Toshiba Aquilion CT System Recall for Data Loss Risk
Toshiba is recalling 459 Aquilion CT Systems because specific scanning operations may prevent raw data from being saved.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the hazard is a data integrity issue (loss of raw data) rather than a direct physical injury or high-risk pathogen, fitting the criteria for moderate severity.
Plain-English summary
Toshiba American Medical Systems Inc is recalling 459 units of the Toshiba Aquilion CT System TSX-302A. The recall involves systems running software version 6.0 or later. These devices were distributed throughout the United States, including Puerto Rico.
The recall is due to a software issue where acquired raw data may not be saved if two specific operations are performed during multi-phase helical scanning. This defect could result in the loss of diagnostic data.
Healthcare facilities should contact Toshiba American Medical Systems Inc for instructions on how to address this issue. Consumers are not directly affected as this is a medical device used in clinical settings.
The recalled product
- Product
- Toshiba Aquilion CT System TSX-302A
- Manufacturer
- Toshiba American Medical Systems Inc
- Hazard
- Affected units
- 459
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- system software V6.0 or later
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 6 recalled by Toshiba American Medical Systems Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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