RecallRadar

FDA Device recall Z-0360-2020

Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) - Product Usage: The catheterization table is used with Infinix-8000F…

On 2019-11-20 the FDA classified a Class II recall of Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) - Product Usage: The catheterization table is used with Infinix-8000F… by Canon Medical System Usa, citing table tilts without operator involvement as a result of liquid spilling into tilt console triggering a short circuit.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0360-2020
ClassificationClass II
Statusterminated
Initiated2019-02-08
Published2019-11-20
Last updated2026-09-13 11:55 UTC
CompanyCanon Medical System Usa
DistributionUS

Product

Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) - Product Usage: The catheterization table is used with Infinix-8000F System (Interventional Angiography System), to position patient during diagnostic and interventional x-ray angiography.

Reason

Table tilts without operator involvement as a result of liquid spilling into tilt console triggering a short circuit.

Identifiers

code_info
Model CAT-870B D053991 Serial No. Manufacture Date 99D08X2101 October 2008 99D0582039 August 2005 99D076…Model CAT-870B D053991 Serial No. Manufacture Date 99D08X2101 October 2008 99D0582039 August 2005 99D0762072 June 2007 99D0852090 May 2008 99D07Y2078 November 2007 99D0812081 January 2008 99D0582042 August 2005 99D0552033 May 2005 D551206 May 2005

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0360-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.