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Terminated

Analogic SyneRad Multi Digital Radiology System, Model AN6150

FDA Recall Z-0196-06 · Posted 2005-11-24

Recalling FirmAnalogic Corporation
Recall StatusTerminated
Product CodeKPR
Date Initiated2005-10-14
Date Terminated2015-04-14
Product Quantity17 UNITS

Reason for Recall

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.

Firm 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.

Root Cause

Other

Distribution Pattern

AZ, CA, FL, MA, OH, PA, TN, TX,

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K040995SYNERAD MULTI DIGITAL X-RAY SYSTEM, MODEL AN6150Analogic Corp. · 2004-05-25

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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