Graphenano Dental G-Cam product codes with machining errors render the device unusable. Affected units include specific model numbers and serial ranges. Contact Graphenano Dental for details.
Machining error on cams renders the device unusable.
Graphenano Dental G-Cam devices with certain model codes and serial numbers were recalled due to a machining error that makes them unusable. This issue affects denture manufacturing and requires immediate replacement.
A machining error during production causes the G-Cam devices to be unusable. This means they cannot function properly in denture manufacturing processes, rendering them ineffective for their intended purpose.
Denture manufacturers who purchased Graphenano Dental G-Cam devices with the listed model codes and serial numbers are most at risk. The recall impacts dental professionals using these specific products for denture fabrication.
Check for the model codes listed in the recall (e.g., 95 Multichroma 14LB2) and the specific serial numbers provided in the product details. The affected units were sold with the listed lot numbers and reference codes.
Verify your G-Cam device's model code and serial number against the list of affected units provided in the recall notice.
The recall was issued because a machining error renders the Graphenano Dental G-Cam devices unusable for denture manufacturing.
Check your device's model code and serial number against the list of affected units provided in the recall notice.
Contact Graphenano Dental directly for instructions on how to replace the affected device.
We’ve drafted a message you can send Graphenano Dental to request your refund or repair — edit it as you like.
Subject: Recall Z-1192-2024 — Graphenano Dental Graphenano Dental Hello, I own a Graphenano Dental that is covered by recall Z-1192-2024 from Graphenano Dental. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
