CLASS II ONGOING Drug recall · Reported 10 May 2023 · FDA Enforcement Report
Advil Liqui-Gels Solubilized Ibuprofen Capsules recalled
Family Dollar Stores is recalling Advil Liqui-Gels Solubilized Ibuprofen Capsules, 200 mg Pain Reliever/Fever Reducer, distributed nationwide in the US. The recall was initiated on 31 Mar 2023 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0566-2023
- FDA event ID
- 92248
- Recalling firm
- Family Dollar Stores, Chesapeake, VA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 31 Mar 2023
- FDA classified
- 4 May 2023
- Reported
- 10 May 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Manufacturing (CGMP) Deviations
- Drug class
- Pain Medication
Timeline
| 31 Mar 2023 | Recall initiated by company | |
| 4 May 2023 | Classified by FDA | +34 days |
| 10 May 2023 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP deviation: product outside labeled storage temperature requirements.
Product as listed by the FDA
Advil Liqui-Gels Solubilized Ibuprofen Capsules, 200 mg Pain Reliever/Fever Reducer (NSAID) a) 20-count Liquid Filled Capsule bottles; b) 40-count Liquid Filled Capsule bottles.
Where it was distributed
Nationwide within the United States
Stores named: Dollar Tree
Questions about this recall
Why was it recalled?
CGMP deviation: product outside labeled storage temperature requirements.
Which lots are affected?
SKUs a) 0999841; b) 0916071 stored and distributed from DCs 07/28/2022 through 03/31/2023.
Where was it sold?
Nationwide within the United States
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
3 other products · FDA event 92248This product is part of a recall event; the main page for the event is Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer recalled | Family Dollar Stores | Manufacturing (CGMP) Deviations | Nationwide | |
| CLASS II | Advil Dual Action with Acetaminophen 250 mg and Ibuprofen recalled | Family Dollar Stores | Manufacturing (CGMP) Deviations | Nationwide | |
| CLASS II | Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (Nsaid) recalled | Family Dollar Stores | Manufacturing (CGMP) Deviations | Nationwide |
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|---|---|---|---|---|---|
| Device | CLASS II | Veriquick Pregnancy Test recalled by Family Dollar Stores | Family Dollar Stores | Temperature Abuse | 23 states |
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| Device | CLASS II | At Home Marijuana Test Strip recalled by Family Dollar Stores | Family Dollar Stores | Temperature Abuse | 23 states |
| Device | CLASS II | Goodsense Denture Cleanser Grn Tab recalled by Family Dollar Stores | Family Dollar Stores | Temperature Abuse | 23 states |