Class II — Paltop Advanced Dental Solutions Ltd
| Recalling firm | Paltop Advanced Dental Solutions Inc. |
|---|---|
| Registered facility | PALTOP ADVANCED DENTAL SOLUTIONS LTD (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | 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. |
| Product | Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm, Catalog Number 21-70020 |
| Quantity | 67 |
| Distribution | The products were distributed to the following US states: CA, DC, FL, GA, MA, MD, NJ, NY, SC, TX, and VA. |
| Initiated | 2019-11-18 |
| Classified | 2020-01-21 |
| Terminated | 2022-12-27 |
| Recall number | Z-0836-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Paltop Advanced Dental Solutions Ltd (Z-0836-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/84412/
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