Canon recalls Infinix-8000V systems with CAT-850B or CAT-860B tables due to loose bolts causing table tilting. Affected units have specific serial numbers listed in the recall notice.
Bolts holding the longitudinal movement of catheterization tables may be loose, which may lead to table surface/top tilting.
Canon is recalling Infinix-8000V digital radiography systems with CAT-850B or CAT-860B catheterization tables because bolts holding the table may be loose, leading to tilting. This could cause injury if the table tips during medical procedures.
Loose bolts in the table's longitudinal movement mechanism can cause the table surface to tilt unexpectedly. This tilting could lead to falls or injuries for patients and medical personnel during critical procedures.
Healthcare facilities using the recalled catheterization tables are most at risk. Patients and medical staff could be injured if the table tilts during procedures.
Check if your Infinix-8000V system has a catheterization table labeled CAT-850B or CAT-860B. Affected units have specific serial numbers listed in the recall notice.
Identify the serial number on the catheterization table to confirm if it's in the list of affected units.
Reach out to Canon Medical System, USA, INC. to confirm if your specific unit is affected and get instructions.
The bolts holding the table's movement mechanism may be loose, which can cause the table surface to tilt unexpectedly during use.
Tilting could lead to falls or injuries for patients and medical staff during procedures, especially if the table is not properly secured.
Check the serial number on your catheterization table against the list of affected units provided in the recall notice.
We’ve drafted a message you can send Canon Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2325-2020 — Canon Medical Canon Medical Hello, I own a Canon Medical that is covered by recall Z-2325-2020 from Canon Medical. 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.
