# FDA recall Z-2637-2020

> **Neocis Inc.** · Class II · device recall initiated 2020-05-14.

## Product

DRW-0739-01: Gen 2 Posterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended to provide assistance in both the planning (pre-operative) and the surgical (intra-operative) phases of dental implantation surgery.

## Reason for recall

The LRUL and LLUR posterior chairside splints and LLUR anterior chairside splints may be mislabeled.

## Distribution

US Nationwide distribution including in the states of AZ, CA, FL, NY, and NH

## Key facts

- **Recall number:** Z-2637-2020
- **Recalling firm:** Neocis Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-05-14
- **Report date:** 2020-07-22
- **Termination date:** 2021-07-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Miami, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2637-2020

## Citation

> AI Analytics. FDA recall Z-2637-2020. Retrieved 2026-07-10 from https://api.ai-analytics.org/recall/Z-2637-2020. Source: US FDA. Licensed CC0.

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