Class III — Carbon Medical Technologies, Inc.
| Recalling firm | Carbon Medical Technologies, Inc. |
|---|---|
| Registered facility | CARBON MEDICAL TECHNOLOGIES, INC. (the firm's only registered facility) |
| Classification | Class III |
| Status | Ongoing |
| Reason | This recall has been initiated due to a failure to provide an MRI Insert that is to be provided to the patient. |
| Product | BiomarC EX Fiducial Marker System, Catalog Number 040165 |
| Quantity | 25 boxes of 3 devices |
| Distribution | US Nationwide distribution in the state of TN. |
| Initiated | 2024-07-26 |
| Classified | 2024-09-17 |
| Recall number | Z-3161-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class III recall — Carbon Medical Technologies, Inc. (Z-3161-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/95179/
Alerts for Carbon Medical Technologies, Inc.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.