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[Recalled] Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 151HF7. For use in patients who require hemodynamic monitoring. — The device is being recalled because the firm received multiple complaints rela… | FDA 2012-05

recall fda device united-states

A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.

Recall details

ProductEdwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 151HF7. For use in patients who require hemodynamic monitoring.
Brand / manufacturerEdwards Lifesciences, LLC
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2197-2012
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date11 May 2012
EAN / barcode59163071

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: The device is being recalled because the firm received multiple complaints related to passage of a J-tip guidewire when inserted through the distal lumen hub of the catheter.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Edwards Lifesciences, LLC

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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