Digital RID Plate Reader and Software Product Code: AD400 — Class II medical device recall Z-1055-2017
Terminated recall by The Binding Site Group, Ltd., reported 2017-01-25, distributed in CA, GA, IA, IL, MA, MD, MN, NC…. If a control ring is marked after reading, the software will not flag results that are out of the specified QC
| Recall number | Z-1055-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Binding Site Group, Ltd., Birmingham, United Kingdom |
| Recall initiated | 2012-10-09 |
| Classified | 2017-01-19 |
| Reported by FDA | 2017-01-25 |
| Terminated | 2017-04-04 |
| Distributed | CA, GA, IA, IL, MA, MD, MN, NC, NJ, NY, UT |
| Countries outside the US | DE, ES, FR, GB |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 05051700000376 |
Product
Digital RID Plate Reader and Software Product Code: AD400
Reason for recall
If a control ring is marked after reading, the software will not flag results that are out of the specified QC range.
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-1055-2017. 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.