Date Initiated by Firm | September 29, 2020 |
Create Date | November 13, 2020 |
Recall Status1 |
Terminated 3 on May 02, 2023 |
Recall Number | Z-0442-2021 |
Recall Event ID |
86620 |
Product Classification |
Cabinet x-ray, industrial - Product Code RCE
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Product | v|tome|x L Series non-destructive testing cabinet x-ray systems |
Code Information |
v/tome/x L Series (L240, L300 or L450) |
Recalling Firm/ Manufacturer |
Ge Inspection Technologies Llc 721 Visions Dr Skaneateles Falls NY 13153-5314
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Manufacturer Reason for Recall | It was discovered during testing of the v/tome/x L450 system s/n PA1790, that the pre-warning signals does not provide "Audible and visible warning signals within the cabinet" if the "warm up" mode was not completed after initializing the system when first turned on. |
FDA Determined Cause 2 | Radiation Control for Health and Safety Act |
Distribution | USA
Canada |
Total Product Life Cycle | TPLC Device Report |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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