FDA Device recall Z-0019-2020
Paltop Advanced Plus Dental Implant Dia 6.0mm L10mm Catalog Number: 20-70024P
- FDA Device
- Class II
- terminated
- Published 2019-10-09
On 2019-10-09 the FDA classified a Class II recall of Paltop Advanced Plus Dental Implant Dia 6.0mm L10mm Catalog Number: 20-70024P by Paltop Advanced Dental Solutions, citing surface micro/nano topography on some of the implants contained within this lot may not be consistently present over the entire surface of the implant.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0019-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-05-30 |
| Published | 2019-10-09 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Paltop Advanced Dental Solutions |
| Distribution | AL, AZ, CA, CO, FL, GA, MA, MD, MO, MT, NJ, NM, NY, OH, SC, VA |
Product
Paltop Advanced Plus Dental Implant Dia 6.0mm L10mm Catalog Number: 20-70024P
Reason
Surface micro/nano topography on some of the implants contained within this lot may not be consistently present over the entire surface of the implant.
Identifiers
| code_info | Lot Number: W0-008254 UDI: 729010869611020-70024P |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0019-2020%22
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