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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

Magno Humphries Laboratories, Inc: Senna Laxative Recalled Due to Label Mix-Up with Naproxen Sodium

Agency Publication Date: February 9, 2018
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Summary

Magno Humphries Laboratories, Inc. has recalled 2,400 bottles of Senna Laxative (sennosides) tablets, 8.6 mg, because the bottles may actually contain Naproxen Sodium 220 mg tablets instead of the intended laxative. This recall was initiated after a customer complaint confirmed that a bottle labeled as Senna Laxative contained only the pain reliever/fever reducer Naproxen. Taking Naproxen Sodium when intending to take a laxative can lead to unintentional medication errors and potential adverse health effects. These 100-count bottles were manufactured for Basic Drugs, Inc. and distributed nationwide.

Risk

A label mix-up means consumers may unknowingly ingest Naproxen Sodium, a nonsteroidal anti-inflammatory drug (NSAID), which can cause serious side effects such as gastrointestinal bleeding or allergic reactions, especially in individuals with contraindications to NSAIDs.

What You Should Do

  1. Check your medicine cabinet for 100-count bottles of Senna Laxative (sennosides) 8.6 mg with UPC Code 3 07610 22020 1.
  2. Verify if the bottle is from Lot # 352300 with an expiration date of 01/19 (January 2019).
  3. Immediately stop using any tablets from the affected lot, even if they appear to be the correct medication.
  4. Contact your healthcare provider or pharmacist for guidance if you have ingested the wrong medication or have concerns about your health.
  5. Return any unused product to the pharmacy or place of purchase for a full refund.
  6. Contact Magno Humphries Laboratories, Inc. at their Tigard, Oregon facility or your distributor for further instructions regarding this recall.
  7. 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

๐Ÿ’ฐFull Refund

Healthcare 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: Senna Laxative (sennosides) tablets, 8.6 mg (100-count bottles)
Model:
D-0342-2018
UPC Codes:
307610220201
Lot Numbers:
352300 (Exp 01/19)
Date Ranges: Expiration 01/19

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 78952
Status: Resolved
Manufacturer: Magno Humphries Laboratories, Inc
Sold By: Basic Drugs, Inc.
Manufactured In: United States
Units Affected: 2,400 bottles
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.