C-Max" Cutting Loop Electrodes — Class II medical device recall Z-0585-2017
Terminated recall by C.R. Bard, Inc., reported 2016-11-23, distributed in FL, GA, LA, OH, VA, WA. Defect; The contact part could possibly separate from the electrode affecting to functionality of the device.
| Recall number | Z-0585-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | C.R. Bard, Inc., Covington, GA, United States |
| Recall initiated | 2016-10-12 |
| Classified | 2016-11-16 |
| Reported by FDA | 2016-11-23 |
| Terminated | 2021-10-05 |
| Distributed | FL, GA, LA, OH, VA, WA |
| Quantity | 70 units |
| Lot numbers | NGAN2854, NGAQ5248 |
Product
C-Max" Cutting Loop Electrodes, Storz One-Stem, 24 Fr, .014in., .35 mm, Sterile, Rx only, Manufactured by: C.R. Bard, Inc., Covington, GA 30014.
Reason for recall
Defect; The contact part could possibly separate from the electrode affecting to functionality of the device.
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-0585-2017. 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.