Recall Atlas
Drugs & medicalClass II

Alchemee, LLC recalls Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%), Packaged as a) 6 fl. oz. (177.4 mL), UPC 7 35786 01528 2; b) 0.33 OZ (9.45g),…

Chemical contamination: Presence of benzene

Read the official notice →
Date
2025-04-16
Country
United States
Brand
Alchemee, LLC
Product
Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%), Packaged as a) 6 fl. oz. (177.4 mL), UPC 7 35786 01528 2; b) 0.33 OZ (9.45g),…
Classification
Class II
Units
Nationwide in the 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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2025-04-16
  2. US
    Drugs & medicalClass I

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: TOL DR R PACK

    Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS: CA, FL, MN, NY, OH, OR, PA, TX, WVOfficial notice →
  3. US
    Drugs & medicalClass I

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CABG OPNHRT S HSP, CARDIAC…

    Medline medical procedure kits, containing Medtronic Aortic Root Cannula

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS: CA, FL, MN, NY, OH, OR, PA, TX, WVOfficial notice →
  4. US
    Drugs & medicalClass II

    Zydus Pharmaceuticals (USA) Inc recalls chlorproMAZINE Hydrochloride Tablets, USP 10 mg, Rx Only, 100 Tablets bottles, Manufactured by: Zydus Lifesciences Ltd., Baddi,…

    CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit

    FDA · DrugZydus Pharmaceuticals (USA) IncNationwide within U.S - MS, AL, TN, VT, OH, ND, MN, WI, SC, AR, FL, IN, LA,…Official notice →
  5. US
    Drugs & medicalClass II

    Somerset Therapeutics Private Limited recalls Haloperidol Decanoate Injection 50mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured by: Somerset Therapeutics Limited,…

    Lack of Assurance of Sterility: Media fill with bacterial contamination

    FDA · DrugSomerset Therapeutics Private LimitedU.S. NationwideOfficial notice →
  6. US
    Drugs & medicalClass II

    B. Braun Medical Inc recalls 0.9% Sodium chloride Irrigation USP, Isotonic Solution for Irrigation, 500 mL Plastic Irrigation Container (PIC), B. Braun Medical, Inc.,…

    Presence of Particulate Matter

    FDA · DrugB. Braun Medical IncProduct was distributed to 12 distributors who may have further distributed…Official notice →
  7. US
    Drugs & medicalClass II

    Glenmark Pharmaceuticals Inc., USA recalls Cetirizine Hydrochloride Tablets, USP, 10mg, 365-count packs, Rx Only, Manufactured for: Glenmark Therapeutics Inc.,…

    CGMP Deviations

    FDA · DrugGlenmark Pharmaceuticals Inc., USAU.S. NationwideOfficial notice →
See all drugs & medical recalls →