Drugs & medicalClass II

Consumer Product Partners, LLC recalls Petroleum Jelly, White Petrolatum USP, NET WT 13 OZ (368g), sold under the following brands - Rite Aid, with UPC 0-11822-51349-4;…

Labeling: Label Mix up; product labeled as pure white petroleum jelly actually contains petroleum jelly with Lavendar and Chamomile

Read the official notice →
Date
2024-06-26
Country
United States
Brand
Consumer Product Partners
Product
Petroleum Jelly, White Petrolatum USP, NET WT 13 OZ (368g), sold under the following brands - Rite Aid, with UPC 0-11822-51349-4; Kroger,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

More Consumer Product Partners recalls

  1. 2025-10-01
  2. US
  3. 2025-06-11
  4. US
    Drugs & medicalClass II

    Consumer Product Partners, LLC recalls Spectrum Advanced Gel Hand Sanitizer, Ethyl alcohol 70%, 8 FL OZ (236 mL) per bottle, Manufactured for Medline Industries, Inc.,…

    Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol

    FDA · DrugConsumer Product Partners, LLCNationwide in the USA.Official notice →
  5. 2025-04-02
  6. US
    Drugs & medicalClass II

    Consumer Product Partners, LLC recalls [CORRECT FRONT PANEL] Hydrogen Peroxide Topical Solution, USP, 32 FL OZ (1 QT) 946 mL per bottle, NDC 0869-0871-45; [INCORRECT…

    Labeling; Label Mixup; some bottles have an incorrect back label indicating 91% Isopropyl Alcohol

    FDA · DrugConsumer Product Partners, LLCVAOfficial notice →
All 4 Consumer Product Partners recalls →

Other drugs & medical recalls in the United States

  1. 2024-06-26
  2. US
    Drugs & medicalClass I

    Hamilton Medical AG recalls Ventilator HAMILTON-C6, PN: 160021

    Ventilator may enter sensor fail mode, ventilation may not re-initiate, after patient is reconnected, which may cause hypoxia, if this sequence occurs: 1)User presses O2 enrichment, 2)User disconnects endotracheal tube…

    FDA · DeviceHamilton Medical AGUS Nationwide distribution in the states of GA, KY, FL, IN, NV, MI, VA, OR,…Official notice →
  3. US
    Drugs & medicalClass II

    Breckenridge Pharmaceutical, Inc recalls Duloxetine Delayed-Release Capsules, USP, 60mg, 90-count bottle, Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles,…

    CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit

    FDA · DrugBreckenridge Pharmaceutical, IncNationwide in the USAOfficial notice →
  4. US
  5. US
  6. US
    Drugs & medicalClass II

    MexHealth LLC recalls OSSOS-SANS Reforzado con: Glucosamina Curcuma Ortiga tablets, packaged in a 30-count bottle, DISTRIBUIDOR POR: Naturistas Especializados,…

    Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac and methocarbamol,

    FDA · DrugMexHealth LLCUS NationwideOfficial notice →
  7. US
    Drugs & medicalClass II

    Denison Pharmaceuticals, LLC recalls Little Remedies Gas Relief Drops (Simethicone/Antigas), packaged in 1 fl. oz. (30 mL) bottle with dropper, Dist by Medtech Products…

    cGMP deviations: Test results confirmed aypical Burkholderia Cepacia were a result of personnel error.

    FDA · DrugDenison Pharmaceuticals, LLCRecalled units were distributed to one customer. 100% recovered (113,544…Official notice →
See all drugs & medical recalls →