Sterile Radiology Procedure Kits — Class II medical device recall Z-1693-2026
Ongoing recall by Medline Industries, LP, reported 2026-04-08, distributed nationwide. There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise
| Recall number | Z-1693-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2026-02-18 |
| Classified | 2026-03-27 |
| Reported by FDA | 2026-04-08 |
| Distributed | Nationwide (US) |
| Quantity | 420 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10198459071454, 40198459071455 |
| Lot numbers | 25GBB924 |
| Model numbers | DYNDH1491B |
Product
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
Reason for recall
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
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-1693-2026. 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.