Drugs & medicalClass II

Lula Holdings L.L.C. recalls Kill 'Dat Sanitizing Products Hand Sanitizer, 1 gallon (128 fl. oz.) 80% Alcohol, OTC, Manufactured by: Lula Holdings LLC, 15532 St.…

CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits.

Read the official notice →
Date
2022-05-18
Country
United States
Brand
Lula Holdings L.L.C.
Product
Kill 'Dat Sanitizing Products Hand Sanitizer, 1 gallon (128 fl. oz.) 80% Alcohol, OTC, Manufactured by: Lula Holdings LLC, 15532 St.…
Classification
Class II
Units
LA
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2022-05-18
  2. US
    Drugs & medicalClass I

    MESA BIOTECH, INC recalls Accula SARS-CoV-2 Test, REF: COV4100

    SARS-CoV-2 Test has an increased potential for false positive results, which may lead to a delay in correct diagnosis and treatment.

    FDA · DeviceMESA BIOTECH, INCUS Nationwide distribution in the states of CA, TX, MA, NY, FL, NC, NJ, GA,…Official notice →
  3. US
  4. US
    Drugs & medicalClass II

    Mylan Institutional, Inc. (d.b.a. UDL Laboratories) recalls Esomeprazole Magnesium Delayed-Release Capsules, USP 20 mg, packaged in Unit Dose Blister Cards of 6 (10…

    Failed Impurities/Degradation Specifications: OOS result was obtained for Any Other Individual Impurity at the 12M room temperature time point.

    FDA · DrugMylan Institutional, Inc. (d.b.a. UDL Laboratories)Nationwide within USAOfficial notice →
  5. US
    Drugs & medicalClass III

    SUN PHARMACEUTICAL INDUSTRIES INC recalls buPROPion Hydrochloride Extended-Release Tablet, USP (SR), 200 mg, 60-count bottle, Rx only Distributed by: Sun Pharmaceutical…

    Presence Of Foreign Substance: Customer complaint for the presence of dark, gritty substance found within the bottle which was determined to be activated carbon from the desiccant canister inside the bottle.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide in the USAOfficial notice →
  6. US
    Drugs & medicalClass I

    Fagron, Inc recalls SyrSpend SF Suspending Base, Cherry Flavored, packaged in a) 500mL bottles (NDC 51552-1123-5) and b) 4L bottles (NDC 51552-1123-9), Rx…

    Microbial Contamination of Non-Sterile Product: Product is contaminated with Burkholderia gladioli.

    FDA · DrugFagron, IncNationwide USA and Puerto Rico, Canada, Columbia, FranceOfficial notice →
  7. US
    Drugs & medicalClass II

    Amgen, Inc. recalls MVASI (bevacizumab-awwb), Injection, For Intravenous Infusion After Dilution, 100 mg/4 ml, Single dose vial, Rx only, Manufactured by…

    Defective container: loose crimp defect, potential loss of container integrity.

    FDA · DrugAmgen, Inc.Nationwide in the USA, Egypt and Lithuania.Official notice →
See all drugs & medical recalls →