FDA Device recall Z-2206-2015
American Science & Engineering Inc,Gemini Cabinet X-ray system
- FDA Device
- Class II
- terminated
- Published 2015-08-26
On 2015-08-26 the FDA classified a Class II recall of American Science & Engineering Inc,Gemini Cabinet X-ray system by American Science And Engineering, citing during factory testing, we discovered that Gemini systems could, in rare circumstances, experience a fault that leads to a state in which X-rays are being produced but the X-ray i….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2206-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-05-22 |
| Published | 2015-08-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | American Science And Engineering |
| Distribution | CT, DC, DE, FL, GA, MD, ME, MO, MS, NC, NJ, NV, NY, PA, TN, TX, VA |
Product
American Science & Engineering Inc,Gemini Cabinet X-ray system.
Reason
During factory testing, we discovered that Gemini systems could, in rare circumstances, experience a fault that leads to a state in which X-rays are being produced but the X-ray indicator lights (located on the operator's console and on both ends of the tunnel) are not illuminated.
Identifiers
| code_info | Gemini systems |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2206-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.