Peter Lazic Gmbh has recalled 221 units of its L-Aneurysm Clip TITANIUM Paddle-Clips because they were manufactured with the wrong color coding. These surgical clips, including 170 sterile units (Model S.45.782) and 51 non-sterile units (Model 45.782), feature blue paddle clips when they should have remained blank/uncolored. Because surgeons use color coding to identify the specific mechanical properties of these permanent implants, the incorrect color could lead to the selection of the wrong clip during a procedure. If you are a healthcare provider or patient who has received one of these clips, please contact the manufacturer or your hospital's surgical department immediately for guidance.
The incorrect blue coloring on these titanium clips may lead a surgeon to misidentify the device's technical specifications. This error could result in the application of a clip with unintended closing force or sizing during critical aneurysm surgery, potentially leading to surgical complications or device failure.
Manufacturer notification and correction
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
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Sources: FDA iRES ยท Raw API Response
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