Edwards Lifesciences Recalls Swan-Ganz Catheters Due to Guidewire Passage Issues
Edwards Lifesciences is recalling 32,145 Swan-Ganz Thermodilution VIP Catheters because a J-tip guidewire may pass through the distal lumen hub.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall is classified as FDA Class II. The hazard involves a mechanical defect (guidewire passage) in a medical device used for hemodynamic monitoring, which presents a risk of harm, but the source text does not report specific injuries or fatalities.
Plain-English summary
Edwards Lifesciences, LLC is recalling 32,145 units of Swan-Ganz Thermodilution VIP Catheters, Model 151HF7. These devices are used for hemodynamic monitoring in patients. The recall covers units distributed in the United States, Canada, Japan, EMEA, Asia Pacific, and Latin America.
The recall was initiated after the firm received multiple complaints regarding the passage of a J-tip guidewire when inserted through the distal lumen hub of the catheter. The affected product codes are 59163071, 59174300, 59178366, and 59233787.
Healthcare providers and facilities should check their inventory for these specific model numbers and codes. If the affected devices are in use, they should be removed from service and returned to the manufacturer according to the recall instructions.
The recalled product
- Product
- Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 151HF7. For use in patients who require hemodynamic monitoring.
- Manufacturer
- Edwards Lifesciences, LLC
- Category
- Medical Device — Catheter
- Affected units
- 32,145
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- 59163071
- 59174300
- 59178366
- 59233787
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 11 recalled by Edwards Lifesciences, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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