Medical devices recalls – page 57

• CVS Honey Pad Product Name: CVS Honey Pad Model recall
  FDA September 10, 2025 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• MediHoney¿ Product Name: MediHoney¿ HCS Surgical Adhesive Sheet Model recall
  FDA September 10, 2025 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• MediHoney¿ Product Name: MediHoney¿ Hydrogel Adhesive Sheet Model recall
  FDA September 10, 2025 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• MediHoney¿ Product Name: MediHoney¿ Hydrogel Model recall
  FDA September 10, 2025 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• MediHoney¿ Product Name: MediHoney¿ Adhesive Hydrogel Sheet Dressing Model recall
  FDA September 10, 2025 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• MediHoney¿ Product Name: MediHoney¿ HCS Sheet Dressing with Leptospermum… recall
  FDA September 10, 2025 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• MediHoney ¿ Product Name: MediHoney ¿ Tube Model recall
  FDA September 10, 2025 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• MediHoney ¿ Product Name: MediHoney¿ Paste Model recall
  FDA September 10, 2025 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series recall
  FDA September 10, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Philips Allura System configured with a 1 Phase UPS… recall
  FDA September 10, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion System configured with a 1 Phase UPS… recall
  FDA September 10, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Blood Uric Acid Monitoring System Each kit contains 1 meter… recall
  FDA September 10, 2025 · Visgeneer, Inc. · Class II
• Blood Uric Acid Monitoring System Each kit contains 1 meter… recall
  FDA September 10, 2025 · Visgeneer, Inc. · Class II
• LIFEPAK CR2 Part recall
  FDA September 10, 2025 · Physio-Control, Inc. · Class II
• LIFEPAK 1000 Part recall
  FDA September 10, 2025 · Physio-Control, Inc. · Class II
• LIFEPAK 15 Part recall
  FDA September 10, 2025 · Physio-Control, Inc. · Class II
• InPen App, CFN: MMT-8060 (iOS Users) and MMT-8061 (Android Users) recall
  FDA September 10, 2025 · Medtronic MiniMed, Inc. · Class II
• RayStation with the following product descriptions: 1… recall
  FDA September 10, 2025 · Raysearch Laboratories Ab · Class II
• RayStation with the following product descriptions: 1… recall
  FDA September 10, 2025 · Raysearch Laboratories Ab · Class II
• RayStation with the following product descriptions: 1… recall
  FDA September 10, 2025 · Raysearch Laboratories Ab · Class II
• RayStation with the following product descriptions: 1… recall
  FDA September 10, 2025 · Raysearch Laboratories Ab · Class II
• RayStation with the following product descriptions: 1… recall
  FDA September 10, 2025 · Raysearch Laboratories Ab · Class II
• RayStation with the following product descriptions: 1… recall
  FDA September 10, 2025 · Raysearch Laboratories Ab · Class II
• RayStation with the following product descriptions: 1… recall
  FDA September 10, 2025 · Raysearch Laboratories Ab · Class II
• RayStation with the following product descriptions: 1… recall
  FDA September 10, 2025 · Raysearch Laboratories Ab · Class II
• RayStation with the following product descriptions: 1… recall
  FDA September 10, 2025 · Raysearch Laboratories Ab · Class II
• RefleXion X1 Model RXM1000 UDI Codes: (01)00860003983812(11)230504(21)X1100… recall
  FDA September 10, 2025 · Reflexion Medical, Inc. · Class II
• Superion IDS Kit Superion Indirect Decompression System 8MM… recall
  FDA September 10, 2025 · Boston Scientific Neuromodulation Corporation · Class II
• DLP Left Heart Vent Catheter Malleable body and vented connector… recall
  FDA September 10, 2025 · Medtronic Perfusion Systems · Class I
• DLP Left Heart Vent Catheter Malleable body and vented connector… recall
  FDA September 10, 2025 · Medtronic Perfusion Systems · Class I
• DLP Left Heart Vent Catheter Malleable body and vented connector… recall
  FDA September 10, 2025 · Medtronic Perfusion Systems · Class I
• IDM-ARLITE-R. Electrical wheelchair component recall
  FDA September 10, 2025 · mo-Vis BVBA · Class I
• All-round Joystick R-net Light recall
  FDA September 10, 2025 · mo-Vis BVBA · Class I
• IDM-MULTI-R. Electrical wheelchair component recall
  FDA September 10, 2025 · mo-Vis BVBA · Class I
• IDM-MICRO-R. Electrical wheelchair component recall
  FDA September 10, 2025 · mo-Vis BVBA · Class I
• Multi Joystick R-net recall
  FDA September 10, 2025 · mo-Vis BVBA · Class I
• Micro Joystick R-net recall
  FDA September 10, 2025 · mo-Vis BVBA · Class I
• Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+… recall
  FDA September 10, 2025 · Dexcom, Inc. · Class I
• Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+… recall
  FDA September 10, 2025 · Dexcom, Inc. · Class I
• Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM… recall
  FDA September 10, 2025 · Dexcom, Inc. · Class I
• Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM… recall
  FDA September 10, 2025 · Dexcom, Inc. · Class I
• Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM… recall
  FDA September 10, 2025 · Dexcom, Inc. · Class I
• 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
• Novum IQ Syringe Pump, Product Code 40700BAX, infusion pump recall
  FDA September 10, 2025 · Baxter Healthcare Corporation · Class I
• Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump recall
  FDA September 10, 2025 · Baxter Healthcare Corporation · Class I
• Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump recall
  FDA September 10, 2025 · Baxter Healthcare Corporation · Class I
• Medline Kits containing BD SureStep Foley Tray Systems: SKU/Description:… recall
  FDA September 3, 2025 · Medline Industries, LP · Class II
• BD Pyxis Product Name / UDI-DI code recall
  FDA September 3, 2025 · CareFusion 303, Inc. · Class II
• STA - Fibrinogen 5. Model recall
  FDA September 3, 2025 · Diagnostica Stago, Inc. · Class II
• STA-Liquid Anti-Xa 8. Model recall
  FDA September 3, 2025 · Diagnostica Stago, Inc. · Class II