Analogic SyneRad Multi Digital Radiology System, Model AN6150 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Analogic SyneRad Multi Digital Radiology System, Model AN6150
Lot Codes / Batch Numbers
Serial Numbers: 3604-M0120, 5004-M0125, 3204-M0118, 5004-M0126, 4404-M0124, 3204-M0119, 3005-M0131, 2404-M0115, 2404-M0117, 0205-M0130, 3604-M0121, 3904-M0122, 5004-M0127, 3805-M0132, 2705-M0128, 3904-M0123, 0205-M0129
Products Sold
Serial Numbers: 3604-M0120;5004-M0125;3204-M0118; 5004-M0126;4404-M0124;3204-M0119;3005-M0131;2404-M0115;2404-M0117;0205-M0130;3604-M0121;3904-M0122;5004-M0127;3805-M0132;2705-M0128;3904-M0123;0205-M0129
A medical device manufacturer is recalling Analogic SyneRad Multi Digital Radiology System, Model AN6150 due to Potential weld defect in the Overhead Tube Support assembly which connects to the telescoping arm. This could cause the tube assembly to fall, leading. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential weld defect in the Overhead Tube Support assembly which connects to the telescoping arm. This could cause the tube assembly to fall, leading to possiible injury of the user or patient.
Recommended Action
Per FDA guidance
Analogic Corp notified accounts by email on 10/14/2005 and by letter on 10/17/2005. Accounts are requested to stop use and correction will be conducted by a service engineer.
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
AZ, CA, FL, MA, OH, PA, TN, TX
Page updated: Jan 10, 2026