July 8, 2026Medical DevicesFDA
RAYSEARCH LABORATORIES AB recalls RayCare 2024A SP1. Oncology Information Systems.
Hazard: Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.
July 8, 2026Medical DevicesFDA
Medela Inc recalls Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog Number: ENF060182LD / 101033086 S
Hazard: May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery of enteral nutritional fluids or oral medication.
July 8, 2026Medical DevicesFDA
Accuray Incorporated recalls Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer; Linear Accelerator
Hazard: In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control pendant, the collimator may release and fall from the housing.
July 8, 2026Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls ARTIS icono floor. Model Number: 11327700.
Hazard: Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
July 8, 2026Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls ARTIS icono ceiling. Model Number: 11328100.
Hazard: Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
July 8, 2026Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls ARTIS icono biplane. Model Number: 11327600.
Hazard: Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
July 8, 2026Medical DevicesFDA
Accuray Incorporated recalls Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer; Linear Accelerator
Hazard: In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control pendant, the collimator may release and fall from the housing.
July 8, 2026Medical DevicesFDA
TELEFLEX LLC recalls Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips
Hazard: Due to out-of-specification, or potential out-of-specification, levels of endotoxins
July 8, 2026Medical DevicesFDA
Baxter Healthcare Corporation recalls Adapter for Head Positioning, Model/Catalog Number: 1739994, when used in conjunction with the side rails of the Upper B
Hazard: The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of the Upper Back Section H V U component on Baxter operating tables.
July 8, 2026Medical DevicesFDA
Boston Scientific Corporation recalls CRE Wireguided 18-20mm 240cm
Hazard: Potential sterile breach of the pouches in which devices are packaged.
July 8, 2026Medical DevicesFDA
Boston Scientific Corporation recalls CRE Wireguided 15-18mm 240cm
Hazard: Potential sterile breach of the pouches in which devices are packaged.
July 8, 2026Medical DevicesFDA
Boston Scientific Corporation recalls CRE Wireguided 12-15mm 240cm
Hazard: Potential sterile breach of the pouches in which devices are packaged.
July 8, 2026Medical DevicesFDA
Boston Scientific Corporation recalls CRE Wireguided 10-12mm 240cm
Hazard: Potential sterile breach of the pouches in which devices are packaged.
July 8, 2026Medical DevicesFDA
Boston Scientific Corporation recalls CRE Wireguided 8-10mm 240cm
Hazard: Potential sterile breach of the pouches in which devices are packaged.
July 8, 2026Medical DevicesFDA
Boston Scientific Corporation recalls CRE Wireguided 6-8mm 240cm
Hazard: Potential sterile breach of the pouches in which devices are packaged.
July 8, 2026Medical DevicesFDA
Boston Scientific Corporation recalls CRE Pro Wireguided 18-20mm 240cm
Hazard: Potential sterile breach of the pouches in which devices are packaged.
July 8, 2026Medical DevicesFDA
Boston Scientific Corporation recalls CRE Pro Wireguided 15-18mm 240cm
Hazard: Potential sterile breach of the pouches in which devices are packaged.
July 8, 2026Medical DevicesFDA
Boston Scientific Corporation recalls CRE Pro Wireguided 12-15mm 240cm
Hazard: Potential sterile breach of the pouches in which devices are packaged.
July 8, 2026Medical DevicesFDA
Boston Scientific Corporation recalls CRE Pro Wireguided 10-12mm 240cm
Hazard: Potential sterile breach of the pouches in which devices are packaged.
July 8, 2026Medical DevicesFDA
Boston Scientific Corporation recalls CRE Pro Wireguided 8-10mm 240cm
Hazard: Potential sterile breach of the pouches in which devices are packaged.
July 8, 2026Medical DevicesFDA
Boston Scientific Corporation recalls CRE Pro Wireguided 6-8mm 240cm
Hazard: Potential sterile breach of the pouches in which devices are packaged.
July 8, 2026Medical DevicesFDA
Hamilton Medical AG recalls IntelliCuff, Portable automatic cuff pressure controller REF: 951001
Hazard: Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the cuff pressure set by the user.
July 8, 2026Medical DevicesFDA
Medtronic Heart Valves Division recalls Medtronic Harmony Delivery Catheter System
Hazard: Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system under certain procedural or anatomical conditions due to a manufacturing issue.
July 8, 2026Medical DevicesFDA
Remel, Inc recalls GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460
Hazard: Reduced or no recovery of some strains of Neisseria gonorrhoeae.
July 8, 2026Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical convenience kit
Hazard: Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
July 8, 2026Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls A M S, ALIGNED MEDICAL SOLUTIONS, Preop Kit-NS, Pack Number AMS18227, surgical convenience kit
Hazard: Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
July 8, 2026Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls A M S, ALIGNED MEDICAL SOLUTIONS, Thyroid FNA Pack-RX, Pack Number AMS17729, surgical convenience kit
Hazard: Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
July 8, 2026Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls A M S, ALIGNED MEDICAL SOLUTIONS, DSAEK Pack-RX, Pack Number AMS12394B, surgical convenience kit
Hazard: Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
July 8, 2026Medical DevicesFDA
Medacta Usa Inc recalls Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970, 8/04.01.10.0971, 9/04.01.10.0972, 10/04.01.10.0973, 11/04.
Hazard: Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the stem reamer are positioned approximately 0.2 mm per size more laterally than intended, which may increase the risk of fracture in the medial region of the proximal humerus.
July 8, 2026Medical DevicesFDA
DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below product descriptions and Part Codes.
Hazard: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.