CLASSIC Radiofrequency Cannula — Class II medical device recall Z-0720-2020
Terminated recall by Abbott Medical, reported 2020-01-01, distributed nationwide. A manufacturing error caused a single lot of 10mm active tip length Cannulas to be labeled as 5mm active tip l
| Recall number | Z-0720-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Abbott Medical, Plymouth, MN, United States |
| Recall initiated | 2019-11-11 |
| Classified | 2019-12-20 |
| Reported by FDA | 2020-01-01 |
| Terminated | 2021-04-01 |
| Distributed | Nationwide (US) |
| Countries outside the US | BM |
| Quantity | 470 devices |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 05415067028693 |
| Lot numbers | 6865795 |
| Model numbers | C-1005-S |
Product
CLASSIC Radiofrequency Cannula - Curved, 10 cm, SMK Compatible Electrode, REF C-1005-S - Product Usage: Disposable Radiofrequency Cannulae are provided in either straight, curved, or curved blunt geometries with a stylet inserted in the cannula. Cannulae are insulated except for the active tip. The active tip determines the size of the radiofrequency lesion.
Reason for recall
A manufacturing error caused a single lot of 10mm active tip length Cannulas to be labeled as 5mm active tip length cannulas.
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-0720-2020. 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.