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

Read the official notice →
Date
2025-01-29
Country
United States
Brand
First Aid Beauty Ltd
Product
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,…
Classification
Class II
Units
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 Details may be shortened or out of date; the official notice is the authoritative source.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

  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.

Other drugs & medical recalls in the United States

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

    Jinan Bodor Cnc Machine Co Ltd recalls Bodor P and C series laser cutting machines

    Non-compliant laser products

    FDA · DeviceJinan Bodor Cnc Machine Co LtdUS Nationwide DistributionOfficial notice →
  3. 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 →
  4. 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 →
  5. US
    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.

    FDA · DrugBrands International CorporationNationwide USAOfficial notice →
  6. 2025-01-22
  7. 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 →
  8. 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 →
See all drugs & medical recalls →