KaVo Dental recalls cone-beam CT systems with firmware versions 2.1.0 and 2.1.1 due to a defect that may cause improper imaging. Affected units should be checked for the specific firmware versions.
ORTHOPANTOMOGRAPH OP 3D device has a defect in the device firmware versions 2.1.0 and 2.1.1
KaVo Dental is recalling cone-beam CT systems with firmware versions 2.1.0 and 2.1.1 because of a defect that could lead to improper imaging. This recall affects dental imaging equipment used in medical settings.
The defect in the firmware versions 2.1.0 and 2.1.1 could cause improper imaging results. This may lead to inaccurate diagnoses or treatment plans for patients. The exact impact on patient safety is not specified in the recall notice.
Dental clinics and healthcare facilities using KaVo Dental cone-beam CT systems with firmware versions 2.1.0 or 2.1.1 are most at risk. Patients receiving dental imaging with these systems may be affected.
Check if your cone-beam CT system has firmware versions 2.1.0 or 2.1.1. The recall covers KaVo Dental cone-beam CT systems sold with these specific firmware versions.
Identify the firmware version on your cone-beam CT system to see if it is 2.1.0 or 2.1.1.
This recall affects KaVo Dental cone-beam CT systems with firmware versions 2.1.0 or 2.1.1. If your system has these versions, it is affected.
The recall does not specify a remedy, so you should check with KaVo Dental for further instructions.
The recall states a defect that may cause improper imaging, but it does not specify risks of injury or serious harm.
We’ve drafted a message you can send KaVo Dental to request your refund or repair — edit it as you like.
Subject: Recall Z-1101-2019 — KaVo Dental KaVo Dental Hello, I own a KaVo Dental that is covered by recall Z-1101-2019 from KaVo 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.