Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

Mobilett XP, mobile X-ray system, Model number 1818363

FDA Recall Z-0751-2007 · Posted 2007-04-19

Recall StatusTerminated
Product CodeIZL
Date Initiated2007-03-21
Date Terminated2007-08-07
Product Quantity5 units

Reason for Recall

Mounting bolts for tank fork assembly and collimator flange may become loose.

Firm Action

Siemens Service Personnel are visiting each consignee, beginning March 21, 2007, to replace the required mounting bolts and tighten them according to required torque specifications.

Root Cause

Other

Distribution Pattern

The products were shipped to medical facilities nationwide.

Official Source

View FDA Recall →

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

↑