Z-1287-2024 Class II Ongoing
FDA device recall Z-1287-2024 was initiated by Peter Lazic Gmbh on July 14, 2023 and is designated Class II. Reason for recall: Wrong product coloring. The paddle clips should be blank, but they are colored blue. The recall status is ongoing. Affected quantity: 170 units.
Recall Details
- Product Type
- Devices
- Report Date
- March 20, 2024
- Initiation Date
- July 14, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 170 units
Product Description
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile
Reason for Recall
Wrong product coloring. The paddle clips should be blank, but they are colored blue.
Distribution Pattern
US Nationwide distribution in the state of ME.
Code Information
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;