# FDA recall Z-2425-2020

> **Zest Anchors LLC** · Class II · device recall initiated 2019-11-22.

## Product

LOCATOR OVERDENTURE IMPLANT SYSTEM  STERILE R  Rx Only QTY 1 .

## Reason for recall

The abutment provided with the Implant System may be out of specification, which could lead to a small gap occurring between the implant and abutment on assembly in the patient.

## Distribution

US Nationwide Distribution in the state of: WI; VA; OH; IL; GA; NC; KS; NJ; CA; WA; OK; MO and Puerto Rico     OUS:  Switzerland, Germany, Mexico, Poland, and Thailand

## Key facts

- **Recall number:** Z-2425-2020
- **Recalling firm:** Zest Anchors LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-11-22
- **Report date:** 2020-07-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Carlsbad, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2425-2020

## Citation

> AI Analytics. FDA recall Z-2425-2020. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-2425-2020. Source: US FDA. Licensed CC0.

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