PlainRecalls
CriticalClass ITerminated

FDA Drug recall · Reported February 21, 2018

Senna Laxative (sennosides) tablets, 8.6 mg, 100-count bottles, Manufactured for: Basic Drugs, Inc., Vandalia, Ohio 45377, UPC Code 3 07610 22020 1.

Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as Senna Laxative contained only tablets of Naproxen Sodium 220 mg.

Recall #
D-0342-2018
Affected scope
2,400 bottles
Initiated
January 17, 2018
Verify with FDA Drug →
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Magno Humphries Laboratories, Inc recalled Senna Laxative (sennosides) tablets, 8.6 mg, 100-count bottles, Manufactured for: Basic D… - a critical-severity action.

Senna Laxative (sennosides) tablets, 8.6 mg, 100-count bottles, Manufactured for: Basic D… was recalled by Magno Humphries Laboratories, Inc in February 21, 2018. Reason: Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as Senna Laxative contained only ta…. Check the official notice for the remedy. Verify recall #D-0342-2018 with the FDA Drug before acting.

The recall

Magno Humphries Laboratories, Inc issued this critical-severity FDA Drug recall-Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as Senna Laxative contained only ta….

Critical
severity level
Class I
classification
February 21, 2018
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-0342-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Drug action (record #D-0342-2018) was formally reported on February 21, 2018, with the manufacturer initiating the action on January 17, 2018. It is classified under Critical severity (Class I), with a current status of Terminated. Magno Humphries Laboratories, Inc is listed as the recalling firm, operating out of Tigard, OR. Federal records list the affected scope as 2,400 bottles.

The documented reason for this recall is: Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as Senna Laxative contained only tablets of Naproxen Sodium 220 mg. Distribution data in the federal record shows the product reached: Nationwide in the USA. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Children & Baby Products recalls over time

Where this recall sits in its category - 3,731 children & baby products recalls on record

0100200300400500600 20052008201120142017202020232026 146
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Critical

Affected scope

2,400 bottles

Related Recalls

6

0 from same agency

Product description

Senna Laxative (sennosides) tablets, 8.6 mg, 100-count bottles, Manufactured for: Basic Drugs, Inc., Vandalia, Ohio 45377, UPC Code 3 07610 22020 1.

Reason for recall

Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as Senna Laxative contained only tablets of Naproxen Sodium 220 mg.

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Critical (Class I)
Status Terminated
Recall number D-0342-2018
Date reported February 21, 2018
Date initiated January 17, 2018
Recalling firm Magno Humphries Laboratories, Inc
Firm location Tigard, OR
Affected scope 2,400 bottles
Distribution Nationwide in the USA

Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (D-0342-2018) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Drug before acting, recall details can be updated.
  • This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next

This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
Senna Laxative (sennosides) tablets, 8.6 mg, 100-count bottles, Manufactured for: Basic Drugs, Inc., Vandalia, Ohio 45377, UPC Code 3 07610 22020 1.. Recalled by Magno Humphries Laboratories, Inc. Units affected: 2,400 bottles.
Why was this product recalled?
Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as Senna Laxative contained only tablets of Naproxen Sodium 220 mg.
Which agency issued this recall?
This recall was issued by the FDA Drug on February 21, 2018. Severity: Critical. Recall number: D-0342-2018.
Where was the recalled product distributed?
Distribution: Nationwide in the USA.
How do I check if my product is affected by a recall?
Check the product description and recall number (D-0342-2018) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nearby Recalls in This Category

Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.

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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported February 21, 2018. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.