Medical devices recalls – page 33

• Medline medical convenience kits packaged as: 1) CANCER SERVICE PORT KIT… recall
  FDA February 18, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits packaged as: PEDIATRIC CATH SECUREMENT… recall
  FDA February 18, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits packaged as: ADULT CATH SECUREMENT DRSG… recall
  FDA February 18, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits packaged as: ANESTHESIA ARTLINE PACK… recall
  FDA February 18, 2026 · Medline Industries, LP · Class II
• Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON… recall
  FDA February 18, 2026 · Medline Industries, LP · Class I
• Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound… recall
  FDA February 18, 2026 · Medline Industries, LP · Class I
• Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE… recall
  FDA February 18, 2026 · Medline Industries, LP · Class I
• Reprocessed St recall
  FDA February 18, 2026 · Medline Industries, LP · Class I
• Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters:… recall
  FDA February 18, 2026 · Medline Industries, LP · Class I
• Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry… recall
  FDA February 18, 2026 · Medline Industries, LP · Class I
• Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10… recall
  FDA February 18, 2026 · Medline Industries, LP · Class I
• Spectral CT 7500 on Rails recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• Spectral CT recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• IQon Spectral CT recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• Brilliance iCT recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• Brevera Breast Biopsy System Disposable 9 Gauge Needle recall
  FDA February 18, 2026 · Hologic, Inc · Class II
• Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B recall
  FDA February 18, 2026 · Medline Industries, LP · Class II
• Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory… recall
  FDA February 18, 2026 · Medline Industries, LP · Class II
• Molift Product Name: Molift 4-point sling bars (Accessory to mobile… recall
  FDA February 11, 2026 · Etac A/S · Class II
• Molift Product Name: Molift 2-point sling bars (Accessory to mobile… recall
  FDA February 11, 2026 · Etac A/S · Class II
• Molift Product Name: Molift Mover 300 Model recall
  FDA February 11, 2026 · Etac A/S · Class II
• Molift Product Name: Molift Mover 205 Model recall
  FDA February 11, 2026 · Etac A/S · Class II
• Lumipulse ¿-Amyloid Plasma Controls Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse pTau 217 Plasma Controls Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G pTau 217 Plasma Calibrators Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Bubble Sensor for 3/8" x 3/32" tubing recall
  FDA February 11, 2026 · Maquet Cardiopulmonary Gmbh · Class II
• FDR Visionary Suite recall
  FDA February 11, 2026 · FUJIFILM Healthcare Americas Corporation · Class II
• Nasal Jejunal Feeding Tube recall
  FDA February 11, 2026 · Wilson-Cook Medical Inc. · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Product Name: Disposable Triple… recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II