Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

Home
/
Brands
/
GlaxoSmithkline Consmer Healthcare

GlaxoSmithkline Consmer Healthcare Recalls

All product recalls associated with GlaxoSmithkline Consmer Healthcare.

Get alerts for this brand

Recall Summary

Total Recalls

68

Past Year

0

Class I (Serious)

3

Most Recent

May 2024

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 41–60 of 68 recalls

Sensodyne Extra Fresh (GlaxoSmithKline) – Foreign Substance (2015)

Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.

Class IIModerate

FDAJul 15, 2015Nationwide• GlaxoSmithkline Consmer Healthcare

Biotene Fluoride Toothpaste (GlaxoSmithKline) – wood fragments (2015)

Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.

Class IIModerate

FDAJul 15, 2015Nationwide• GlaxoSmithkline Consmer Healthcare

Biotene Fresh Mint Toothpaste (GlaxoSmithKline) – wood fragments (2015)

Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.

Page 3 of 4Next

Class IIModerate

FDAJul 15, 2015Nationwide• GlaxoSmithkline Consmer Healthcare

Sensodyne Extra Fresh (GlaxoSmithKline) – wood fragments (2015)

Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.

Class IIModerate

FDAJul 15, 2015Nationwide• GlaxoSmithkline Consmer Healthcare

Panadol Extra Strength (GlaxoSmithKline) – dissolution failure (2015)

Failed Dissolution Specifications

FDAJun 30, 2015PR• GlaxoSmithkline Consmer Healthcare

Panadol Advance (GSK) – Closure Failure (2014)

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

CPSCJul 14, 2014Nationwide• GlaxoSmithKline (GSK), of Moon Township, Penn.

Nicorette Lozenges Mini (GlaxoSmithKline) – Specification Failure (2014)

Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.

FDAFeb 20, 2014Nationwide• GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Nicotine Polacrilex Lozenge 4mg (GlaxoSmithKline) – Specification Failure (2014)

Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.

FDAFeb 20, 2014Nationwide• GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Nicorette & NicoDerm CQ (GlaxoSmithKline) – Specification Failure (2014)

Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.

FDAFeb 20, 2014Nationwide• GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Nicotine Polacrilex Lozenge 2mg (GlaxoSmithKline) – Specification Failure (2014)

Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.

FDAFeb 20, 2014Nationwide• GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Nicorette Product Line (GlaxoSmithKline) – Specification Failure (2014)

Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.

FDAFeb 20, 2014Nationwide• GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

2006 SKYLINE SKYCAT Recall: LATCHES/LOCKS/LINKAGES

Skyline Corporation (Skyline) is recalling certain model year 2006-2013 recreational vehicle travel trailers and fifth-wheel trailers manufactured January 1, 2006, through May, 31, 2013 and equipped with Fastec-brand door locks. It may be possible to remove the key from the lock in a way that potentially jams the deadbolt.

NHTSADec 9, 2013Nationwide• SKYLINE

Sumatriptan Succinate Injection (GlaxoSmithKline) – sterility concern (2013)

Lack of Assurance of Sterility: A small number of pre-filled syringes may contain needles which protrude through the needle shield.

Class IIModerate

FDANov 6, 2013Nationwide• GlaxoSmithKline, LLC.

Imitrex STATdose System (GlaxoSmithKline) – needle shield issue (2013)

Lack of Assurance of Sterility: A small number of pre-filled syringes may contain needles which protrude through the needle shield.

Class IIModerate

FDANov 6, 2013Nationwide• GlaxoSmithKline, LLC.

KEYLINE TRAILER DOOR Equipment Recall: EQUIPMENT

Keyline Sales is recalling certain exterior doors manufactured January 1, 2006, through April 25, 2013 for use in cargo and specialty trailers that were built with Fastec-brand door locks. It may be possible to remove the key from the lock in a way that potentially jams the deadbolt.

NHTSAOct 17, 2013Nationwide• KEYLINE

TUMS Ultra (GlaxoSmithKline) – Foreign Tablets (2013)

Presence of Foreign Tablets/Capsules: Product labeled TUMS Ultra Assorted Berries 1000mg Chewable tables, may contain EX TUMS Assorted Berries 750mg tablets

FDAJul 18, 2013Nationwide• GlaxoSmithKline, LLC.

Advair HFA Inhaler (GlaxoSmithKline) – Particle Distribution Issue (2012)

Product Lacks Stability: These lots are being recalled due to the failure to meet the particle size distribution specification.

FDAOct 24, 2012Nationwide• GlaxoSmithKline, LLC.

Advair HFA Inhaler (GlaxoSmithKline) – Particle Distribution Issue (2012)

Product Lacks Stability: These lots are being recalled due to the failure to meet the particle size distribution specification.

FDAOct 24, 2012Nationwide• GlaxoSmithKline, LLC.

Arranon Injection (GlaxoSmithKline) – Impurity Concerns (2012)

Impurities/Degradation Products: Potential for drug related impurities to exceed the specification limits.

Class IIModerate

FDAOct 8, 2012Nationwide• GlaxoSmithKline, LLC.

Ventolin HFA Inhaler (GlaxoSmithKline) – Improper Dose (2012)

Does Not Deliver Proper Metered Dose: Potential content of albuterol per dose is below specification.

Class IIModerate

FDAJul 26, 2012Nationwide• GlaxoSmithKline Inc