# FDA recall Z-1019-2019

> **AAP Implantate Ag** · Class II · device recall initiated 2019-01-11.

## Product

aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20    Product Usage:  Surgical instruments are intended to aid in the insertion of bone plates and screws as well as for reduction and support during orthopedic surgeries. If not otherwise specified, instruments are intended for multiple use.

## Reason for recall

There is the potential for the Lambotte chisel to break at the welded piece parts of the chisel body and knocking plate.

## Distribution

Worldwide Distribution - US Nationwide in the state of Texas and country of Germany

## Key facts

- **Recall number:** Z-1019-2019
- **Recalling firm:** AAP Implantate Ag
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-01-11
- **Report date:** 2019-03-27
- **Termination date:** 2022-05-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Berlin, N/A, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1019-2019

## Citation

> AI Analytics. FDA recall Z-1019-2019. Retrieved 2026-06-01 from https://api.ai-analytics.org/recall/Z-1019-2019. Source: US FDA. Licensed CC0.

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