Severity
Low
LowClass IIITerminated
FDA Drug recall · Reported August 12, 2015
Panadol (acetaminophen) Extra Strength, 500 mg, a) 30 count (UPC 1-03-53100-91070-8, NDC 0135-0135-02), b) 60 count (UPC 1-03-53100-91080-7, NDC 0135-0135-03) and c) 100 count (UPC 1-03-53100-91090-6, NDC 0135-0135-04) bottles, Distributed by: GlaxoSmithKline Consumer Healthcare L.P, Moon Township, PA 15108
Failed Dissolution Specifications
GlaxoSmithkline Consmer Healthcare recalled Panadol (acetaminophen) Extra Strength, 500 mg, a) 30 count (UPC 1-03-53100-91070-8, NDC … - a low-severity action.
Panadol (acetaminophen) Extra Strength, 500 mg, a) 30 count (UPC 1-03-53100-91070-8, NDC … was recalled by GlaxoSmithkline Consmer Healthcare in August 12, 2015. Reason: Failed Dissolution Specifications. Check the official notice for the remedy. Verify recall #D-1287-2015 with the FDA Drug before acting.
The recall
GlaxoSmithkline Consmer Healthcare issued this low-severity FDA Drug recall-Failed Dissolution Specifications.
- Low
- severity level
- Class III
- classification
- August 12, 2015
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-1287-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-1287-2015) was formally reported on August 12, 2015, with the manufacturer initiating the action on June 30, 2015. It is classified under Low severity (Class III), with a current status of Terminated. GlaxoSmithkline Consmer Healthcare is listed as the recalling firm, operating out of Moon Township, PA. Federal records list the affected scope as 17,675 cases.
The documented reason for this recall is: Failed Dissolution Specifications Distribution data in the federal record shows the product reached: Puerto Rico and Virgin Islands. 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
17,675 cases
Related Recalls
6
5 from same agency
Product description
Panadol (acetaminophen) Extra Strength, 500 mg, a) 30 count (UPC 1-03-53100-91070-8, NDC 0135-0135-02), b) 60 count (UPC 1-03-53100-91080-7, NDC 0135-0135-03) and c) 100 count (UPC 1-03-53100-91090-6, NDC 0135-0135-04) bottles, Distributed by: GlaxoSmithKline Consumer Healthcare L.P, Moon Township, PA 15108
Reason for recall
Failed Dissolution Specifications
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-1287-2015 |
| Date reported | August 12, 2015 |
| Date initiated | June 30, 2015 |
| Recalling firm | GlaxoSmithkline Consmer Healthcare |
| Firm location | Moon Township, PA |
| Affected scope | 17,675 cases |
| Distribution | Puerto Rico and Virgin Islands |
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-1287-2015) 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? ▼
Panadol (acetaminophen) Extra Strength, 500 mg, a) 30 count (UPC 1-03-53100-91070-8, NDC 0135-0135-02), b) 60 count (UPC 1-03-53100-91080-7, NDC 0135-0135-03) and c) 100 count (UPC 1-03-53100-91090-6, NDC 0135-0135-04) bottles, Distributed by: GlaxoSmithKline Consumer Healthcare L.P, Moon Township, PA 15108. Recalled by GlaxoSmithkline Consmer Healthcare. Units affected: 17,675 cases.
Why was this product recalled? ▼
Failed Dissolution Specifications
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 12, 2015. Severity: Low. Recall number: D-1287-2015.
Where was the recalled product distributed? ▼
Distribution: Puerto Rico and Virgin Islands.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-1287-2015) 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.
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 August 12, 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.