Data Foundry

Medical device recalls 2020

Canon Aquilion Prime SP — Class II medical device recall Z-1724-2020

Ongoing recall by Canon Medical System, USA, INC., reported 2020-04-22, distributed in AK, AR, CA, FL, IA, ID, IL, KS…. Scanning may be interrupted due to an error during execution of the eXam Plan and the system is unable to be s

Recall numberZ-1724-2020
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmCanon Medical System, USA, INC., Tustin, CA, United States
Recall initiated2019-03-25
Classified2020-04-16
Reported by FDA2020-04-22
DistributedAK, 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, WV
Quantity10 devices
Serial numbers1LB1882086, 1LB1882087, 1LB1882088, 1LB1882090, 1LB1882092, 1LB1892093, 1LB18X2109, 1LB18X2111, 1LB18X2129, 1OB1892102
Model numbersTSX-303B

Product

Canon Aquilion Prime SP, Model TSX-303B

Reason for recall

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1724-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.