FDA Device recall Z-1693-2026
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
- FDA Device
- Class II
- ongoing
- Published 2026-04-08
On 2026-04-08 the FDA classified a Class II recall of Sterile Radiology Procedure Kits, Model Number DYNDH1491B by Medline Industries, citing there is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1693-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-02-18 |
| Published | 2026-04-08 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
Reason
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
Identifiers
| code_info | UDI-DI: (CS) 40198459071455, (EA) 10198459071454; Lot Number: 25GBB924 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1693-2026%22
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