Canon recalls specific catheterization tables (INFX-8000V models) due to potential loose bolts causing table tilt. Affected units may require inspection or repair.
System table may tilt because the bolts that fasten the vertical column and the table top tilting drive unit may become loose.
Canon is recalling certain interventional angiography catheterization tables that may tilt because bolts holding the vertical column and table top can become loose. This could lead to instability during medical procedures.
The bolts that secure the vertical column and the table top tilting drive unit can become loose over time. If the table tilts while in use, it could cause instability during medical procedures, potentially leading to injury to patients or staff.
Healthcare professionals using Canon's INFX-8000V catheterization tables with specific model and serial numbers listed in the recall. Patients undergoing procedures on these tables are at risk if the table tilts unexpectedly.
Check for the model numbers INFX-8000V followed by specific letters (e.g., A6, AA, AC) and the serial numbers listed in the recall notice. The product is used for diagnostic and angiographic procedures on blood vessels.
Compare your table's serial number with the list of affected serial numbers provided in the recall notice.
Reach out to Canon Medical System, USA, INC. for guidance on whether your table is affected and what steps to take next.
The recall is due to bolts that fasten the vertical column and table top tilting drive unit potentially becoming loose, which could cause the table to tilt during use.
The affected models are Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V with specific variants like A6, AA, AC, and others listed in the recall notice.
Check your table's serial number against the list of affected serial numbers provided in the recall notice.
We’ve drafted a message you can send Canon to request your refund or repair — edit it as you like.
Subject: Recall Z-1269-2021 — Canon Canon Hello, I own a Canon that is covered by recall Z-1269-2021 from Canon. 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.
