Canon Infinix DP-i Catheter Table Recall: Liquid Spills Cause Unintended Tilts
Canon Medical recalls Infinix DP-i (CAT-870B) catheterization tables that tilt unexpectedly when liquid spills into the tilt console, potentially causing patient falls. Affected models were sold from 2005-2008.
Use caution until it’s fixed
Table tilts without operator involvement as a result of liquid spilling into tilt console triggering a short circuit.
Contact the company
What happened, in plain English
Canon Medical is recalling certain catheterization tables that tilt unexpectedly when liquid spills into the tilt console. This could cause the table to move suddenly, potentially leading to patient falls during medical procedures. Read more at govinfonow.com/recall/69025-canon-infinix-dp-i-catheter-table-recall-liquid-spills-cause.
Source Summary by GovInfoNow · govinfonow.com/recall/69025-canon-infinix-dp-i-catheter-table-recall-liquid-spills-cause · Updated August 20, 2026 · FDA enforcement record: FDA #Z-0360-2020
Cite this page
“Canon Infinix DP-i Catheter Table Recall: Liquid Spills Cause Unintended Tilts.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/69025-canon-infinix-dp-i-catheter-table-recall-liquid-spills-cause. Based on FDA recall #Z-0360-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0360-2020%22&limit=1).
Why it’s dangerous
Liquid spilling into the tilt console creates a short circuit that causes the table to tilt without operator control. This unintended movement could lead to patient falls during medical procedures requiring precise positioning.
Who’s affected
Healthcare professionals using the Infinix DP-i (CAT-870B) catheterization tables with the Infinix-8000F X-ray system are most at risk. Patients undergoing angiography procedures may be affected if the table tilts unexpectedly.
How to tell if you have this one
Check for model number CAT-870B with serial numbers from the list provided (e.g., 99D08X2101, 99D0582039). These tables were sold between May 2005 and October 2008.
- Brand
Canon Medical- Category
Medical device
What to do — step by step
Check Table Model
Identify the model number on your catheterization table; affected units are CAT-870B with specific serial numbers listed in the recall.
Contact Manufacturer
Reach out to Canon Medical for guidance on whether your table is affected and what steps to take next.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 7 states.
FDA distribution: “Worldwide distribution - US Nationwide distribution in the states of AL, CT, FL, IL, OR, PA, and TX; and country of Netherlands.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Connecticut, Florida, Illinois, Oregon, Pennsylvania, Texas.
Recall timeline
FDA terminated this recall 3.3 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-0360-2020 (February 8, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0360-2020 to see it in context.
- Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.