ParaPost Plus 25 Titanium Alloy Spiral Vented and Serrated Posts… — Class II medical device recall Z-0376-2019
Terminated recall by Coltene Whaledent Inc, reported 2018-11-14, distributed in CA, IL, NV, NY, PA, WA. ParaPost Plus Titanium Posts contain stainless steel post that are a size 4
| Recall number | Z-0376-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Coltene Whaledent Inc, Cuyahoga Falls, OH, United States |
| Recall initiated | 2018-08-21 |
| Classified | 2018-11-02 |
| Reported by FDA | 2018-11-14 |
| Terminated | 2020-04-10 |
| Distributed | CA, IL, NV, NY, PA, WA |
| Countries outside the US | CA |
| Quantity | 30 packets |
| Lot numbers | I33012 |
| Model numbers | P2845B |
Product
ParaPost Plus 25 Titanium Alloy Spiral Vented and Serrated Posts Catalog Number: P2845B Dental Posts are implanted into teeth for dental restoration purposes. The normal procedure requires a hole to be drilled into the tissue of a tooth with an intraoral drill prior to installation.
Reason for recall
ParaPost Plus Titanium Posts contain stainless steel post that are a size 4
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-0376-2019. 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.