FDA Device recall Z-1870-2017
Bush DL Ureteral Illuminating Catheter Set Bush SL Ureteral Illuminating Catheter Set
- FDA Device
- Class II
- terminated
- Published 2017-04-26
On 2017-04-26 the FDA classified a Class II recall of Bush DL Ureteral Illuminating Catheter Set Bush SL Ureteral Illuminating Catheter Set by Cook, citing product may overheat, melt, and burn patient.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1870-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-07 |
| Published | 2017-04-26 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Cook |
| Distribution | n/a |
Product
Bush DL Ureteral Illuminating Catheter Set Bush SL Ureteral Illuminating Catheter Set
Reason
Product may overheat, melt, and burn patient.
Identifiers
| code_info | All lots. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1870-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.