Cordis US Corp is recalling 12 units of the Vista Brite Tip Guiding Catheter (Judkins Right 4, REF SM7504) because the devices were manufactured at the incorrect length. These catheters are used to introduce medical devices into the heart's blood vessels or peripheral arteries during diagnostic or interventional procedures. No incidents or injuries have been reported in connection with this issue.
A catheter that is shorter or longer than specified may not reach the intended anatomical site or could cause difficulty for the physician during a procedure, potentially leading to surgical delays or clinical complications.
Quantity: 12 units. Catheter intended for intravascular introduction of devices into coronary or peripheral vascular systems.
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 · Raw API Response
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