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.
Read the official notice →- Date
- 2022-06-08
- Country
- United States
- Brand
- Family Dollar Stores
- Product
- AMBI Skincare Fade Cream Oily Skin New & Improved, Net Wt. 2 OZ (56g)
- Classification
- Class II
- Units
- USA Nationwide
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
USFamily 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 →- 2023-05-10
- US
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.
- 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 →
Other drugs & medical recalls in the United States
- 2022-06-08
- US
Baxter Healthcare Corporation recalls 3,65 m Extension Set with Luer-lock Connector
Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.
FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the states of CA, MO, MA, AZ, TX, FL, NY, MD, OH.Official notice → - US
Baxter Healthcare Corporation recalls In-Line ventilator adaptor
There is a potential of reduced oxygenation or pneumothorax/barotrauma to occur when the Volara system is used with in-line ventilator in home care environment.
FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the states of TX, FL, VA, KY, CA, AZ, WI, IL,…Official notice → - US
Teva Pharmaceuticals USA Inc recalls Anagrelide Capsules USP, 0.5 mg, 100-count bottles, Rx Only, Manufactured in India For: TEVA PHARMACEUTICALS USA, Inc., North…
Failed Dissolution Specifications- Low Out-Of-Specification results obtained during stability testing.
- US
Strides Pharma Inc. recalls Losartan Potassium Tablets, USP, 50 mg, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No., 101, 102, 107 & 108,…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- US
Direct Rx recalls Losartan Pot./HCTZ 100/12.5 mg Packaged and Distributed By: Direct Rx Dawsonville, GA 30534 Mfg For: Lupin Pharmaceuticals, Inc.…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- US
Vi-Jon, LLC recalls Equate Tartar Control Plus (Eucalyptol 0.092%, Menthol 0.042%, Methyl salicylate 0.060%, Thymol 0.064%) Antiseptic Mouthrise Plus,…
Superpotent Drug: product complaint for milky blue appearance and consistency, further investigation by the firm found the recalled lots out of specification for the four active ingredients.