FDA Device recall Z-1321-2024
Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
- FDA Device
- Class II
- ongoing
- Published 2024-03-27
On 2024-03-27 the FDA classified a Class II recall of Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967 by Preat, citing due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the associated implant.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1321-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-02-09 |
| Published | 2024-03-27 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Preat |
| Distribution | US |
Product
Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
Reason
Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the associated implant.
Identifiers
| code_info | Model Number: 9000967 UDI-DI code: 00842092165867 Lot Numbers: 235650, 234294, 233667, 233885, 233439, and 231489 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1321-2024%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.