Tapered SwissPlus Implant System — Class II medical device recall Z-1823-2017
Terminated recall by Zimmer Dental Inc, reported 2017-04-26. It was manufactured with the minor diameter of the internal thread that is below specification.
| Recall number | Z-1823-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Dental Inc, Carlsbad, CA, United States |
| Recall initiated | 2017-03-20 |
| Classified | 2017-04-14 |
| Reported by FDA | 2017-04-26 |
| Terminated | 2017-11-01 |
| Quantity | 188 units |
| Lot numbers | 63498673 |
| Model numbers | SPB10 |
Product
Tapered SwissPlus Implant System, Model No. SPB10
Reason for recall
It was manufactured with the minor diameter of the internal thread that is below specification.
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-1823-2017. 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.