[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
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD3-6ST |
|---|---|
| Brand / manufacturer | Carefusion 2200 Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0214-2023 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 26 September 2022 |
| EAN / barcode | 10885403019395 |
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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