Radiofrequency Grounding Pad — Class II medical device recall Z-0664-2020
Terminated recall by Abbott Medical, reported 2019-12-18, distributed nationwide. Affected lots were manufactured with the protective release liner in an incorrect orientation. When attempting
| Recall number | Z-0664-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Abbott Medical, Plymouth, MN, United States |
| Recall initiated | 2019-10-14 |
| Classified | 2019-12-10 |
| Reported by FDA | 2019-12-18 |
| Terminated | 2021-07-19 |
| Distributed | Nationwide (US) |
| Quantity | 8,940 devices |
| UPC / GTIN / UDI-DI | 05415067028914 |
| Lot numbers | 810319004, 810319005, 810319021 |
Product
Radiofrequency Grounding Pad, REF RF-DGP-L
Reason for recall
Affected lots were manufactured with the protective release liner in an incorrect orientation. When attempting to remove this disposable release liner, a clear film may be left on the grounding pad which may interfere with patient skin contact and lead to uneven heating.
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-0664-2020. 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.