FDA Medical Device Recalls (openFDA)
Analogic Corporation: Analogic SyneRad Multi Digital Radiology System, Model AN6150
- Recall number
- Z-0196-06
- Recalling firm
- Analogic Corporation
- Product
- Analogic SyneRad Multi Digital Radiology System, Model AN6150
- Status
- Terminated
- Initiated
- 2005-10-14
- Posted
- 2005-11-24
- Terminated
- 2015-04-14
- Reason
- 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.
- Root cause
- Other
- Action
- 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.
- Quantity
- 17 UNITS
- Distribution
- AZ, CA, FL, MA, OH, PA, TN, TX,
- Lot, serial or model codes
- 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
- 510(k) numbers
- ["K040995"]
- PMA numbers
- not on file
- Product code
- KPR
- Firm FEI
- 1220672
- Firm city
- Peabody
- Firm state
- MA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28