YXLON Cheetah cabinet X-Ray System Product Usage: The products are… — Class II medical device recall Z-2105-2019
Terminated recall by Comet Technologies Usa Inc, reported 2019-08-14, distributed nationwide. Failure to meet the requirement of the performance standard for cabinet x-ray systems (21 CFR 1020.40) for a d
| Recall number | Z-2105-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Comet Technologies Usa Inc, Shelton, CT, United States |
| Recall initiated | 2018-10-01 |
| Classified | 2019-08-07 |
| Reported by FDA | 2019-08-14 |
| Terminated | 2024-06-13 |
| Distributed | Nationwide (US) |
| Quantity | 77 |
Product
YXLON Cheetah cabinet X-Ray System Product Usage: The products are generally used for non-destructive testing and quality control
Reason for recall
Failure to meet the requirement of the performance standard for cabinet x-ray systems (21 CFR 1020.40) for a door interlock that causes physical disconnection of the power supply using only the movement of the door.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2105-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.