This recall has not yet been classified by risk level.
GSK Recalls Panadol Advance Bottles Due to Failure to Meet Child-Resistant Closure Requirement; Sold Exclusively in Puerto Rico
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Consumers should immediately place the product out of a child's sight and reach, and contact GSK for a refund. Options: Refund
Affected Products
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
Why Was This 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.
Where Was This Sold?
Distribution information not available.
About GlaxoSmithKline (GSK), of Moon Township, Penn.
GlaxoSmithKline (GSK), of Moon Township, Penn. has 1 total recall tracked by RecallDetector.
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Data sourced from the CPSC. Last updated March 26, 2026. View original report