B & K Medical Systems, Inc. Convex Array Transducer used with B-K Ultrasound Scanners Model number: 8667 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Convex Array Transducer used with B-K Ultrasound Scanners Model number: 8667
Brand
B & K Medical Systems, Inc.
Lot Codes / Batch Numbers
Serial Numbers: 1855380, 1855547, 1855548, 1856835, 1856837, 1857171, 1857173, 1857180, 1857427, 1857435, 1857515, 1857748, 1858482, 1858841, 1859751, 1859902, 1860250, 1860262, 1860487, 1860661, 1860858, 1861488, 1861580, 1861581, 1861823, 1861849, 1863084, 1863082
Products Sold
Serial Numbers: 1855380, 1855547, 1855548, 1856835, 1856837, 1857171, 1857173, 1857180, 1857427, 1857435, 1857515, 1857748, 1858482, 1858841, 1859751, 1859902, 1860250, 1860262, 1860487, 1860661, 1860858, 1861488, 1861580, 1861581, 1861823, 1861849, 1863084, 1863082
B & K Medical Systems, Inc. is recalling Convex Array Transducer used with B-K Ultrasound Scanners Model number: 8667 due to Due to a problem with calibration, the device can produce up to 50% elevated acoustic output and up to 2 degrees higher surface temperature. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Due to a problem with calibration, the device can produce up to 50% elevated acoustic output and up to 2 degrees higher surface temperature
Recommended Action
Per FDA guidance
BK Medical notified customers by letter on 4/10/06 via FedEx advising user of the problem and scheduling the software correction by a Service representative visit .
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 noticeDistribution
As reported by FDA
CA, CT, FL, ME, MD, MN, MS, NY, OH, RI, SD, TX, VA
Page updated: Jan 10, 2026