Peter Lazic Gmbh: Medical Device Recall in 2024 - (Recall #: Z-1287-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile

Product Classification:

Class II

Date Initiated: July 14, 2023

Date Posted: March 20, 2024

Recall Number: Z-1287-2024

Event ID: 93952

Reason for Recall:

Wrong product coloring. The paddle clips should be blank, but they are colored blue.

Status: Ongoing

Product Quantity: 170 units

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;

Distribution Pattern:

US Nationwide distribution in the state of ME.

Voluntary or Mandated:

Voluntary: Firm initiated