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Terminated

X-Cel MB-700 A/C Podiatry X-Ray System; X-Cel X-Ray Coporation, 4220 Waller Drive, Crystal Lake, IL 60012

FDA Recall Z-0424-03 · Posted 2003-03-05

Recalling FirmX-Cel X-Ray Corp
Recall StatusTerminated
Product CodeKPR
Date Initiated2002-11-12
Date Terminated2003-02-28
Product Quantity3 units

Reason for Recall

The X-Ray system contained a defective X-Ray tube shield.

Firm Action

Recalled by telephone call on 11/19/2002, with follow-up visits and letters dated 2/27/03. The tube shields were replaced and the x-ray units were recertified.

Root Cause

Other

Distribution Pattern

Northbrook, IL and Frankfort, IL

Official Source

View FDA Recall →

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

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