FDA Device recall Z-2436-2019
DIATECH, swiss dental instruments, ROUND END TAPER, 856-016-7-F
- FDA Device
- Class II
- terminated
- Published 2019-09-11
On 2019-09-11 the FDA classified a Class II recall of DIATECH, swiss dental instruments, ROUND END TAPER, 856-016-7-F by Coltene Whaledent Ag, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2436-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-07-19 |
| Published | 2019-09-11 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Coltene Whaledent Ag |
| Distribution | GA |
Product
DIATECH, swiss dental instruments, ROUND END TAPER, 856-016-7-F
Reason
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.
Identifiers
| code_info | Lot/Batch Number J22952 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2436-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.