Severity
Low
LowClass IIITerminated
FDA Drug recall · Reported April 29, 2015
Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch (NDC 63824-056-72), OTC, Distributed by Reckitt Benckiser, Parsippany, NJ 07054-0224 Made in England
Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch
Reckitt Benckiser LLC recalled Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer t… - a low-severity action.
Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer t… was recalled by Reckitt Benckiser LLC in April 29, 2015. Reason: Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex p…. Check the official notice for the remedy. Verify recall #D-0964-2015 with the FDA Drug before acting.
The recall
Reckitt Benckiser LLC issued this low-severity FDA Drug recall-Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex p….
- Low
- severity level
- Class III
- classification
- April 29, 2015
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0964-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0964-2015) was formally reported on April 29, 2015, with the manufacturer initiating the action on November 10, 2014. It is classified under Low severity (Class III), with a current status of Terminated. Reckitt Benckiser LLC is listed as the recalling firm, operating out of Parsippany, NJ. Federal records list the affected scope as 155 cases (2000 pouches of 2 tablets per case).
The documented reason for this recall is: Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch Distribution data in the federal record shows the product reached: Nationwide. 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, 5 from FDA Drug - 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.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
155 cases (2000 pouches of 2 tablets per case)
Related Recalls
6
5 from same agency
Product description
Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch (NDC 63824-056-72), OTC, Distributed by Reckitt Benckiser, Parsippany, NJ 07054-0224 Made in England
Reason for recall
Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-0964-2015 |
| Date reported | April 29, 2015 |
| Date initiated | November 10, 2014 |
| Recalling firm | Reckitt Benckiser LLC |
| Firm location | Parsippany, NJ |
| Affected scope | 155 cases (2000 pouches of 2 tablets per case) |
| Distribution | Nationwide |
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-0964-2015) 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.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. 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? ▼
Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch (NDC 63824-056-72), OTC, Distributed by Reckitt Benckiser, Parsippany, NJ 07054-0224 Made in England. Recalled by Reckitt Benckiser LLC. Units affected: 155 cases (2000 pouches of 2 tablets per case).
Why was this product recalled? ▼
Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 29, 2015. Severity: Low. Recall number: D-0964-2015.
Where was the recalled product distributed? ▼
Distribution: Nationwide.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0964-2015) 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.
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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 April 29, 2015. 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.