Paltop Dynamic Dental Implant Dia 3 — Class II medical device recall Z-0836-2020
Terminated recall by Paltop Advanced Dental Solutions Ltd, reported 2020-01-29, distributed in CA, DC, FL, GA, MA, MD, NJ, NY…. Some of the implants were packaged with a Standard Platform Cover Screw instead of a Narrow Platform Cover Scr
| Recall number | Z-0836-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Paltop Advanced Dental Solutions Ltd, Caesarea, Israel |
| Recall initiated | 2019-11-18 |
| Classified | 2020-01-21 |
| Reported by FDA | 2020-01-29 |
| Terminated | 2022-12-27 |
| Distributed | CA, DC, FL, GA, MA, MD, NJ, NY, SC, TX, VA |
| Quantity | 67 |
| UPC / GTIN / UDI-DI | 07290108695649 |
| Lot numbers | WO-011320 |
| Model numbers | 21-70020 |
Product
Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm, Catalog Number 21-70020
Reason for recall
Some of the implants were packaged with a Standard Platform Cover Screw instead of a Narrow Platform Cover Screw. The Standard Platform Cover Screw will not fit in the Narrow Platform implant.
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-0836-2020. 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.