Drugs & medicalClass I

Buzzagogo, LLC recalls Allergy Bee Gone for Kids Nasal Swab Remedy 0.33 FL OZ (10 mL) tubes, UPC Code 860002022116

Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain elevated levels of yeast and mold as well as the presence of Bacillus cereus.

Read the official notice →
Date
2022-07-06
Country
United States
Brand
Buzzagogo, LLC
Product
Allergy Bee Gone for Kids Nasal Swab Remedy 0.33 FL OZ (10 mL) tubes, UPC Code 860002022116
Classification
Class I
Units
Product was distributed via the internet to consumers, retailers and to…
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2022-07-06
  2. US
    Drugs & medicalClass I

    Green Pharmaceuticals, Inc. recalls SnoreStop NasoSpray, 0.3 FL OZ (9 mL), Green Pharmaceuticals Inc. Camarillo, CA 93012, NDC 61152-199-99, UPC 7 69682 29101 3

    Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain microbial contamination identified as Providencia rettgeri.

    FDA · DrugGreen Pharmaceuticals, Inc.Nationwide within the United StatesOfficial notice →
  3. US
    Drugs & medicalClass II

    Macleods Pharma Usa Inc recalls Losartan potassium & Hydrochlorothiazide Tablets 100 mg/25 mg, 30, 90 & 1000 count NDC # 33342-052-07, NDC #33342-052-10 & NDC #…

    CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

    FDA · DrugMacleods Pharma Usa IncProduct was distributed nationwide.Official notice →
  4. US
    Drugs & medicalClass II

    PD-Rx Pharmaceuticals, Inc. recalls Losartan Potassium Tablets, USP 50 mg, 90 Tablets bottles, Rx Only Marketed and Packaged By: PD-Rx Pharmaceuticals, Inc. Oklahoma…

    CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

    FDA · DrugPD-Rx Pharmaceuticals, Inc.NationwideOfficial notice →
  5. 2022-06-29
  6. US
    Drugs & medicalClass II

    CardioTek BV recalls CardioTek EP-TRACER Software V2.x.

    Device did not pass electrical safety testing for adequate insulation.

    FDA · DeviceCardioTek BVWorldwide distribution - US Nationwide distribution in the states of CA, NY,…Official notice →
  7. US
    Drugs & medicalClass II

    Maquet Cardiovascular, LLC recalls INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour surface and…

    Mislabeled: Product labeled as Intergard Woven Straight graft REF IGW0032-30, D: 8 mm, L: 30 cm, contained an Intergard Woven Straight graft of D: 32 mm and L: 30 cm

    FDA · DeviceMaquet Cardiovascular, LLCUS Nationwide distribution in the state of SC.Official notice →
  8. US
    Drugs & medicalClass II

    Beaver Visitec International, Inc. recalls BVI Wet -Field Eraser, 18GA Blunt Tip, 45Deg.-Intended to remove tissue and control bleeding by the use of high frequency…

    Boxes labeled as Wet-Field Eraser, 18GA Blunt Tip, 45Deg., were shipped containing incorrect product a Wet-Field Eraser, 18GA Bevel Tip, Straight, Part Number: 221250

    FDA · DeviceBeaver Visitec International, Inc.US Nationwide distribution in the states of AZ, CA, CT, DC, FL, GA, IN, MA,…Official notice →
See all drugs & medical recalls →