Synthes TI Matrix Pre-Bent Maxillary Plate / 2mm ADVMNT/0 — Class II medical device recall Z-2272-2015
Terminated recall by Synthes (USA) Products LLC, reported 2015-08-05, distributed nationwide. The affected part and lot numbers of the TI Matrix Pre-Bent Maxillary Plates may potentially have the incorrec
| Recall number | Z-2272-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Synthes (USA) Products LLC, West Chester, PA, United States |
| Recall initiated | 2015-06-24 |
| Classified | 2015-07-28 |
| Reported by FDA | 2015-08-05 |
| Terminated | 2016-08-18 |
| Distributed | Nationwide (US) |
| Quantity | 31 |
| Lot numbers | 8672260, 8672528, 8673158 |
| Model numbers | 04.511.381, 04.511.382 |
Product
Synthes TI Matrix Pre-Bent Maxillary Plate / 2mm ADVMNT/0.8mm THK/L and Synthes TI Matrix Pre-Bent Maxillary Plate / 2mm ADVMNT/0.8mm THK/R. The Synthes Matrix ORTHOGNATHIC Fixation System is intended for use in selective trauma of the midface and craniofacial skeleton; craniofacial surgery; reconstructive procedures; and selective orthognathic surgery of the maxilla, mandible and chin in adults and children.
Reason for recall
The affected part and lot numbers of the TI Matrix Pre-Bent Maxillary Plates may potentially have the incorrect laser etch denoting the orientation.
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-2272-2015. 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.