Carefusion 2200 Inc: Medical Device Recall in 2022 - (Recall #: Z-0210-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD2-6ST

Product Classification:

Class II

Date Initiated: September 26, 2022

Date Posted: November 23, 2022

Recall Number: Z-0210-2023

Event ID: 90958

Reason for Recall:

Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.

Status: Ongoing

Product Quantity: 265 units

Code Information:

UDI/DI (01) 10885403019173, ALL LOTS

Distribution Pattern:

US and Australia, Bahrain, Canada, Denmark, Hong Kong, Italy, Japan, Malaysia, Mexico, Norway, Philippines, Saudi Arabia, Singapore, South Africa, Sweden, Thailand, UK, United Arab Emirates

Voluntary or Mandated:

Voluntary: Firm initiated