FDA Device recall Z-0708-2020
Rhondium OVC3 One Visit Crown, Model FDI 24/25L USA 12/13L A2 HT, Nonsterile, Rx. The firm name on the label is Rhondium Ltd., Katikati, Ne…
- FDA Device
- Class II
- completed
- Published 2019-12-25
On 2019-12-25 the FDA classified a Class II recall of Rhondium OVC3 One Visit Crown, Model FDI 24/25L USA 12/13L A2 HT, Nonsterile, Rx. The firm name on the label is Rhondium Ltd., Katikati, Ne… by Rhondium, citing the product was mislabeled with an incorrect expiration date.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0708-2020 |
| Classification | Class II |
| Status | completed |
| Initiated | 2019-01-31 |
| Published | 2019-12-25 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Rhondium |
| Distribution | IL, NM, TX, WI |
Product
Rhondium OVC3 One Visit Crown, Model FDI 24/25L USA 12/13L A2 HT, Nonsterile, Rx. The firm name on the label is Rhondium Ltd., Katikati, New Zealand.
Reason
The product was mislabeled with an incorrect expiration date.
Identifiers
| code_info | Lot numbers 1832-1099 and 1828-0982. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0708-2020%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.