# FDA recall Z-2886-2020

> **Materialise N.V.** · Class II · device recall initiated 2020-07-17.

## Product

Match Point System    The Match Point System is intended to by uses as a surgical instrument to assist in the intraoperative positioning of glenoid components used with total and reverse shoulder arthroplasty by referencing anatomic landmarks of the shoulder that are identifiable on preoperative CT-image scans.

## Reason for recall

The procedure side indicated in the top header of the Shoulder Case Planning Report incorrectly indicated the procedure side as "Left" for surgical plans for a "right" procedure side.

## Distribution

Nationwide distribution to: US including PR and International to UK and  Australia.

## Key facts

- **Recall number:** Z-2886-2020
- **Recalling firm:** Materialise N.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-07-17
- **Report date:** 2020-09-02
- **Termination date:** 2020-12-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Heverlee, N/A, Belgium

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2886-2020

## Citation

> AI Analytics. FDA recall Z-2886-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2886-2020. Source: US FDA. Licensed CC0.

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