FDA Device recall Z-2025-2025
PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, Sterile
- FDA Device
- Class II
- ongoing
- Published 2025-07-02
On 2025-07-02 the FDA classified a Class II recall of PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, Sterile by Limacorporate S P A, citing there is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2025-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-05-19 |
| Published | 2025-07-02 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Limacorporate S P A |
| Distribution | US |
Product
PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, Sterile
Reason
There is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing.
Identifiers
| code_info | Lot number 2421400/UDI: 08033390201834 |
|---|
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-2025-2025%22
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