Canon Medical System, USA, INC.: CAS-930A Flat Panel Monitor (FPD) used in conjunction with the Canon Interventional Angiography System, Model numbers: Infinix-8000C and Infinix-8000H - 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.

Recall number

Z-0532-2021

Recalling firm

Canon Medical System, USA, INC.

Product

CAS-930A Flat Panel Monitor (FPD) used in conjunction with the Canon Interventional Angiography System, Model numbers: Infinix-8000C and Infinix-8000H - 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.

Status

Terminated

Initiated

2020-10-08

Posted

not on file

Terminated

2022-12-06

Reason

There is a potential that the cable of the Flat panel detector may break during a procedure which may cause the x-ray device to stop before the examination is completed. This could result in a delay with procedure and/or potential damage to the patients blood vessels due to removal without visibility.

Root cause

Component design/selection

Action

On 10/08/2020, Canon Medical Systems sent a "Urgent: Medical Device Correction" Notification to all affected consignees via Fax. In addition to informing consignees about the correction, Canon as consignees to take the following actions: 1. On a daily basis, prior to the installation of the new cable with the modified routing, please perform the start-up inspection described in the Operation Manual to confirm that the FPD up and down movement operates normally. Additionally, please have available a mobile device which can perform fluoroscopy such as a surgical C-arm device or another catheter inspection/IVR room. 2. If the above event occurs, please stop using the device and contact your Canon service representative. . 3. Please share this information with all users and reviewing radiologist as well as clinical engineering and the biomedical group at your facility. 4. Please complete and return the attached form and fax it to the toll free number at the top of the form. This form may also be sent via email to RAffairs@us.medical.canon. 5. Thank you for your prompt attention to this matter. If you have any questions, please feel free to contact Terry Schultz Regulatory Affairs Manager at (800) 421-1968 or your local Canon service representative at (800) 521-1968.

Quantity

14 units

Distribution

US Nationwide distribution including in the states of LA, CA, CO, WV, GA, NH, FL, PA, WI, MN, ID.

Lot, serial or model codes

Affected Serial Numbers:  1 AFA1662001,  2 AFB1872005, 3 AFB1832003,  4 AFB1872004,  5 AFB1892006,  6 BFA18Y7001,  7 AEA17X2001,  8 AFA1692002,  9 AEB1812002,  10 BFA1932001,  11 BFB1952003,  12 BFB1942002,  13 BFB1972004,  14 BFB1972005,  15 AFB1892007,  16 BEC2032001,  17 BFC2062007,  18 BFC2062008,  19 BHA1992001,  20 BFC2012006

510(k) numbers

["K152697","K181804"]

PMA numbers

not on file

Product code

OWB

Firm FEI

2020563

Firm city

Tustin

Firm state

CA

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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