# FDA recall Z-0836-2020

> **Paltop Advanced Dental Solutions Ltd** · Class II · device recall initiated 2019-11-18.

## 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.

## Distribution

The products were distributed to the following US states:  CA, DC, FL, GA, MA, MD, NJ, NY, SC, TX, and VA.

## Key facts

- **Recall number:** Z-0836-2020
- **Recalling firm:** Paltop Advanced Dental Solutions Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-11-18
- **Report date:** 2020-01-29
- **Termination date:** 2022-12-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Caesarea, Israel

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0836-2020

## Citation

> AI Analytics. FDA recall Z-0836-2020. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-0836-2020. Source: US FDA. Licensed CC0.

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