Edwards SAPIEN 3 Ultra Heart Valve System Recalled for Burst Balloons
Edwards Lifesciences is recalling SAPIEN 3 Ultra Transcatheter Heart Valve Systems due to reports of burst balloons that caused significant difficulty retrieving the device during procedures.
The agency’s classification
FDA (Devices): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall involves a Class I medical device defect (burst balloons) that caused significant difficulty in retrieving the device from patients, which aligns with the rubric criterion for 'significant injury/property-damage reports' or high-risk procedural complications.
Plain-English summary
Edwards Lifesciences, LLC is recalling the SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (23mm) 9630TF23. The recall involves 2,208 units distributed across 12 U.S. states and 17 international locations, including the United Kingdom, Canada, and various European countries.
The recall was initiated to address reports of burst balloons. These incidents have resulted in significant difficulty retrieving the device into the sheath and withdrawing the system from the patient during procedures. The source text does not specify the number of reported incidents or whether any patients suffered injuries or adverse health consequences.
Healthcare providers and facilities that have received this product should contact Edwards Lifesciences for instructions on how to return the devices. The source text does not provide specific contact information or a deadline for the recall action.
The recalled product
- Product
- Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (23mm) 9630TF23 UDI:00690103201246
- Manufacturer
- Edwards Lifesciences, LLC
- Category
- Medical Device — Cardiovascular
- Affected units
- 2,208
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 (1)
- All Lots
Distribution
Part of a larger recall action
This product is one of 4 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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