FDA Medical Device Recalls (openFDA)
Canon Medical System, USA, INC.: Canon Aquilion Precision, Model TSX-304A
- Recall number
- Z-1725-2020
- Recalling firm
- Canon Medical System, USA, INC.
- Product
- Canon Aquilion Precision, Model TSX-304A
- Status
- Open, Classified
- Initiated
- 2019-03-25
- Posted
- 2020-04-10
- Terminated
- not on file
- Reason
- Scanning may be interrupted due to an error during execution of the eXam Plan and the system is unable to be shut down normally, resulting in the need to forcibly turn the system power off and reboot. Loss of the acquired raw data would occur.
- Root cause
- Software design
- Action
- Recall letters dated 3/25/2019 were issued on 3/25/2019 via USPS return receipt mail.
- Quantity
- 1 device
- Distribution
- Distribution was made to AK, AR, CA, FL, IA, ID, IL, KS, MA, MD, MI, MN, MO, MT, NC, ND, NH, NY, OH, OK, OR, PA, TN, TX, VT, WA, WI, and WV. There was government and military distribution but no foreign distribution.
- Lot, serial or model codes
- Canon Aquilion Precision, Whole-Body X-Ray CT Scanner, Model TSX-304A, Serial number 2DB1892018.
- 510(k) numbers
- ["K173468"]
- PMA numbers
- not on file
- Product code
- JAK
- Firm FEI
- 2020563
- Firm city
- Tustin
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
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