Canon Infinix-8000F Catheterization Tables Risk of Table Tilting
Canon recalls Infinix-8000F systems with CAT-850B or CAT-860B catheterization tables due to loose bolts causing table tilting. Affected units have specific serial numbers listed in the recall notice.
Use caution until it’s fixed
Bolts holding the longitudinal movement of catheterization tables may be loose, which may lead to table surface/top tilting.
Contact the company
What happened, in plain English
Canon is recalling Infinix-8000F digital radiography systems with CAT-850B or CAT-860B catheterization tables because bolts holding the table may be loose. This could cause the table surface to tilt, potentially leading to injury during medical procedures. Read more at govinfonow.com/recall/65723-canon-infinix-8000f-catheterization-tables-risk-of-table-tilting.
Source Summary by GovInfoNow · govinfonow.com/recall/65723-canon-infinix-8000f-catheterization-tables-risk-of-table-tilting · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2327-2020
Cite this page
“Canon Infinix-8000F Catheterization Tables Risk of Table Tilting.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/65723-canon-infinix-8000f-catheterization-tables-risk-of-table-tilting. Based on FDA recall #Z-2327-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2327-2020%22&limit=1).
Why it’s dangerous
Loose bolts in the catheterization table can cause the table surface to tilt. This tilting could lead to patient injury or equipment damage during medical procedures if the table is not securely anchored.
Who’s affected
Healthcare professionals using these catheterization tables for medical procedures are most at risk. Patients undergoing procedures with these tables could be affected if the table tilts.
How to tell if you have this one
Check for the specific serial numbers listed in the recall: AGB1692005, AGB17Z2010, AGA1552003, AGB17Y2009, AGB1682004, AGA1492002, AGC1822012, A5C1922001, AGB1712007, AGC1952014, AGB1482001, AGC1822011, BGB1992001, AGC18X2013, AGB16Z2006. These units were sold with the Infinix-8000F system and CAT-850B or CAT-860B tables.
- Brand
Canon Medical- Category
Medical device
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
US Nationwide distribution including in the states of PA, AR, OH, NC, CA, IA, GA, IL, AL, WV, LA, MO, FL, MS, TX, AZ, MA, NJ, MD, NY, NV, OK, WI, PR.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-2325-2020 | Infinix-8000V with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen and lower extremities.; Serial Numbers: A5B1642006, A1B17X2004, A5A1612005, A5B1772009, B5B1962002, A3A1522004, A7B16Y2001, A3A1712011, A5B1792010, A5A1532002, A1A1612003, A3A15Z2007, A5A1552003, A5B16Y2007, A3B1862016, A3B1812013, A3A1662009, A9A16X2004, BTA1922001, A3B1842015, AOB1882001, BMB1942001, AOB1892002, A5B1472001, A5B17Z2011, A3A14X2002, A5A1592004, A3A17Z2012, A5C1832012, A5B16Z2008, A1A1582002, A9A1582002, A1A14X2001, A3A1512003, A7C1812002, ABC18X2002, A3A1592005, UTC14Y2008, A3A15X2006, B5B1942001, A3A1682010, A1C18Z2005, A9A1662003, A3A1492001, A3B1822014, A3A1622008 | 46 |
| Z-2326-2020 | Infinix-8000C with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen and lower extremities.; Serial Numbers: B8B1972001, A9A1592001, A3A14Z2001, AEB1812002, A1B1552001, A9C18Y2007, A3E1922002, B5B1952001, A9C1822006, A9B1622002, A9B1722003, A5C1622001, B3B19Y2001, A1D1772003, B1B19X2001, A5C16Y2002, A9C1822005, A1E1862008, A1D1752002, A1E1832004, A1E1852005, A1E1852006, A5E1862003, AEA17X2001 | 24 |
| Z-2327-2020 | Infinix-8000F with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen and lower extremities.; Serial Numbers: AGB1692005, AGB17Z2010, AGA1552003, AGB17Y2009, AGB1682004, AGA1492002, AGC1822012, A5C1922001, AGB1712007, AGC1952014, AGB1482001, AGC1822011, BGB1992001, AGC18X2013, AGB16Z2006 | 15 |
What to do — step by step
Check Table Serial Number
Look for the serial numbers listed in the recall notice: AGB1692005, AGB17Z2010, AGA1552003, AGB17Y2009, AGB1682004, AGA1492002, AGC1822012, A5C1922001, AGB1712007, AGC1952014, AGB1482001, AGC1822011, BGB1992001, AGC18X2013, AGB16Z2006.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 23 states.
FDA distribution: “US Nationwide distribution including in the states of PA, AR, OH, NC, CA, IA, GA, IL, AL, WV, LA, MO, FL, MS, TX, AZ, MA, NJ, MD, NY, NV, OK, WI, PR.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Arizona, Arkansas, California, Florida, Georgia, Illinois, Iowa, Louisiana, Maryland, Massachusetts, Mississippi, Missouri, Nevada, New Jersey, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, Puerto Rico, Texas, West Virginia, Wisconsin.
Recall timeline
FDA published this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
Do I need to stop using the table immediately?
No, but you should check the serial number to see if your table is affected. If it is, you may need to take action to secure the bolts.
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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-2327-2020 (March 3, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2327-2020 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 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.