Drugs & medicalClass II

Ventana Medical Systems Inc recalls Ventana HE 600 System, automated slide preparer, for use in laboratories.

There is a potential for fluid leak inside the Ventana HE 600 instrument which could result in electrical short and fire

Read the official notice →
Date
2022-07-20
Country
United States
Brand
Ventana Medical Systems
Product
Ventana HE 600 System, automated slide preparer, for use in laboratories.
Classification
Class II
Units
US: AL AR AZ CA CO CT DC FL GA HI IA IL IN KS KY MA MD MI MN MO MS MT NC NE NJ…
Category
Drugs & medical
Source
FDA · Device

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 Details may be shortened or out of date; the official notice is the authoritative source.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.

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