# FDA recall Z-2937-2020

> **Hager & Meisinger Gmbh** · Class II · device recall initiated 2020-07-15.

## Product

SINGLES Carbide US-No. FG556; UDI +E0HM26000313140091; STERILE R; Size 009, Length 3.8; 2025-03-18 - Product Usage: Cutting of hard structures in the mouth, such as teeth or bone, it is also intended to cut hard metals, plastics, porcelains, and similar materials intended for use in the fabrication of dental devices.

## Reason for recall

US-dates between the product package label and the bar code display.

## Distribution

US Nationwide distribution including in the states of AZ, CA, FL, IN, NY, PA  and TX.

## Key facts

- **Recall number:** Z-2937-2020
- **Recalling firm:** Hager & Meisinger Gmbh
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-07-15
- **Report date:** 2020-09-16
- **Termination date:** 2022-02-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Neuss, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2937-2020

## Citation

> AI Analytics. FDA recall Z-2937-2020. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/Z-2937-2020. Source: US FDA. Licensed CC0.

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