Class II medical devices recalls – page 14

• MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model recall
  FDA June 17, 2026 · Avanos Medical, Inc. · Class II
• MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL Model recall
  FDA June 17, 2026 · Avanos Medical, Inc. · Class II
• MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model recall
  FDA June 17, 2026 · Avanos Medical, Inc. · Class II
• MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model recall
  FDA June 17, 2026 · Avanos Medical, Inc. · Class II
• MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model recall
  FDA June 17, 2026 · Avanos Medical, Inc. · Class II
• CORFLO Safety PEG Kit with ENFit Connector Model recall
  FDA June 17, 2026 · Avanos Medical, Inc. · Class II
• CORFLO* Safety PEG Kit with ENFit¿ Connector Model recall
  FDA June 17, 2026 · Avanos Medical, Inc. · Class II
• CORFLO* Safety PEG Kit with ENFit¿ Connector Model recall
  FDA June 17, 2026 · Avanos Medical, Inc. · Class II
• CORFLO* Safety PEG Kit with ENFit¿ Connector Model recall
  FDA June 17, 2026 · Avanos Medical, Inc. · Class II
• CORFLO* Safety PEG Kit Model recall
  FDA June 17, 2026 · Avanos Medical, Inc. · Class II
• CORFLO* Safety PEG Kit Model recall
  FDA June 17, 2026 · Avanos Medical, Inc. · Class II
• CORFLO Product Name: CORFLO Safety PEG Kit Model recall
  FDA June 17, 2026 · Avanos Medical, Inc. · Class II
• CORFLO Product Name: CORFLO* Safety PEG Kit Model recall
  FDA June 17, 2026 · Avanos Medical, Inc. · Class II
• SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Product Name: SPORETRAQ… recall
  FDA June 17, 2026 · HF Acquisition Co LLC · Class II
• SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ… recall
  FDA June 17, 2026 · HF Acquisition Co LLC · Class II
• CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model recall
  FDA June 17, 2026 · INSPIREMD Inc · Class II
• CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model recall
  FDA June 17, 2026 · INSPIREMD Inc · Class II
• CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model recall
  FDA June 17, 2026 · INSPIREMD Inc · Class II
• CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model recall
  FDA June 17, 2026 · INSPIREMD Inc · Class II
• CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model recall
  FDA June 17, 2026 · INSPIREMD Inc · Class II
• CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model recall
  FDA June 17, 2026 · INSPIREMD Inc · Class II
• TDC VELOCE", 27G Two Dimensional Cutter - 20k CPM recall
  FDA June 17, 2026 · D.O.R.C. Dutch Opthalmic Research Center Intl B.V. · Class II
• TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM recall
  FDA June 17, 2026 · D.O.R.C. Dutch Opthalmic Research Center Intl B.V. · Class II
• TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM recall
  FDA June 17, 2026 · D.O.R.C. Dutch Opthalmic Research Center Intl B.V. · Class II
• Bicarby" Dialysate recall
  FDA June 17, 2026 · Fresenius Medical Care Holdings, Inc. · Class II
• EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU… recall
  FDA June 17, 2026 · Berlin Heart Gmbh · Class II
• Mahurkar Elite PASS Trays recall
  FDA June 17, 2026 · Mozarc Medical US LLC · Class II
• Allia Moveo angiographic X-ray system recall
  FDA June 17, 2026 · GE Medical Systems, LLC · Class II
• Allia IGS Pulse angiographic X-ray system recall
  FDA June 17, 2026 · GE Medical Systems, LLC · Class II
• Allia IGS 7 Pulse angiographic X-ray system recall
  FDA June 17, 2026 · GE Medical Systems, LLC · Class II
• Allia IGS 5 Pulse angiographic X-ray system recall
  FDA June 17, 2026 · GE Medical Systems, LLC · Class II
• Allia IGS 3 Pulse angiographic X-ray system recall
  FDA June 17, 2026 · GE Medical Systems, LLC · Class II
• Plum Duo Precision IV Pump, 40002-0403 recall
  FDA June 17, 2026 · ICU Medical, Inc. · Class II
• Plum Duo Infusion Pump, 40002-0401 recall
  FDA June 17, 2026 · ICU Medical, Inc. · Class II
• Plum Solo Precision IV Pump, 40001-0401 recall
  FDA June 17, 2026 · ICU Medical, Inc. · Class II
• Fresh Roast Systems ColorTrack recall
  FDA June 17, 2026 · Fresh Roast Systems Inc · Class II
• Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model recall
  FDA June 10, 2026 · Intuitive Surgical, Inc. · Class II
• Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model recall
  FDA June 10, 2026 · SSC- Surgical Specialties Corporation · Class II
• TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model recall
  FDA June 10, 2026 · Grace Medical, Inc. · Class II
• Aligned Medical AMS16835 Fluids Kit RX recall
  FDA June 10, 2026 · Windstone Medical Packaging, Inc. · Class II
• MAC 5 A4 Resting ECG Analysis System 855001-001 recall
  FDA June 10, 2026 · GE Medical Systems China Co., Ltd. · Class II
• DeRoyal Industries Inc recall
  FDA June 10, 2026 · DeRoyal Industries Inc · Class II
• BD Pyxis MedBank Mini recall
  FDA June 10, 2026 · CareFusion 303, Inc. · Class II
• BD Pyxis MedBank Tower recall
  FDA June 10, 2026 · CareFusion 303, Inc. · Class II
• BD Pyxis MedStation ES Tower recall
  FDA June 10, 2026 · CareFusion 303, Inc. · Class II
• BD Pyxis Mini Main recall
  FDA June 10, 2026 · CareFusion 303, Inc. · Class II
• BD Pyxis Anesthesia Station 4000 recall
  FDA June 10, 2026 · CareFusion 303, Inc. · Class II
• BD Pyxis Anesthesia Station ES recall
  FDA June 10, 2026 · CareFusion 303, Inc. · Class II
• BD Pyxis MedStation ES recall
  FDA June 10, 2026 · CareFusion 303, Inc. · Class II
• BD Pyxis MedStation 4000 recall
  FDA June 10, 2026 · CareFusion 303, Inc. · Class II
• Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2))… recall
  FDA June 10, 2026 · Bayer Medical Care, Inc. · Class II
• Phothera 200, Phototherapy Devices indicated for use to treat diagnosed… recall
  FDA June 10, 2026 · Daavlin Distributing Company · Class II
• Digital Angiography System Trinias:UD150G-40 / D150GC-40 recall
  FDA June 10, 2026 · Shimadzu Medical Systems · Class II
• Arvis Hip & Knee 2.0 Instrument Set recall
  FDA June 10, 2026 · Kico Knee Innovation Company · Class II
• Arvis Hip & Knee 3.0 Instrument Set recall
  FDA June 10, 2026 · Kico Knee Innovation Company · Class II
• Philips Azurion 7M20, Model Numbers: 722079… recall
  FDA June 10, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion 7M12, Model Numbers: 722078… recall
  FDA June 10, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion 7B20/15, Model Numbers: 722068… recall
  FDA June 10, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion 7B12/12, Model Numbers: 722067… recall
  FDA June 10, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion 5M20, Model Numbers: 722228 with Software release R2.2.0… recall
  FDA June 10, 2026 · Philips Medical Systems Nederland B.V. · Class II