Boston Scientific Corporation recalls – page 2

• Model Number S722, ALTRUA 2 DR EL Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number S702, ALTRUA 2 DR SL Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number S701 ALTRUA 2 SR SL Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number L131, ESSENTIO DR EL MRI Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number L121 ESSENTIO DR EL Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number L111, ESSENTIO DR SL MRI Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number L110, ESSENTIO SR SL MRI Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number L101, ESSENTIO DR SL Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number L100, ESSENTIO SR SL Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number L231, PROPONENT DR EL MRI Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number L221 PROPONENT DR EL Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number L211 PROPONENT DR SL MRI Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number L210 PROPONENT SR SL Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number L209 PROPONENT DR (VDD) SL Pacemaker recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• PROPONENT DR SL (Model L201) recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• PROPONENT SR SL (Model L200) recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• ACCOLADE DR EL MRI (Model L331) recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• ACCOLADE DR EL (Model L321) recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• ACCOLADE DR SL MRI (Model L311) recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• ACCOLADE SR SL MRI (Model L310) recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• ACCOLADE DR SL (Model L301) recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• ACCOLADE SR SL (Model L300) recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Extractor Pro RX Retrieval Balloon Catheter recall
  FDA October 1, 2025 · Boston Scientific Corporation · Class II
• Preventive Maintenance (PM) Kit ICEFX, Material Number (UPN) SPRPM8000 recall
  FDA September 17, 2025 · Boston Scientific Corporation · Class II
• ICEfx Cryoablation System, portable helium-free desktop cryoablation unit… recall
  FDA September 17, 2025 · Boston Scientific Corporation · Class II
• Boston Scientific UroMax Ultra Kit, Material Numbers (UPN): 1… recall
  FDA September 17, 2025 · Boston Scientific Corporation · Class II
• Boston Scientific NephroMax Kit, Material Numbers (UPN): 1. M0062101180 recall
  FDA September 17, 2025 · Boston Scientific Corporation · Class II
• Boston Scientific Encore Advantage Kit, Material Numbers (UPN): 1… recall
  FDA September 17, 2025 · Boston Scientific Corporation · Class II
• Boston Scientific Encore 26 Inflation Device, Material Numbers (UPN): 1… recall
  FDA September 17, 2025 · Boston Scientific Corporation · Class II
• WATCHMAN TruSteer Access System, US, Material Number (UPN)… recall
  FDA September 10, 2025 · Boston Scientific Corporation · Class I
• WATCHMAN FXD Curve Access System Dbl, US, Material Number (UPN) M635TU80020 recall
  FDA September 10, 2025 · Boston Scientific Corporation · Class I
• WATCHMAN FXD Curve Access System Sgl, US, Material Number (UPN) M635TU80010 recall
  FDA September 10, 2025 · Boston Scientific Corporation · Class I
• WATCHMAN TruSeal Access System ANT, US, Material Number (UPN) M635TU70040 recall
  FDA September 10, 2025 · Boston Scientific Corporation · Class I
• WATCHMAN TruSeal Access System DBL, US, Material Number (UPN) M635TU70020 recall
  FDA September 10, 2025 · Boston Scientific Corporation · Class I
• WATCHMAN TruSeal Access System SGL, US, Material Number (UPN) M635TU70010 recall
  FDA September 10, 2025 · Boston Scientific Corporation · Class I
• WATCHMAN FXD Curve Access Sys Dbl, OUS, Material Number (UPN) M635TS80020 recall
  FDA September 10, 2025 · Boston Scientific Corporation · Class I
• WATCHMAN FXD Curve Access Sys Sgl, OUS, Material Number (UPN) M635TS80010 recall
  FDA September 10, 2025 · Boston Scientific Corporation · Class I
• WATCHMAN TruSeal Access System ANT, OUS, Material Number (UPN) M635TS70040 recall
  FDA September 10, 2025 · Boston Scientific Corporation · Class I
• WATCHMAN TruSeal Access System DBL, OUS, Material Number (UPN) M635TS70020 recall
  FDA September 10, 2025 · Boston Scientific Corporation · Class I
• WATCHMAN TruSeal Access System SGL, OUS, Material Number (UPN) M635TS70010 recall
  FDA September 10, 2025 · Boston Scientific Corporation · Class I
• RELIANCE 4-FRONT, endocardial cardioversion/defibrillation and pace/sense… recall
  FDA August 27, 2025 · Boston Scientific Corporation · Class I
• ENDOTAK RELIANCE G/SG with 4-SITE Connector… recall
  FDA August 27, 2025 · Boston Scientific Corporation · Class I
• ENDOTAK RELIANCE G/SG, transvenous defibrillation lead… recall
  FDA August 27, 2025 · Boston Scientific Corporation · Class I
• FARAWAVE 1.0 Pulsed Field Ablation Catheter, Product ID M004PF41M401 recall
  FDA August 20, 2025 · Boston Scientific Corporation · Class II
• Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding… recall
  FDA August 20, 2025 · Boston Scientific Corporation · Class I
• Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F… recall
  FDA July 16, 2025 · Boston Scientific Corporation · Class II
• VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201… recall
  FDA July 16, 2025 · Boston Scientific Corporation · Class II
• VersaCross RF Wire (VXW) recall
  FDA July 16, 2025 · Boston Scientific Corporation · Class II
• VersaCross Access Solution (VXSK), Product Description and ID: VXSK (180J… recall
  FDA July 16, 2025 · Boston Scientific Corporation · Class II
• IceSeed 1.5 CX NEEDLE OUS, Cryoablation Needle recall
  FDA May 7, 2025 · Boston Scientific Corporation · Class II
• IceSeed 1.5 CX NEEDLE US, Cryoablation Needle recall
  FDA May 7, 2025 · Boston Scientific Corporation · Class II
• IceSeed 1.5 CX S NEEDLE OUS, Cryoablation Needle recall
  FDA May 7, 2025 · Boston Scientific Corporation · Class II
• IceSeed 1.5 CX S NEEDLE US, Cryoablation Needle recall
  FDA May 7, 2025 · Boston Scientific Corporation · Class II
• HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm… recall
  FDA February 5, 2025 · Boston Scientific Corporation · Class II
• HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm… recall
  FDA February 5, 2025 · Boston Scientific Corporation · Class II
• HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm… recall
  FDA February 5, 2025 · Boston Scientific Corporation · Class II
• HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm… recall
  FDA February 5, 2025 · Boston Scientific Corporation · Class II
• HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN:… recall
  FDA February 5, 2025 · Boston Scientific Corporation · Class II
• HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN:… recall
  FDA February 5, 2025 · Boston Scientific Corporation · Class II
• AXIOS Stent and Delivery System 15mmx10mm UPN: M00553750 recall
  FDA February 5, 2025 · Boston Scientific Corporation · Class II