FDA Device recall Z-1055-2017
Digital RID Plate Reader and Software Product Code: AD400
- FDA Device
- Class II
- terminated
- Published 2017-01-25
On 2017-01-25 the FDA classified a Class II recall of Digital RID Plate Reader and Software Product Code: AD400 by The Binding Site Group, citing if a control ring is marked after reading, the software will not flag results that are out of the specified QC range.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1055-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-10-09 |
| Published | 2017-01-25 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | The Binding Site Group |
| Distribution | CA, GA, IA, IL, MA, MD, MN, NC, NJ, NY, UT |
Product
Digital RID Plate Reader and Software Product Code: AD400
Reason
If a control ring is marked after reading, the software will not flag results that are out of the specified QC range.
Identifiers
| code_info | UDI 05051700000376 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
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All The Binding Site Group recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1055-2017%22
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