AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 is… — Class II medical device recall Z-1487-2013
Terminated recall by AGFA Corp., reported 2013-06-12, distributed nationwide. Customers could potentially experience intermittent, unintended and illogical movement when using the product.
| Recall number | Z-1487-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AGFA Corp., Greenville, SC, United States |
| Recall initiated | 2013-05-15 |
| Classified | 2013-06-06 |
| Reported by FDA | 2013-06-12 |
| Terminated | 2014-12-31 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 104 |
Product
AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 is indicated for use in providing diagnostic quality images to aid the physician with diagnosis. Systems can be used with MUSICA2 image processing to create radiographic images of the skeleton including skull, spinal column and extremities: chest, abdomen, and other body parts.
Reason for recall
Customers could potentially experience intermittent, unintended and illogical movement when using the product.
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-1487-2013. 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.