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CPSC recall · Reported July 14, 2014

GSK Recalls Panadol Advance Bottles Due to Failure to Meet Child-Resistant Closure Requirement; Sold Exclusively in Puerto Rico

The packaging is not child-resistant as required by the Poison Prevention Packaging Act. These products contain acetaminophen which is required by the Poison Prevention Packaging …

Recall #
14229
Affected scope
About 10,600
Verify with CPSC →
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GlaxoSmithKline (Gsk), of Moon Township, Penn. recalled This recall involves bottles of 100ct Panadol Advance pain relievers. The medicine was so….

GSK Recalls Panadol Advance Bottles Due to Failure to Meet Child-Resistant Closure Requir… was recalled by GlaxoSmithKline (Gsk), of Moon Township, Penn. in July 14, 2014. Reason: The packaging is not child-resistant as required by the Poison Prevention Packaging Act. These products conta…. Remedy: Consumers should immediately place the product out of a child's sight and reach, and cont…. Verify recall #14229 with the CPSC before acting.

The recall

GlaxoSmithKline (Gsk), of Moon Township, Penn. issued this CPSC recall-The packaging is not child-resistant as required by the Poison Prevention Packaging Act. These products conta….

None
agency class
July 14, 2014
reported

Sourced from official CPSC enforcement records. Verify recall #14229 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. Consumers holding this product should act on the agency's documented remedy above rather than relying on general guidance.

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.

Drugs & Medications recalls over time

Where this recall sits in its category - 14,472 drugs & medications recalls on record

05001,0001,5002,000 2006201220152018202120242026 448

Product description

This recall involves bottles of 100ct Panadol Advance pain relievers. The medicine was sold in white containers with a blue label, inside a blue box. "Panadol" and "Advance" are printed on the label. Lot numbers and dates codes are located on the left side panel of the box and on the left side of the label on the bottle, near the bar code. Lot numbers and date codes included in the recall are: Lot number: 14241, expiration date: 02/2015 Lot number: 14002, expiration date: 10/2014 Lot number: 13881, expiration date: 09/2014 Lot number: 13801, expiration date: 09/2014

Reason for recall

The packaging is not child-resistant as required by the Poison Prevention Packaging Act. These products contain acetaminophen which is required by the Poison Prevention Packaging Act to be sealed with child-resistant packaging.

Remedy, what to do

Consumers should immediately place the product out of a child's sight and reach, and contact GSK for a refund.

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Not classified by agency
Status Active
Recall number 14229
Date reported July 14, 2014
Date initiated July 14, 2014
Recalling firm GlaxoSmithKline (Gsk), of Moon Township, Penn.
Affected scope About 10,600
Distribution Not disclosed
Official source CPSC notice →

Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.

What to do with this recall

Consumers should immediately place the product out of a child's sight and reach, and contact GSK for a refund.

  • Check the recall number (14229) and product description against the item you own. Search the archive
  • Confirm the current status and remedy on the official CPSC notice before acting. CPSC notice
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official CPSC 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?
This recall involves bottles of 100ct Panadol Advance pain relievers. The medicine was sold in white containers with a blue label, inside a blue box. "Panadol" and "Advance" are printed on the label. Lot numbers and dates codes are located on the left side panel of the box and on the left side of the label on the bottle, near the bar code. Lot numbers and date codes included in the recall are: Lot number: 14241, expiration date: 02/2015 Lot number: 14002, expiration date: 10/2014 Lot number: 13881, expiration date: 09/2014 Lot number: 13801, expiration date: 09/2014. Recalled by GlaxoSmithKline (Gsk), of Moon Township, Penn.. Units affected: About 10,600.
Why was this product recalled?
The packaging is not child-resistant as required by the Poison Prevention Packaging Act. These products contain acetaminophen which is required by the Poison Prevention Packaging Act to be sealed with child-resistant packaging.
What should consumers do?
Consumers should immediately place the product out of a child's sight and reach, and contact GSK for a refund.
Which agency issued this recall?
This recall was issued by the CPSC on July 14, 2014. CPSC does not publish a hazard classification for this recall. Recall number: 14229.
How do I report an injury from a recalled product?
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.

Nationwide recalls with similar severity or category timing

Consumer-product notices outside this firm and state, matched by severity timing and product category.

Compare this recall with Kian Pee Wan Capsules, 30-count bottles → · All Drugs & Medications recalls

This recall: CPSC, reported July 14, 2014. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026