Thyroveev, and Respitrol—have been voluntarily recalled due to microbial contamination. The products were found to contain microorganisms including Staphylococcus saprophyticus and Burkholderia cepacia, which can lead to serious infections. These 2 fl oz (59 mL) bottles were distributed nationwide in the USA and to dozens of other countries between March 2017 and August 2018.

Risk

The presence of Staphylococcus saprophyticus and Burkholderia cepacia in these non-sterile liquid products poses a risk of infection, particularly for consumers with weakened immune systems or those with underlying health conditions. Burkholderia cepacia, in particular, is known to cause serious respiratory infections in vulnerable populations.

What You Should Do

  1. Check your medicine cabinet for 2 fl oz (59 mL) bottles of Compulsin (NDC 49726-034-02), Neuroveen (NDC 49726-015-02), Thyroveev (NDC 49726-025-02), or Respitrol (NDC 49726-003-02).
  2. Verify the lot numbers and expiration dates on the bottle labels: look for Compulsin lot CO/030717B, Neuroveen lot NV/030717D, Thyroveev lot TV/030717F, or Respitrol lot RE/030717E, all with an expiration date of 7/2019.
  3. Immediately stop using any affected medication if you identify a recalled lot in your possession.
  4. Contact your healthcare provider or pharmacist for guidance regarding any health concerns or if you have already used the contaminated product.
  5. Return any unused product to the place of purchase for a refund and contact Hellolife at their Grand Rapids, Michigan location for further instructions.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund

Healthcare provider consultation and pharmacy refund.

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

Affected Products

Product: Compulsin, Homeopathic (OTC Medicine) (2 fl oz / 59 mL)
Model:
NDC: 49726-034-02
Recall #: D-1200-2018
Lot Numbers:
CO/030717B (Exp 7/2019)
Date Ranges: 7/2019
Product: Neuroveen, Homeopathic (OTC Medicine) (2 fl oz / 59 mL)
Model:
NDC: 49726-015-02
Recall #: D-1201-2018
Lot Numbers:
NV/030717D (Exp 7/2019)
Date Ranges: 7/2019
Product: Thyroveev, Homeopathic (OTC Medicine) (2 fl oz / 59 mL)
Model:
NDC: 49726-025-02
Recall #: D-1202-2018
Lot Numbers:
TV/030717F (Exp 7/2019)
Date Ranges: 7/2019
Product: Respitrol, Homeopathic (OTC Medicine) (2 fl oz / 59 mL)
Model:
NDC: 49726-003-02
Recall #: D-1203-2018
Lot Numbers:
RE/030717E (Exp 7/2019)
Date Ranges: 7/2019

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 80893
Status: Resolved
Manufacturer: Hellolife
Sold By: Hellolife, Inc.
Manufactured In: United States
Units Affected: 4 products (989 bottles; 4,358 bottles; 370 bottles; 1,869 bottles)
Distributed To: Nationwide
Agency Last Updated: September 17, 2018

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.

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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 · 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.