Skaneateles Falls, NY, United States
Ge Inspection Technologies Llc recalls
1 recall recorded since 2018, most recently on 29 September 2020. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 29 September 2020
- Terminated
- 2 May 2023
- Reason
- 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.
- Distribution
- USA Canada
- Initiated
- FDA Mandated
- Recall number
- Z-0442-2021
- v|tome|x L Series non-destructive testing cabinet x-ray systems
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.