Toshiba American Medical Systems Inc SSH-880CV Aplio Artida System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SSH-880CV Aplio Artida System
Brand
Toshiba American Medical Systems Inc
Lot Codes / Batch Numbers
2031, 2032, 2033, 2048, 2049, 2056, 2069, 2070, 2071, 2072, 2073, 2074, 2075, 2076, 2077, 2078, 2079, 2080, 2087, 2088, 2103, 2104, 2105, 2106, 2707, 2108, 2119, 2120, 2123, 2124, 2204, 2205, 2206
Products Sold
2031, 2032, 2033, 2048, 2049, 2056, 2069, 2070, 2071, 2072, 2073, 2074, 2075, 2076, 2077, 2078, 2079, 2080, 2087, 2088, 2103, 2104, 2105, 2106, 2707, 2108, 2119, 2120, 2123, 2124, 2204, 2205, 2206
Toshiba American Medical Systems Inc is recalling SSH-880CV Aplio Artida System due to Toshiba America Medical Systems (TAMS) is initiating a field correction on the SSH-880CV Aplio Artida System due to a problem related to a wrong measu. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Toshiba America Medical Systems (TAMS) is initiating a field correction on the SSH-880CV Aplio Artida System due to a problem related to a wrong measurement value display in using with DICOM viewer. When an image is transferred from this system in DICOM transfer and a measurement is performed on a Doppler image in the DICOM viewer, measured values such as VTI (Velocity Time Integral) and PI/RI
Recommended Action
Per FDA guidance
The software will be replaced. To accomplish this, Toshiba America Medical Systems (TAMS) will notify consignees via USPS return receipt mail. The letter contains a return reply form that is to be faxed to TAMS for retention. For questions or concerns, please contact your Toshiba representative or the firm at (714) 730-5000.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026