DIATECH — Class II medical device recall Z-2436-2019
Terminated recall by Coltene /Whaledent AG, reported 2019-09-11, distributed in GA. A single batch of Diatech Diamond dental burs, 856-016-7-F, Round end taper, contain diamond burs with the sam
| Recall number | Z-2436-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Coltene /Whaledent AG, Altstatten Sg, N/A, Switzerland |
| Recall initiated | 2019-07-19 |
| Classified | 2019-08-30 |
| Reported by FDA | 2019-09-11 |
| Terminated | 2021-04-30 |
| Distributed | GA |
| Lot numbers | J22952 |
Product
DIATECH, swiss dental instruments, ROUND END TAPER, 856-016-7-F
Reason for recall
A single batch of Diatech Diamond dental burs, 856-016-7-F, Round end taper, contain diamond burs with the same grit size (fine) and shape (round end taper) but different length.
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-2436-2019. 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.