Drugs & medicalClass II

Omega & Delta Co., Inc. recalls Equate Hand Sanitizer (Ethyl Alcohol 62%), 7.5 FL.OZ. (221 mL) UPC 6 81131 05961 9

Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good acceptance criteria established.

Read the official notice →
Date
2023-11-22
Country
United States
Brand
Omega & Delta Co., Inc.
Product
Equate Hand Sanitizer (Ethyl Alcohol 62%), 7.5 FL.OZ. (221 mL) UPC 6 81131 05961 9
Classification
Class II
Units
Distributed in Puerto Rico only.
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2023-11-22
  2. US
    Drugs & medicalClass II

    Atrium Medical Corporation recalls Atrium Advanta V12 Covered Stent System, 10mm x 59mm x 80cm (OUS)-Indicated for restoring and improving the patency of the iliac…

    Balloon-to-catheter weld failure that may cause loss of balloon pressure during stent deployment.

    FDA · DeviceAtrium Medical CorporationForeign: Australia, Belgium, Canada, France, Germany, Greece, Malta,…Official notice →
  3. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls Mobilett Mira wireless (VA20) mobile x-ray system(s)

    Due to the incorrect mounting of the buzzer component, there is no acoustic signal during x ray activation. Otherwise, the system is fully functional, and x ray is applied correctly. By means of the additional visual…

    FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide - WorldwideOfficial notice →
  4. US
  5. 2023-11-15
  6. US
    Drugs & medicalClass II

    Maquet Medical Systems USA recalls Cardiohelp-i, blood oxygenation and carbon dioxide removal system, Part Numbers 701072780 (Cardiohelp-i), 701068550 (Slide Rail Holder)

    It was found that the fixation (weld) employed by the supplier of the nut bolt to the slide rail plate was insufficient. The deficient weld allows the nut bolt to break off from the slide rail plate with slight manual…

    FDA · DeviceMaquet Medical Systems USAUS Nationwide.Official notice →
  7. US
    Drugs & medicalClass II

    Carestream Health, Inc. recalls The DRX-Revolution Mobile X-Ray System is a diagnostic mobile x-ray system utilizing digital radiography (DR) technology. the system…

    There is a potential for unexpected failure of the electrical components within the Carestream Health Inc. generator installed in your DRX-Revolution Mobile X-ray System(s). This can lead to temporary and self…

    FDA · DeviceCarestream Health, Inc.US Nationwide. Global Distribution.Official notice →
  8. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls EVIS EXERA III Gastrointestinal Videoscope

    Sterilization failures when devices are sterilized per the Reprocessing Manual due to lack of drying time for the endoscope channel.

    FDA · DeviceOlympus Corporation of the AmericasNationwide Distribution.Official notice →
See all drugs & medical recalls →