Normand-Info S.A.S.U.: Medical Device Recall in 2020 - (Recall #: Z-1430-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Remisol Advance running on hardware with Windows XP, Windows 7, Windows Server 2003 and Windows Server 2008 operating systems

Product Classification:

Class II

Date Initiated: August 15, 2019

Date Posted: March 11, 2020

Recall Number: Z-1430-2020

Event ID: 83687

Reason for Recall:

A patch was released for a critical remote code execution vulnerability in remote desktop services. This vulnerability can be exploited remotely without authentication on certain operating systems. An attacker who successfully exploited this vulnerability could execute arbitrary code on the target system; then install programs; view, change, or delete data; or create new accounts with full user rights. If the vulnerability could be exploited locally, it would lock down the computer.

Status: Terminated

Product Quantity: 6479

Code Information:

All serial numbers

Distribution Pattern:

U.S.: NY, AZ, FL, NJ, MA, OH, CA, IL, NC, OK, IN, KY, OR, MI, WI, PA, UT, GA, VA, TX, NE, SD, IA, MN, MD, DE, SC, MT, WV, LA, MO, TN, NM, NV, HI, WA, WY, AL, AR, MS, RI, ID, ME, DC, ND, AK, CO, CT, KS, NH, VT

Voluntary or Mandated:

Voluntary: Firm initiated