Date Initiated by Firm | November 11, 2020 |
Create Date | October 19, 2021 |
Recall Status1 |
Terminated 3 on June 30, 2023 |
Recall Number | Z-0142-2022 |
Recall Event ID |
88691 |
510(K)Number | K203314 |
Product Classification |
System, tomography, computed, emission - Product Code KPS
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Product | Canon PET-CT SCANNER, Cartesion Prime, MODEL PCD-1000A |
Code Information |
Affected serial numbers: 3DA1982001, 3DA2072002, 3DA2072003 |
Recalling Firm/ Manufacturer |
Canon Medical System, USA, INC. 2441 Michelle Dr Tustin CA 92780-7047
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For Additional Information Contact | Terry Schultz 714-730-5000 |
Manufacturer Reason for Recall | A software problem has been identified which could result in the diagnostic imaging system not proceeding to the next actual scan even though automatic start of the next scan is specified. This could result in the diagnostic imaging system failing resulting in rescanning and reinjection of contrast medium. |
FDA Determined Cause 2 | Software design |
Action | On November 11, 2020, Canon Medical Systems visited affected consignees and updated affected software. After completion of the software update, the consignee was provided a "Recall field Modification Instruction" document concerning the correction. |
Quantity in Commerce | 3 units |
Distribution | US Nationwide distribution in the states of NV, AR MN.
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Total Product Life Cycle | TPLC Device Report |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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510(K) Database | 510(K)s with Product Code = KPS
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