Bush DL Ureteral Illuminating Catheter Set Bush SL Ureteral… — Class II medical device recall Z-1870-2017
Terminated recall by Cook Inc., reported 2017-04-26. Product may overheat, melt, and burn patient.
| Recall number | Z-1870-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cook Inc., Bloomington, IN, United States |
| Recall initiated | 2017-03-07 |
| Classified | 2017-04-20 |
| Reported by FDA | 2017-04-26 |
| Terminated | 2018-10-16 |
| Countries outside the US | AE, BE, BR, BS, CA, CH, CL, CN, CY, CZ, DE, DK, DO, EG, ES, FI, FR, GB, GR, GT, HK, HN, HU, IE, IL, IT, KW, MA, MX, NO, NZ, PA, PT, PY, RO, SA, SE, TT |
| Quantity | 19,756 |
| Reason classes | device malfunction |
Product
Bush DL Ureteral Illuminating Catheter Set Bush SL Ureteral Illuminating Catheter Set
Reason for recall
Product may overheat, melt, and burn patient.
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-1870-2017. 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.