AGFA DX-D 100 is a mobile digital radiography x-ray system — Class II medical device recall Z-1745-2015
Terminated recall by AGFA Healthcare Corp., reported 2015-06-17, distributed in AL, CA, DC, FL, GA, IA, IL, KY…. When using the DX-D 100 unit, sporadic unintended movements caused by an electrostatic discharge of the unit t
| Recall number | Z-1745-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AGFA Healthcare Corp., Greenville, SC, United States |
| Recall initiated | 2015-05-29 |
| Classified | 2015-06-10 |
| Reported by FDA | 2015-06-17 |
| Terminated | 2017-01-18 |
| Distributed | AL, CA, DC, FL, GA, IA, IL, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, SC, TN, TX, VA, WI, WV, WY |
| Quantity | 233 units |
Product
AGFA DX-D 100 is a mobile digital radiography x-ray system
Reason for recall
When using the DX-D 100 unit, sporadic unintended movements caused by an electrostatic discharge of the unit to the ground may occur.
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-1745-2015. 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.