Medical devices recalls – page 52

• Cardiac Workstation 5000 recall
  FDA October 22, 2025 · Philips North America Llc · Class II
• DuoDERM" Extra Thin dressings are highly flexible… recall
  FDA October 22, 2025 · ConvaTec, Inc · Class II
• Airvo 2, REF: PT101US, and myAirvo 2, REF: PT100US… recall
  FDA October 22, 2025 · Fisher & Paykel Healthcare, Ltd. · Class II
• LOGIQ P9 R4.5 ultrasound system with system software version R4.5.7… recall
  FDA October 22, 2025 · GE Medical Systems, LLC · Class II
• LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7… recall
  FDA October 22, 2025 · GE Medical Systems, LLC · Class II
• LOGIQ P10 series with software version R4.5.7 Model Number 5877534 recall
  FDA October 22, 2025 · GE Medical Systems, LLC · Class II
• BioPro Femoral Head Product ID/Description 14089 HEAD FEMORAL 28 SH LT… recall
  FDA October 22, 2025 · BioPro, Inc. · Class II
• BioPro Endo Head (Ceramic) Product ID/Description 13006 ENDO MODULAR… recall
  FDA October 22, 2025 · BioPro, Inc. · Class II
• BioPro Femoral Head (Ceramic heads 28-30) Product ID/Description 19023… recall
  FDA October 22, 2025 · BioPro, Inc. · Class II
• BioPro Bipolar Head Product ID/Description 18130 BIPOLAR HEAD 38MM 18131… recall
  FDA October 22, 2025 · BioPro, Inc. · Class II
• BioPro Endo Head (Metal uni-polar, 38-55) Product Number/Description 10179… recall
  FDA October 22, 2025 · BioPro, Inc. · Class II
• BioPro Femoral Head (Metal 22, 28, 32, 36, 40) cobalt chromium and ceramic… recall
  FDA October 22, 2025 · BioPro, Inc. · Class II
• ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection… recall
  FDA October 22, 2025 · Ethicon Endo Surgery, LLC · Class II
• XERF EFFECTOR 60. Electrosurgical unit recall
  FDA October 22, 2025 · Lutronic Corporation · Class II
• ARVIS Product Name: ARVIS" Shoulder Model recall
  FDA October 22, 2025 · Kico Knee Innovation Company · Class II
• LGX Preconnect with TENACIO Pump with InhibiZone recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class II
• CXR Preconnect with TENACIO Pump with InhibiZone recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class II
• CX Preconnect with TENACIO Pump with InhibiZone recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class II
• LGX Preconnect with TENACIO Pump without InhibiZone recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class II
• CX Preconnect with TENACIO Pump without InhibiZone recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class II
• TENACIO Pump without InhibiZone recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class II
• TENACIO Pump with InhibiZone recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class II
• Medline Adult Anesthesia Set recall
  FDA October 22, 2025 · Medline Industries, LP · Class II
• C-Rex UNO Microinterventional Goniotomy Instrument recall
  FDA October 22, 2025 · Iantrek Inc. · Class II
• Cyclopen Microinterventional Cyclodialysis System recall
  FDA October 22, 2025 · Iantrek Inc. · Class II
• FERNO POWER X2 POWERED AMBULANCE COT, Model recall
  FDA October 22, 2025 · Ferno-Washington Inc · Class II
• The failure occurs if a user on the Omnipod 5 iOS application selects and… recall
  FDA October 22, 2025 · Insulet Corporation · Class II
• Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with… recall
  FDA October 22, 2025 · Contego Medical, Inc · Class II
• TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, F, (UniD Curve F) recall
  FDA October 22, 2025 · Abbott · Class I
• TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, FJ, (BiD Curve F-J) recall
  FDA October 22, 2025 · Abbott · Class I
• TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, DF, (BiD Curve D-F) recall
  FDA October 22, 2025 · Abbott · Class I
• TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, DD, (BiD Curve D-D) recall
  FDA October 22, 2025 · Abbott · Class I
• TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, D, (UniD Curve D) recall
  FDA October 22, 2025 · Abbott · Class I
• Flow Re-Direction Endoluminal Devices: FRED 27 recall
  FDA October 22, 2025 · Microvention Inc. · Class II
• Model Number U228, VISIONIST CRT-P EL MRI recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number U226, VISIONIST CRT-P EL recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number U225 VISIONIST CRT-P EL recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number U128, VALITUDE CRT-P EL MRI recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• Model Number U125, VALITUDE CRT-P EL recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• 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