Nationwide recalls – page 61

• CLEARLINK SYSTEM Solution Set, Non-Vented, two CLEARLINK Luer Activated… recall
  FDA October 22, 2025 · Baxter Healthcare Corporation · Class II
• CLEARLINK System Solution Set, DUO-VENT, CLEARLINK Luer Activated Valve… recall
  FDA October 22, 2025 · Baxter Healthcare Corporation · Class II
• CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves… recall
  FDA October 22, 2025 · Baxter Healthcare Corporation · Class II
• Medical convenience kits IHDC30R D AND C PACK recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits UDPG88W PICC G-TUBE PACK-230209 recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item Number/Description BFCT04X CATARACT PACK -… recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item Number/Description ANSH14AF SHOULDER PACK -… recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item Number/Description HSLM53AB SPINE PACK… recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item Number/Description LKRA40G RADIOLOGY PACK recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item Number/Description FHCP08Y C SECTION PK… recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item Number/Description HSAN63N ANGIO PACK… recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item Number/Description RCGY52D GYN LAPAROSCOPY… recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item Number/Description RCEN25B ENT SDSC 0246972… recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item Number/Description UICL44P ADULT CENTRAL… recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item Number/Description ANCV78BC HEART PACK -… recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item Number/Description EVLH67F LEFT HEART CATH… recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item Number/Description BUCY78E CYSTO PACK… recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item number/ Product description AHLD15X LABOR… recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Medical convenience kits Item number/ Product description AKGN82E GENERAL… recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Basic Biopsy Tray recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Basic Biopsy Tray, Item Number NMBP44L recall
  FDA October 22, 2025 · American Contract Systems Inc · Class II
• Branding is not applied to this product recall
  FDA October 22, 2025 · Spacelabs Healthcare, Inc. · Class II
• Branding is not applied to this product recall
  FDA October 22, 2025 · Spacelabs Healthcare, Inc. · Class II
• Branding is not applied to this product recall
  FDA October 22, 2025 · Spacelabs Healthcare, Inc. · Class II
• Cardiac Workstation 7000 recall
  FDA October 22, 2025 · Philips North America Llc · Class II
• 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
• 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
• Flow Re-Direction Endoluminal Devices: FRED 27 recall
  FDA October 22, 2025 · Microvention Inc. · Class II
• OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE XT160 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• BRONCHOVIDEOSCOPE OLYMPUS BF-Q170 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I