Drugs & medicalClass II

Pharma Nobis LLC recalls Fast Acting Earwax Removal System (carbamide peroxide), 6.5%, 0.5 FL OZ (15 mL) Drops per bottle, OTC, Distributed by: CVS Pharmacy, Inc.,…

CGMP Deviations: active ingredient may be subpotent before the labeled expiry due to degradation.

Read the official notice →
Date
2023-04-26
Country
United States
Brand
Pharma Nobis
Product
Fast Acting Earwax Removal System (carbamide peroxide), 6.5%, 0.5 FL OZ (15 mL) Drops per bottle, OTC, Distributed by: CVS Pharmacy, Inc.,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

More Pharma Nobis recalls

  1. 2024-05-22
  2. US
    Drugs & medicalClass II

    Pharma Nobis LLC recalls Meijer Magnesium Citrate Saline Laxative Oral Solution Dye Free, Sugar Free Grape, 10 fl. oz bottle, Distributed by: Meijer Distribution…

    Microbial Contamination of Non-Sterile Products - Presence of Acetobacter nitrogenifigens bacteria

    FDA · DrugPharma Nobis LLCUSA NationwideOfficial notice →
  3. 2024-01-24
  4. US
    Drugs & medicalClass II

    Pharma Nobis LLC recalls Freskaro refresh & revitalize Magnesium Citrate Saline Laxative Oral Solution Grape Flavor 10 fl. oz, Manufactured by: Pharma Lobis, 7400…

    MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.

    FDA · DrugPharma Nobis LLCNationwide.Official notice →
All 3 Pharma Nobis recalls →

Other drugs & medical recalls in the United States

  1. 2023-04-26
  2. US
    Drugs & medicalClass I

    Covidien recalls Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, and Cuffless: Disposable Inner Cannula or Reusable Inner Cannula (REF,…

    A manufacturing error, resulted in a less than specified diameter of adult flexible tracheostomy tube connectors, which results in unsecure connections with 15mm caps and other 15mm circuit components and accessories.…

    FDA · DeviceCovidienWorldwide - US Nationwide distribution including in the states of PR, CA, FL,…Official notice →
  3. US
    Drugs & medicalClass II

    Ascend Laboratories, LLC recalls Aripiprazole Tablets, USP, 20 mg, Rx Only, Packaged in 500-count bottle Manufactured by: Alkem Laboratories Ltd., INDIA Distributed by:…

    Out of specification (OOS) for Spectroscopic Identification test by IR.

    FDA · DrugAscend Laboratories, LLCNationwide in the USAOfficial notice →
  4. US
  5. US
    Drugs & medicalClass II

    Amerisource Health Services LLC recalls Verapamil Hydrochloride Extended-Release Tablets, USP, 180 mg, 100 Tablets (10 x 10) per carton, Rx only, Distributed by:…

    Failed Dissolution Specifications: Out of specification dissolution results above specified values.

    FDA · DrugAmerisource Health Services LLCNationwide in the USAOfficial notice →
  6. 2023-04-19
  7. US
    Drugs & medicalClass II

    Covidien, LP recalls Step Bladeless Trocars, 10 mm cannula and dilator with radially expandable sleeve and 5 - 10 mm reducer, Product Number S101010

    Medtronic was made aware of a supplier calibration issue during the contract sterilization process that may lead to unsterile product. Use of affected product may lead to an unspecified infection or, in the case of…

    FDA · DeviceCovidien, LPWorldwide Distribution: US (nationwide) to States of: AR, CA, FL, GA, LA, MA,…Official notice →
  8. US
    Drugs & medicalClass II

    Howmedica Osteonics Corp. recalls stryker MAKO RESTORIS MCK BASEPLATE TRIAL (SIZE 6 RM/LL), REF 170616, intended for use in a Partial Knee Arthroplasty surgical procedure

    Certain lots of the Restoris MultiCompartmental Knee (MCK) Tibial Baseplate Trials contain product with incorrect size laser marking

    FDA · DeviceHowmedica Osteonics Corp.U.S., Netherlands, Japan, China, India, Korea, and Australia.Official notice →
See all drugs & medical recalls →