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[Recalled] CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD3-6ST — Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently m… | FDA 2022-09-26

recall fda device united-states

This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.

Recall details

ProductCareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD3-6ST
Brand / manufacturerCarefusion 2200 Inc
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0214-2023
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date26 September 2022
EAN / barcode10885403019395

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Carefusion 2200 Inc

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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