Recall StatusOpen, Classified
Date Initiated2024-03-23
Product Quantity363
Reason for Recall
Ultrasound system with: 1) transesophageal echocardiography transducer (TEE) connected/not selected 2) 1, 2 non-TEE connected 3) Imaging with non-TEE 4) Selected/not selected imaging transducer removed 5) Transducer connected 6) Non-TEE imaging continues, Then though TEE is unselected, it may have power, no temperature monitoring/control, and may result in temperature above limit and patient burns
Firm Action
On 3/23/24, correction notices were distributed to customers who were advised of the following two ways to avoid the condition:
Option 1: To prevent the issue from occurring, when using the TEE transducers, connect directly to the Compact 5000 system using the port on the side of the system as shown in Figure 3 below. The issue is associated with the MPA, therefore by using the port on the Compact 5000 directly, the issue is avoided.
Option 2: Whenever adding a transducer to, or removing a transducer from the MPA, disconnect and reconnect the MPA connector on the Compact 5000 system connector port, followed by a transducer selection on the touch screen. By performing this step when adding or removing a transducer, the monitoring and control systems are re-initialized.
Circulate this URGENT Medical Device Correction Letter to all users of this device within your organization and forward to any organization where potentially affected devices have been transferred so that they are aware of the issue.
In addition, customers were asked to complete and return the response form
[email protected]
A firm representative will contact you to schedule a time for a Field Service Engineer to visit and implement the solution to resolve the issue
For further information or support concerning this issue, please contact your local firm
representative: For North America, contact the Customer Care Solutions Center (1-800-722-9377).
Root Cause
Component change control
Distribution Pattern
Worldwide - US Nationwide distribution including in the states of CA, CO, CT, FL, GA, IL, IN, KS, KY, MA, MD, ME, MI, NC, NH, NM, NY, OH, OK, PA, PR, SC, TN, TX, UT, VA and the countries of Australia, Austria, Bahrain, Brazil, Bulgaria, Canada, Croatia, Czech Republic, Denmark, Finland, France, Germany, Italy, Japan, Lithuania, Netherlands, New Zealand, Oman, Poland, Romania, Slovenia, South Africa, Spain, Sweden, Switzerland, United Kingdom, United Arab Emirates.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.