Recall Atlas
Drugs & medicalClass II

Ecometics, Inc. recalls Unguentine Original Maximum Strength Pain Relieving/Antiseptic Ointment (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Oxide 6.6%),…

CGMP DEVIATIONS

Read the official notice →
Date
2023-03-15
Country
United States
Brand
Ecometics
Product
Unguentine Original Maximum Strength Pain Relieving/Antiseptic Ointment (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Oxide 6.6%),…
Classification
Class II
Units
Nationwide within the United States
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Ecometics recalls

  1. 2023-08-30
  2. US
    Drugs & medicalClass II

    Ecometics, Inc. recalls activator concentrate, Sodium Fluoride 0.96% in Activator Concentrate; 0.08% in diluted Activator Solution, Net 1 FL. OZ., Manufactured…

    CGMP Deviations: Products not manufactured under current good manufacturing practices.

    FDA · DrugEcometics, Inc.Nationwide in the USAOfficial notice →
All 2 Ecometics recalls →

Other drugs & medical recalls in the United States

  1. 2023-03-15
  2. US
    Drugs & medicalClass I

    Pharmedica USA, LLC recalls Purely Soothing 15% MSM Drops, packaged in a)15 ml, .5 fl oz bottle, UPC 7 31034 91382 9; and b) 30 ml, 1.014 fl oz bottle, UPC 7 31034…

    Non-Sterility

    FDA · DrugPharmedica USA, LLCNationwide in the USA and Worldwide through e-commerce and trade showsOfficial notice →
  3. US
    Drugs & medicalClass I

    Nanomaterials Discovery Corporation recalls Snowy Range Blue Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-Sterile Solution, 4fl. oz. [118mL], Distributed…

    Chemical Contamination: FDA analysis found the product to contain methanol, acetaldehyde, and acetal above the limits.

    FDA · DrugNanomaterials Discovery CorporationNationwide in the USAOfficial notice →
  4. US
    Drugs & medicalClass III

    Akron Pharma, Inc. recalls DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-2829-1

    Labeling: Incorrect or Missing Lot and/or Exp Date

    FDA · DrugAkron Pharma, Inc.Nationwide within the United StatesOfficial notice →
  5. US
    Drugs & medicalClass II

    Denver Solutions, LLC DBA Leiters Health recalls Phenylephrine HCl 40 mg (160 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV Bag, Leiter Compounding Health 13796…

    CGMP DEVIATIONS

    FDA · DrugDenver Solutions, LLC DBA Leiters HealthNationwide within the United States including VA or other Government facilitiesOfficial notice →
  6. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA Inc recalls Metformin hydrochloride Extended-Release Tablets, 1000 mg, 60-count bottle, RX only, Manufactured by: Actavis Laboratories FL,…

    CGMP Deviations: Detection of N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit.

    FDA · DrugTeva Pharmaceuticals USA IncCAOfficial notice →
  7. US
    Drugs & medicalClass II

    Nutraceutical Corporation recalls NaturalCare bioAllers, Mold, Yeast and Dust, Homeopathic, Liquid Drops, 20% Alcohol, 1 FL OZ( 30mL), Mfd. for Nutraceutical Corp.…

    CGMP Deviations: Raw material recalled by repackager, due to discoloration.

    FDA · DrugNutraceutical CorporationNationwide in the USA.Official notice →
See all drugs & medical recalls →