Edwards Lifesciences Llc One Edwards Way Edwards LifeStent NT Self-Expanding Stent and Delivery System; Models: NT186901(D); NT187901(D); NT186902(D); NT187902(D); NT356901(D); NT357901(D);NT356902; NT357902(D) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Edwards LifeStent NT Self-Expanding Stent and Delivery System; Models: NT186901(D); NT187901(D); NT186902(D); NT187902(D); NT356901(D); NT357901(D);NT356902; NT357902(D)
Brand
Edwards Lifesciences Llc One Edwards Way
Lot Codes / Batch Numbers
All codes.
Products Sold
All codes.
Edwards Lifesciences Llc One Edwards Way is recalling Edwards LifeStent NT Self-Expanding Stent and Delivery System; Models: NT186901(D); NT187901(D); NT1 due to Potential for deployment difficulties.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for deployment difficulties.
Recommended Action
Per FDA guidance
Recall was by voice mail and regular postal service on 4/28/2005 in the USA, in Europe recall began May 2, 2005. Recall notification is complete, unused product is being returned.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026