Medical devices recalls – page 18

• GE HealthCare ApexPro v6.0 eDelivery Software recall
  FDA June 3, 2026 · GE Medical Systems Information Technologies Inc · Class II
• GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA recall
  FDA June 3, 2026 · GE Medical Systems Information Technologies Inc · Class II
• GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA recall
  FDA June 3, 2026 · GE Medical Systems Information Technologies Inc · Class II
• GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER recall
  FDA June 3, 2026 · GE Medical Systems Information Technologies Inc · Class II
• GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit… recall
  FDA June 3, 2026 · GE Medical Systems Information Technologies Inc · Class II
• GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL recall
  FDA June 3, 2026 · GE Medical Systems Information Technologies Inc · Class II
• Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002 recall
  FDA June 3, 2026 · Medtronic Neuromodulation · Class II
• Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001 recall
  FDA June 3, 2026 · Medtronic Neuromodulation · Class II
• HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3 recall
  FDA June 3, 2026 · Devicor Medical Products Inc · Class II
• Automated Impella Controller (AIC) with the below product descriptions and… recall
  FDA June 3, 2026 · Abiomed, Inc. · Class I
• Medline kits containing Huons Co recall
  FDA June 3, 2026 · Medline Industries, LP · Class I
• Medline kits containing Huons Co recall
  FDA June 3, 2026 · Medline Industries, LP · Class I
• Medline kits containing Huons Co recall
  FDA June 3, 2026 · Medline Industries, LP · Class I
• Medline kits containing Huons Co recall
  FDA June 3, 2026 · Medline Industries, LP · Class I
• Medline kits containing Huons Co recall
  FDA June 3, 2026 · Medline Industries, LP · Class I
• Medline kits containing Huons Co recall
  FDA June 3, 2026 · Medline Industries, LP · Class I
• Medline kits containing Huons Co recall
  FDA June 3, 2026 · Medline Industries, LP · Class I
• Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771… recall
  FDA June 3, 2026 · O&M Halyard, Inc. · Class II
• Automated Impella Controller (AIC) recall
  FDA June 3, 2026 · Abiomed, Inc. · Class I
• RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers:… recall
  FDA June 3, 2026 · Bolton Medical Inc. · Class I
• Integris-Allura system recall
  FDA May 27, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Allura system recall
  FDA May 27, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion system recall
  FDA May 27, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Silastic Foley Catheters Silastic Brand Foley Catheter 30cc recall
  FDA May 27, 2026 · C.R. Bard Inc · Class II
• Philips Azurion systems not configured with an optional auxiliary pan… recall
  FDA May 27, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• OneLIF Interbody Cage ( recall
  FDA May 27, 2026 · Novapproach Spine, LLC · Class II
• Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock… recall
  FDA May 27, 2026 · ICU Medical, Inc. · Class II
• Tangent Endoscopy, Tangent Single Use Digital Catheter recall
  FDA May 27, 2026 · Tangent Endoscopy, LLC · Class II
• Swan-Ganz Pacing Catheter, Models: D200F7 recall
  FDA May 27, 2026 · Becton Dickinson & Co. · Class II
• Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P recall
  FDA May 27, 2026 · Becton Dickinson & Co. · Class II
• Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75… recall
  FDA May 27, 2026 · Becton Dickinson & Co. · Class II
• Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer… recall
  FDA May 20, 2026 · Medtronic Neuromodulation · Class II
• LVIS Intraluminal Support Device recall
  FDA May 20, 2026 · Microvention Inc. · Class II
• Medtronic Marinr Steerable, Product Number 72402 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• Daig Livewire Steerable BDB, Product Number 401918… recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• Daig Livewire Steerable, Product Number 401932 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• Daig Livewire Steerable, Product Number 401923 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• Daig Livewire Steerable, Product Number 401915 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• Daig Livewire Steerable, Product Number 401914 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• Daig Livewire Steerable, Product Number 401908 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• Daig Livewire Steerable, Product Number 401905 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• Daig Livewire Steerable, Product Number 401904 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• Daig Livewire Steerable, Product Number 401652 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• Daig Livewire Steerable, Product Number 401603… recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• Daig Livewire Steerable, Product Number 401582 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• Daig Livewire Steerable, Product Number 401581 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• Daig Livewire Steerable, Product Number 401575 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• CS Uni-Directional w Auto ID, Product Number D135304 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• CS Uni-Directional w Auto ID, Product Number D135303 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• BW Webster Duo-Decapolar, Product Number D728260RT recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II
• BARD EP XT Steerable, Product Number 200794 recall
  FDA May 20, 2026 · Stryker Sustainability Solutions · Class II