Overview of recall records associated with Glaxosmithkline Consumer Healthcare Holdings, including dates, categories and classifications where available.
Classification mix: Class II: 10, Class III: 3.
Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.
Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.
Labeling: Label lacks warning - Magnesium safety warning is not present on the Gaviscon bottle label.
Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
Fiber prebiotic product potentially contaminated with small plastic pieces
Fiber prebiotic product potentially contaminated with small plastic pieces
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
This page summarizes recall records in which the official source identifies Glaxosmithkline Consumer Healthcare Holdings as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
