Match Point System The Match Point System is intended to by uses as a… — Class II medical device recall Z-2886-2020
Terminated recall by Materialise N.V., reported 2020-09-02, distributed nationwide. The procedure side indicated in the top header of the Shoulder Case Planning Report incorrectly indicated the
| Recall number | Z-2886-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Materialise N.V., Heverlee, N/A, Belgium |
| Recall initiated | 2020-07-17 |
| Classified | 2020-08-26 |
| Reported by FDA | 2020-09-02 |
| Terminated | 2020-12-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, GB |
| Quantity | 128 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2886-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.