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SonoSite TEE, 8-3 MHz Transducer labeled: "Tee Transducer... SonoSite, Inc. 21919 30th Drive SE Bothell, WA 98021". The

FDA device recall Z-2191-2010 · posted 2010-08-09 · Terminated

Recall details

Recalling firm
Sonosite, Inc.
Reason for recall
The TEE transesophageal transducer, when connected to a SonoSite M-Turbo Ultrasound System, may exhibit erratic operation of the Scanplane Orientation Indicator on the system display. The indicator may move erratically and not accurately represent the orientation of the TEE transducer array.
Action taken
On August 21, 2008, SonoSite began calling 15 consignees who have purchased the TEE/8-3 MHz Transducer and an M-Turbo 1.1 system. The firm provided instruction to discontinue use the system to 11 consignees and left voice messages to the remaining four consignees. On August 21, 2008, SonoSite sent out the URGENT-MEDICAL DEVICE CORRECTION letter and the Urgent Field Safety Notice to all affected consignees in the US and in foreign countries. The URGENT-MEDICAL DEVICE CORRECTION letter describes the recall product as TEE/8-5 MHz Transducer, SonoSite Part Numbers P05183 and P06841. The letter informed the consignees that the TEE transesophageal transducers may exhibit erratic operation of the Scanplane Orientation Indicator on the system display when it connected to the SonoSite M-Turbo Ultrasound System. The letter instructs consignees to discontinue use of the TEE/8-3MHz Transducer with the M-Turbo (or Micromaxx system) immediately, while the firm is working to create a software solution to resolve the issue and offers customers a software upgrade within 6-8 weeks. The consignees are also advised to forward the recall notice to others who need to be aware of the issue or where the potentially affected devices have been distributed. Customers should call the Technical Support at 1-1-425-951-1330 or 1-877-657-8118 from Monday to Friday, 6 am-5 pm PST or e-mail to service@sonosite.com for any questions regarding the recall.
Root cause
Other
Status
Terminated
Product code
IYO
Quantity affected
357 units
Distribution
Worldwide distribution: USA and countries including Argentina, Austria, Belgium, Brazil, Canada, Chile, Croatia, Czech Republic, Denmark, Finland, France, Germany, India, Iran, Ireland, Israel, Italy,
Date initiated
2008-08-08
Date posted
2010-08-09
Date terminated
2011-08-24
Location
Bothell, WA

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Related 510(k) clearances

RecordFirmDate
SONOSITE MAXX SERIES DIAGNOSTIC ULTRASOUND SYSTEM (K071134)Sonosite,Inc.2007-05-08