Class II · Moderate risk Ongoing
Children's Ibuprofen Oral Suspension
Reason Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product.
Ibuprofen 200 mg liquid filled capsules Advil Liqui-Gel Minis
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
What was recalled
Ibuprofen 200 mg liquid filled capsules Advil Liqui-Gel Minis, 160 count bottle NDC 0573-1769-89 NDC 0573-1769-95
- Recalling firm
- Glaxosmithkline Consumer Healthcare Holdings
- NDC code
- 0573-1769-89
- Origin
- NJ, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1066-2020
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Ibuprofen recalls
See all
Class II · Moderate risk Ongoing
Advil a) Ibuprofen
Reason CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Class II · Moderate risk Ongoing
Acetaminophen and Ibuprofen
Reason CGMP Deviations
Class III · Low risk Ongoing
IBU (ibuprofen) 600 mg tablets, 500-count bottle, Rx Only…
Reason Failed Tablet/Capsule Specifications
Class II · Moderate risk Ongoing
Ibuprofen 800mg
Reason Failed Impurities/Degradation Specifications: Product failed impurity specifications at the 18-month stability testing.
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