FDA Device recall Z-1287-2024
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, 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, 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-1287-2024 |
| 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, Sterile
Reason
Wrong product coloring. The paddle clips should be blank, but they are colored blue.
Identifiers
| code_info | Model Number: S.45.782; UDI/DI: 04250603734697; Serial Numbers: LX61400, LX61401, LX63366, LX63368, LX63369, LX63370, L…Model Number: S.45.782; UDI/DI: 04250603734697; Serial Numbers: LX61400, LX61401, LX63366, LX63368, LX63369, LX63370, LX63371, LX63372, LX63373, LX63374, LX63375, LX65981, LX65982, LX65983, LX65984, LX66073, LX66074, LX66075, LX61372, LX61373, LX61374, LX61375, LX61376, LX61377, LX61378, LX61379, LX61380, LX61381, LX61382, LX61383, LX61384, LX61385, LX61386, LX61387, LX61388, LX61389, LX61389, LX61390, LX61391, LX61392, LX61393, LX61394, LX61395, LW50566, LW50567, LW50568, LX72845, LX72846, LX72847, LX72848, LX72849, LX72850, LX72851, LX72852, LX72853, LX72854; |
|---|
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-1287-2024%22
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