Medical devices recalls – page 6

• Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen recall
  FDA August 26, 2026 · Siemens Healthcare Diagnostics Products Ltd. · Class II
• Halyard LAVH PACK, Model recall
  FDA August 26, 2026 · AVID Medical, Inc. · Class II
• GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662 recall
  FDA August 26, 2026 · Maquet Critical Care AB · Class II
• Suture Cinch Long 1pk recall
  FDA August 26, 2026 · Boston Scientific Corporation · Class II
• OverStitch Suture Cinch, 1pk recall
  FDA August 26, 2026 · Boston Scientific Corporation · Class II
• TD Navio Maxi Speech Generating Device Model recall
  FDA August 26, 2026 · Tobii Dynavox Llc · Class II
• TD Navio Midi Speech Generating Device Model recall
  FDA August 26, 2026 · Tobii Dynavox Llc · Class II
• Arrow-LOK Implant recall
  FDA August 26, 2026 · Arrowhead DE LLC · Class II
• Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2… recall
  FDA August 26, 2026 · Kico Knee Innovation Company · Class II
• Cardiac Workstation 7000. Product Number: 860441 recall
  FDA August 26, 2026 · Philips North America Llc · Class II
• Cardiac Workstation 5000. Product Number: 860439 recall
  FDA August 26, 2026 · Philips North America Llc · Class II
• Dentsply Sirona Capsule Mixer Model No recall
  FDA August 26, 2026 · SDI Limited · Class II
• One-Piece Guedel Airway, size 000, ISO 3.5, Light Green recall
  FDA August 26, 2026 · Intersurgical Inc · Class II
• One-Piece Guedel Airway, size 00, ISO 5.0, Blue recall
  FDA August 26, 2026 · Intersurgical Inc · Class II
• Hamilton Microlab STAR Liquid Handler recall
  FDA August 26, 2026 · Foundation Medicine, Inc. · Class II
• EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050… recall
  FDA August 26, 2026 · Covidien, LP · Class II
• Ami HTX recall
  FDA August 26, 2026 · Spectral Instruments Inc · Class II
• Lago X recall
  FDA August 26, 2026 · Spectral Instruments Inc · Class II
• BD Needle Kit for Powered Driver 15mm x 15Ga recall
  FDA August 26, 2026 · Bard Access Systems, Inc. · Class I
• Cardinal Health Presource Kits: 1) BASIC PACK recall
  FDA August 19, 2026 · Cardinal Health 200, LLC · Class II
• Cardinal Health Presource Kits: 1) KIT, MER NEURO BACK recall
  FDA August 19, 2026 · Cardinal Health 200, LLC · Class II
• Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 2 recall
  FDA August 19, 2026 · Cardinal Health 200, LLC · Class II
• Cardinal Health Presource Kits: 1) SEPTO RHINO PACK recall
  FDA August 19, 2026 · Cardinal Health 200, LLC · Class II
• Cardinal Health Presource Kits: 1) ENT TRAY recall
  FDA August 19, 2026 · Cardinal Health 200, LLC · Class II
• Cardinal Health Presource Kits: 1) NEWNAN SMR PACK recall
  FDA August 19, 2026 · Cardinal Health 200, LLC · Class II
• Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC PACK recall
  FDA August 19, 2026 · Cardinal Health 200, LLC · Class II
• Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT recall
  FDA August 19, 2026 · Cardinal Health 200, LLC · Class II
• 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code:… recall
  FDA August 19, 2026 · Bd Switzerland Sarl · Class II
• ERBECRYO 2 Cryosurgical Unit Model recall
  FDA August 19, 2026 · Erbe USA Inc · Class II
• ProNephro AKI (NGAL) Reagent Kit (100 tests) recall
  FDA August 19, 2026 · Bioporto Diagnostics A/S · Class II
• BIOFIRE Respiratory Panel 2.1 (RP2.1) recall
  FDA August 19, 2026 · BioFire Diagnostics, LLC · Class II
• Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm… recall
  FDA August 19, 2026 · Straumann USA LLC · Class II
• Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE… recall
  FDA August 19, 2026 · Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
• OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source… recall
  FDA August 19, 2026 · OBP Medical Corporation · Class II
• Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232, 722233… recall
  FDA August 19, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068… recall
  FDA August 19, 2026 · Philips Medical Systems Nederland B.V. · Class II
• GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box recall
  FDA August 19, 2026 · Terumo Medical Corporation · Class II
• GM Helix Implant, Endosseous Dental Implant Article No recall
  FDA August 19, 2026 · Straumann USA LLC · Class II
• Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035… recall
  FDA August 19, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL… recall
  FDA August 19, 2026 · Remel Europe Ltd. · Class II
• Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12"… recall
  FDA August 19, 2026 · Medline Industries, LP · Class II
• Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count… recall
  FDA August 19, 2026 · Medline Industries, LP · Class II
• Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5", 150 count… recall
  FDA August 19, 2026 · Medline Industries, LP · Class II
• Medline Micro-Kill Bleach Germicidal Bleach Wipes,7" x 8", 150 count… recall
  FDA August 19, 2026 · Medline Industries, LP · Class II
• Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX recall
  FDA August 19, 2026 · Covidien, LP · Class II
• Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623 recall
  FDA August 19, 2026 · Covidien, LP · Class II
• Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31… recall
  FDA August 19, 2026 · Covidien, LP · Class II
• V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING… recall
  FDA August 19, 2026 · Covidien, LP · Class II
• V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336… recall
  FDA August 19, 2026 · Covidien, LP · Class II
• Boston Scientific Enhance Transcarotid/Peripheral Access Kit recall
  FDA August 19, 2026 · Galt Medical Corporation · Class II
• Xhibit Product Name: Xhibit Central Station Model recall
  FDA August 19, 2026 · Spacelabs Healthcare, Inc. · Class II
• GORE VIABIL Short Wire Biliary Endoprosthesis, Model No recall
  FDA August 19, 2026 · W L Gore & Associates, Inc. · Class II
• GORE VIABIL Short Wire Biliary Endoprosthesis, Model No recall
  FDA August 19, 2026 · W L Gore & Associates, Inc. · Class II
• navify Digital Pathology (on-prem) v2.5, Material Number 10092343001… recall
  FDA August 19, 2026 · Ventana Medical Systems, Inc. · Class II
• BOBBY Balloon Guide Catheter recall
  FDA August 19, 2026 · Microvention Inc. · Class II
• Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection… recall
  FDA August 19, 2026 · Spectra Medical Devices, Llc · Class I
• Baxter Duo-Vent Solution Set and Male Luer Lock Adapter… recall
  FDA August 19, 2026 · Baxter Healthcare Corporation · Class I
• Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with… recall
  FDA August 12, 2026 · Contego Medical, Inc · Class II
• Blom-Singer Classic Indwelling Voice Prosthesis, 16Fr/10 mm recall
  FDA August 12, 2026 · Freudenberg Medical, LLC · Class II
• Blom-Singer Classic Indwelling Voice Prosthesis, 16Fr/10 mm recall
  FDA August 12, 2026 · Freudenberg Medical, LLC · Class II