Family Dollar Stores, Llc. recalls Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) 24-count Caplets
CGMP deviation: product outside labeled storage temperature requirements.
Read the official notice →- Date
- 2023-05-10
- Country
- United States
- Brand
- Family Dollar Stores
- Product
- Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) 24-count Caplets
- Classification
- Class II
- Units
- Nationwide within the United States
- Category
- Drugs & medical
- Source
- FDA · Drug
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Family Dollar Stores recalls
- 2023-11-15
US
Family Dollar Stores, Llc. recalls MEDIC's CHOICE CONTACT LENS SOLUTION 12FLOZ, SKU 998935
Products were stored outside of labeled temperature requirements.
FDA · DeviceFamily Dollar Stores, Llc.Distributed to Family Dollar stores in the following states: GA, AL, MS, FL,…Official notice →- 2022-09-07
US
Family Dollar Stores, Llc. recalls Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES, Stain Prevention, 5% Hydrogen Peroxide, Net Wt. 2.1 OZ. (59 g) UPC 0…
cGMP deviation: Product held outside of appropriate temperature storage conditions.
FDA · DrugFamily Dollar Stores, Llc.Distributed Nationwide in the USA to the following States: AZ, CA, GA, ID, IN,…Official notice →- 2022-08-31
US
Family Dollar Stores, Llc. recalls QP COUGH COLD TABLET 16 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
CGMP Deviations: product held outside appropriate storage temperature conditions.
- 2022-08-24
US
Family Dollar Stores, Llc. recalls KY JELLY LUBRICANT 2 FL OZ, SKU 901443
Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
FDA · DeviceFamily Dollar Stores, Llc.Product distributed to Family Dollar retail stores in US nationwide.Official notice →- 2022-06-08
US
Family Dollar Stores, Llc. recalls AMBI Skincare Fade Cream Oily Skin New & Improved, Net Wt. 2 OZ (56g)
cGMP deviations: product stored outside of labeled temperature requirements.
Other drugs & medical recalls in the United States
- 2023-05-10
US
Stryker Corporation recalls SafeLight Fiber Optic Cable: Clear, 5MM X 10FT 3.05M, REF: 0233-050-100; Gray, 5MM X 10FT 3.05M, REF: 0233-050-200
Fiber optic cables assembled with not enough epoxy on the proximal end, creating light output issues, which could cause a clinical delay or procedure being converted to open.
FDA · DeviceStryker CorporationWorldwide - US Nationwide distribution including in the states of PA, MS, IL,…Official notice →US
Ottlite TEchnologies, Inc. recalls OttLite Rechargeable UVC Disinfecting Wand
Product allows for the emission of ultraviolet (UV) electronic product radiation in excess of exposure limits recommended by the International Commission on Non-ionizing Radiation Protection (ICNIRP). The emissions are…
US
Gadget Island, Inc recalls DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making…
US
Seatex LLC recalls Seatex Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-Sterile Solution Net Contents: 3.785 L (1 Gallon) Container, UPC 6 12592…
Superpotent Drug and Failed Impurities/Degradation Products: formula does not adhere to the labeled specifications
US
US
Bryant Ranch Prepack, Inc. recalls Lidocaine Patch 5%, 1 patch (63629-8755-20) packaged in 30-count patches per carton (63629-8755-1), Rx only, each patch contains: 700…
Labeling: Typographical error on the upper left-hand side of the box and individual patch label that has the incorrect dosage form stating, each tablet contains instead of each adhesive patch contains.