FDA Device recall Z-1288-2024
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile
- FDA Device
- Class II
- ongoing
- Published 2024-03-20
On 2024-03-20 the FDA classified a Class II recall of L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile by Peter Lazic, citing wrong product coloring. The paddle clips should be blank, but they are colored blue.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1288-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-07-14 |
| Published | 2024-03-20 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Peter Lazic |
| Distribution | US |
Product
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile
Reason
Wrong product coloring. The paddle clips should be blank, but they are colored blue.
Identifiers
| code_info | Model Number: 45.782; UDI/DI: 04250603733799; Serial Numbers: LX61385, LW36020, LW36021, LW36022, LW36023, LW36024, LW36025, LW36026, LW36027; |
|---|
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-1288-2024%22
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