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V. Mueller CD3-5STRecalls & reported problems

Carefusion 2200, Inc · V. Mueller GENESIS FULL-LENGTH CONTAINER 23 X 12" (58.4 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE · Class 2

All models of V. Mueller (47)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Recalls naming this device

  1. Sep 26, 2022Open, Classified

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

    Z-0213-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Other Sterilization wrap containers, trays, cassettes & other accessories devices

All Sterilization wrap containers, trays, cassettes & other accessories devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page