Drugs & medicalClass I

Jarman's Midwest Cleaning Systems, Inc. recalls SOFT HANDS Alcohol Antiseptic 80%, Topical Solution, HAND SANITIZER, NON-STERILE SOLUTION, cleanpro SUPPLY, 1 US gallon…

Chemical Contamination: FDA testing found Presence of methanol

Read the official notice →
Date
2023-06-21
Country
United States
Brand
Jarman's Midwest Cleaning Systems
Product
SOFT HANDS Alcohol Antiseptic 80%, Topical Solution, HAND SANITIZER, NON-STERILE SOLUTION, cleanpro SUPPLY, 1 US gallon / 3785.41ml,…
Classification
Class I
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Jarman's Midwest Cleaning Systems recalls

  1. 2023-06-21
  2. US
    Drugs & medicalClass II

    Jarman's Midwest Cleaning Systems, Inc. recalls Isopropyl Alcohol Antiseptic 75%, Topical Solution, Hand Sanitizer Non-sterile Solution, Volume: 3.785 L, plastic gallon…

    CGMP deficiencies: Product manufactured at the same site where FDA testing found Presence of methanol in other products.

    FDA · DrugJarman's Midwest Cleaning Systems, Inc.Nationwide in the USAOfficial notice →
All 2 Jarman's Midwest Cleaning Systems recalls →

Other drugs & medical recalls in the United States

  1. 2023-06-21
  2. US
    Drugs & medicalClass I

    NOXBOX LTD recalls NOxBOXi Nitric Oxide Delivery System, NOXBOX-I, REQNOXBOX-I, Nitric Oxide Delivery Device

    Device may experience malfunctions due to misalignment of the check valve in the manifold. If the device fails, there is a risk of nitric oxide leak, oxygen gas leak, or earlier cylinder gas changeover than expected or…

    FDA · DeviceNOXBOX LTDWorldwide distribution - US Nationwide and the countries of Bahrain, Bolivia,…Official notice →
  3. US
    Drugs & medicalClass II

    Amneal Pharmaceuticals of New York, LLC recalls Extended Phenytoin Sodium Capsules, USP, 100 mg, Rx Only, 100 capsules per bottle, Distributed by: Amneal…

    Failed Dissolution Specifications: Out-of-specification results for dissolution (above specification)

    FDA · DrugAmneal Pharmaceuticals of New York, LLCLA, PA and OH.Official notice →
  4. US
    Drugs & medicalClass III

    AVKARE LLC recalls Tranexamic Acid USP Tablets, 650 mg, 30 tablets (3X10) Unit Dose, Rx Only, Manufactured for: AvKARE Pulaski, TN 38478, NDC 50268-772-13

    Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.

    FDA · DrugAVKARE LLCNationwide in the USA.Official notice →
  5. US
    Drugs & medicalClass II

    Jarman's Midwest Cleaning Systems, Inc. recalls Isopropyl Alcohol Antiseptic 75%, Topical Solution, Hand Sanitizer Non-sterile Solution, Volume: 3.785 L, plastic gallon…

    CGMP deficiencies: Product manufactured at the same site where FDA testing found Presence of methanol in other products.

    FDA · DrugJarman's Midwest Cleaning Systems, Inc.Nationwide in the USAOfficial notice →
  6. US
    Drugs & medicalClass III

    Amring Pharmaceuticals Inc recalls Lysteda (tranexamic acid) USP Tablets, 650 mg, 30 tablets per bottle, Rx Only, Manufactured for: Amring Pharmaceuticals Inc. Berwyn,…

    Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.

    FDA · DrugAmring Pharmaceuticals IncNationwide in the USA.Official notice →
  7. 2023-06-14
  8. US
    Drugs & medicalClass II

    C.R. Bard Inc recalls HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e) REF 71816, f) REF…

    Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.

    FDA · DeviceC.R. Bard IncWorldwideOfficial notice →
See all drugs & medical recalls →