Drugs & medicalClass II

Brands International Corporation recalls Kissable Diabetics Foot Cream, NET WT 4 oz (113 g) per tube, Manufactured By: Brands International Corp., Newmarket, ON, L3X…

CGMP Deviations: lack of adequate release testing.

Read the official notice →
Date
2025-01-29
Country
United States
Brand
Brands
Product
Kissable Diabetics Foot Cream, NET WT 4 oz (113 g) per tube, Manufactured By: Brands International Corp., Newmarket, ON, L3X 2S2. UPC 6…
Classification
Class II
Units
Nationwide USA
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 Details may be shortened or out of date; the official notice is the authoritative source.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

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. 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 Brands recalls

  1. 2024-07-24
  2. US
    Drugs & medicalClass II

    Brands International Corporation recalls Oatmeal Daily Moisturizing Body Lotion (1.3% Dimethicone), 8 fl oz (236mL), packaged in an HDPE bottle 12 bottles per case,…

    Microbial Contamination of Non-Sterile Products: confirmed presence of mold contamination

    FDA · DrugBrands International CorporationUSA nationwide.Official notice →
All 2 Brands recalls →

Other drugs & medical recalls in the United States

  1. 2025-01-29
  2. US
    Drugs & medicalClass III

    Appco Pharma LLC recalls Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598-943-90.

    Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet

    FDA · DrugAppco Pharma LLCNationwide USA.Official notice →
  3. US
    Drugs & medicalClass I

    SHOPPERS- PLAZA recalls FOUZEE SugarLin HERBAL FORMULA capsules, 180 capsules per bottle, Sold and Distributed by Shoppers-Plaza, Hawthorne, CA 90250. Product of…

    Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed product tainted with undeclared metformin and glyburide

    FDA · DrugSHOPPERS- PLAZANationwide via internet salesOfficial notice →
  4. US
    Drugs & medicalClass II

    First Aid Beauty Ltd recalls First Aid Beauty Ultra Repair Cream, colloidal oatmeal 0.5%, Coconut Vanilla, Net Wt. 396.8 g (14 OZ), DISTR. BY: First Aid Beauty LTD,…

    CGMP Deviations; product intended for quarantine was inadvertently distributed

    FDA · DrugFirst Aid Beauty LtdNationwideOfficial notice →
  5. 2025-01-22
  6. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls LithoCrushV Single Use Mechanical Lithotriptor V. Model Number: BML-V442QR-30. Single Use Mechanical Lithotriptor V used…

    Potential for distal tip tearing of the Mechanical Lithotriptor V.

    FDA · DeviceOlympus Corporation of the AmericasUS Nationwide distribution.Official notice →
  7. US
    Drugs & medicalClass II

    Accriva Diagnostics, Inc. recalls VerifyNow P2Y12 Platelet Reactivity Test, REF: 85064

    Platelet Reactivity Test distributed without appropriate US-FDA market clearance; if used healthcare personnel could use the baseline PRUTest measurement prior to initiating drug therapy, and then use the percent…

    FDA · DeviceAccriva Diagnostics, Inc.US Nationwide distribution in the state of VA.Official notice →
  8. US
    Drugs & medicalClass II

    A L I Technologies Ltd recalls Change Healthcare Cardiology Hemo software

    Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).

    FDA · DeviceA L I Technologies LtdUS Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO,…Official notice →
See all drugs & medical recalls →