Maestro Orthodontic Bracket REF711-206-10 QTY — Class II medical device recall Z-2477-2020
Terminated recall by Ortho Organizers, Inc., reported 2020-07-08, distributed in CA, FL, GA, ID, MI, TX. Orthodontic Bracket is mislabeled
| Recall number | Z-2477-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ortho Organizers, Inc., Carlsbad, CA, United States |
| Recall initiated | 2019-04-02 |
| Classified | 2020-06-30 |
| Reported by FDA | 2020-07-08 |
| Terminated | 2022-03-24 |
| Distributed | CA, FL, GA, ID, MI, TX |
| Countries outside the US | CZ, GR, IT, JP, RU, SA |
| Quantity | 104 packages |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00190707016517 |
| Lot numbers | 888666, 898430 |
| Model numbers | 711-206-10 |
Product
Maestro Orthodontic Bracket REF711-206-10 QTY. 10 Rx Only (01)00190707016517 (10)112233 (422)484
Reason for recall
Orthodontic Bracket is mislabeled
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-2477-2020. 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.