DX-D600 — Class II medical device recall Z-1738-2017
Terminated recall by AGFA Healthcare Corp., reported 2017-04-12, distributed in AL, CA, DC, FL, GA, HI, IL, IN…. One of the dent markers from the DX-D600 dropped down from the overhead rail.
| Recall number | Z-1738-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AGFA Healthcare Corp., Greenville, SC, United States |
| Recall initiated | 2016-05-02 |
| Classified | 2017-04-05 |
| Reported by FDA | 2017-04-12 |
| Terminated | 2017-04-10 |
| Distributed | AL, CA, DC, FL, GA, HI, IL, IN, KS, LA, MA, MN, MO, NJ, NM, NV, NY, OH, OK, OR, SC, TN, TX, VA |
| Countries outside the US | CA |
| Quantity | 81 units |
Product
DX-D600 - DXD Imaging Package
Reason for recall
One of the dent markers from the DX-D600 dropped down from the overhead rail.
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-1738-2017. 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.