DX-D 600 — Class II medical device recall Z-2175-2014
Terminated recall by AGFA Healthcare Corp., reported 2014-08-20, distributed in DC, GA, IN, KS, KY, MA, NJ, SC…. Some customers reported that while using the DX-D600 in room or exam preparation, the Overhead Tube Crane (OTC
| Recall number | Z-2175-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AGFA Healthcare Corp., Greenville, SC, United States |
| Recall initiated | 2014-07-02 |
| Classified | 2014-08-09 |
| Reported by FDA | 2014-08-20 |
| Terminated | 2015-06-04 |
| Distributed | DC, GA, IN, KS, KY, MA, NJ, SC, VA |
| Countries outside the US | CA |
| Quantity | 17 units |
| Serial numbers | A5430000015, A5430000020, A5430000030, A5430000042, A5430000052, A5430000061, A5430000066, A5430000067, A5430000079, A5430000081, A5430000085, A5430000089, A5430000095, A5430000096, A5430000105, A5430000125, A5430000131 |
Product
DX-D 600 - DXD Imaging Package Product Usage: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, check abdomen and other both parts.
Reason for recall
Some customers reported that while using the DX-D600 in room or exam preparation, the Overhead Tube Crane (OTC) showed increased velocity and uncontrolled longitudinal movement.
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-2175-2014. 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.