Medical device recalls (page 8)
2545 recalls.
- Allura Xper FD. Model Numbers: 722026 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported August 19, 2026 · Firmware issue potentially leading to loss of geometry movements. - Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL recall (Remel Europe Ltd.)
Medical deviceClass IIReported August 19, 2026 · Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds. - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623 recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31... recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING ... recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 ... recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP recall (Galt Medical Corporation)
Medical deviceClass IIReported August 19, 2026 · Black depth markings may detach from the outer sheath of the coaxial dilator introducer component of transcarotid-peripheral access kits. - Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 ... recall (Spacelabs Healthcare, Inc.)
Medical deviceClass IIReported August 19, 2026 · Due to off-the-shelf display port component that has audio/video failures - GORE VIABIL Short Wire Biliary Endoprosthesis recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported August 19, 2026 · 10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes... - GORE VIABIL Short Wire Biliary Endoprosthesis recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported August 19, 2026 · 10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes... - navify Digital Pathology recall (Ventana Medical Systems, Inc.)
Medical deviceClass IIReported August 19, 2026 · Due to complaints received for the Image Management System regarding image/metadata discrepancy with the Viewer window - BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL ... recall (MICROVENTION INC.)
Medical deviceClass IIReported August 19, 2026 · Due to an increase rate of balloon pinhole defects. - Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection recall (Spectra Medical Devices, Llc)
Medical deviceClass IReported August 19, 2026 · Manufacturing firm, Huons, was cited for issues regarding product quality and sterility assurance. If the product sterility is compromised, patients may be... - Baxter Duo-Vent Solution Set and Male Luer Lock Adapter recall (Baxter Healthcare Corporation)
Medical deviceClass IReported August 19, 2026 · Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open... - Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated... recall (Contego Medical, Inc)
Medical deviceClass IIReported August 12, 2026 · Carotid stent and post-dilation balloon system with integrated embolic protection system has an integrated filter, that due to a wire-to-filter-bond issue, may... - Blom-Singer Classic Indwelling Voice Prosthesis recall (Freudenberg Medical, LLC)
Medical deviceClass IIReported August 12, 2026 · Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large... - Blom-Singer Classic Indwelling Voice Prosthesis recall (Freudenberg Medical, LLC)
Medical deviceClass IIReported August 12, 2026 · Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM Connect Product Name: COAPTIUM Connect Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - GEM Premier 5000 PAK Part Numbers: 00055360010 00055360011 00055407504 ... recall (Instrumentation Laboratory)
Medical deviceClass IIReported August 12, 2026 · The active ingredient concentration in the lysing bag solution of specific GEM Premier 5000 lots did not meet established manufacturing specifications. The... - GEM Premier 7000 with iQM3 Part Numbers: 00077407508 00077407510 00077415004 ... recall (Instrumentation Laboratory)
Medical deviceClass IIReported August 12, 2026 · The active ingredient concentration in the lysing bag solution of specific GEM Premier 7000 with iQM3 PAK lots did not meet established manufacturing... - Brand Name: U2 Total Knee System Product Name: Femoral offset bushing recall (United Orthopedic Corp.)
Medical deviceClass IIReported August 12, 2026 · Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant. - Brand Name: U2 Total Knee System Product Name: Femoral offset bushing recall (United Orthopedic Corp.)
Medical deviceClass IIReported August 12, 2026 · Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant. - 5-PLASMA Bivalirudin Control recall (Aniara Diagnostica LLC)
Medical deviceClass IIReported August 12, 2026 · Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of... - 5-PLASMA Bivalirudin Calibrator recall (Aniara Diagnostica LLC)
Medical deviceClass IIReported August 12, 2026 · Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of... - 5-PLASMA Bivalirudin AMR Verification Kit recall (Aniara Diagnostica LLC)
Medical deviceClass IIReported August 12, 2026 · Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of... - Philips Allura recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported August 12, 2026 · Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives. - Philips Azurion under the following System Descriptions and corresponding model... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported August 12, 2026 · Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives. - Philips Allura under the following System Descriptions and corresponding model... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported August 12, 2026 · Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives. - Atellica CH Urine Albumin REF: 11537225 recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported August 12, 2026 · Processing of urine albumin assay on the CI analyzers may lead to the following issues: Falsely depressed Atellica CH Urea Nitrogen (UN_c) results; Falsely... - REF # D23354 recall (Beckman Coulter Inc.)
Medical deviceClass IIReported August 12, 2026 · Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications." - REF # D23352 recall (Beckman Coulter Inc.)
Medical deviceClass IIReported August 12, 2026 · Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications." - HardyDisk AST Cefiderocol 30¿g recall (Hardy Diagnostics)
Medical deviceClass IIReported August 12, 2026 · Due to incorrect cartridges include in affected products that there is the potential for false-susceptible or false-resistant susceptibility results and may... - Brand Name: U2 Total Knee System Product Name: Femoral valgus offset adaptor recall (United Orthopedic Corp.)
Medical deviceClass IIReported August 12, 2026 · Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail. - Brand Name: U2 Total Knee System Product Name: Femoral valgus adaptor recall (United Orthopedic Corp.)
Medical deviceClass IIReported August 12, 2026 · Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail. - Brand Name: USTAR II Knee System Product Name: Hinge Box Trial recall (United Orthopedic Corp.)
Medical deviceClass IIReported August 12, 2026 · Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail. - Brand Name: U2 Total Knee System Product Name: PSA Box Trial recall (United Orthopedic Corp.)
Medical deviceClass IIReported August 12, 2026 · Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail. - Syva Emit tox Serum Tricyclic Antidepressant Calibrator/Controls SMN 10445390 ... recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIIReported August 12, 2026 · out-of-specification sodium azide concentration in Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2. While the assay results were not... - Syva Emit Disopyramide Assay Enzyme Immunoassay recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIIReported August 12, 2026 · Out-of-specification sodium azide concentration in Syva Emit Disopyramide Enzyme Immunoassay Calibrator Lot U1. While the assay results were not impacted, the... - INFINION CX LEAD KIT recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IReported August 12, 2026 · Spinal cord stimulation system lead body may be exposed to stress at the anchor site. This may result in high impedance measurements or lead fractures, which... - GE Healthcare Portrait Core Services SW V 1.2.0 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported August 12, 2026 · A software vulnerability may allow unauthorized persons to gain privileged access to the device, which could result in loss of patient monitoring, missed... - FilmArray NGDS Warrior Panel REF NGDS-ASY-0007 UDI-DI code: recall (Biofire Defense)
Medical deviceClass IIReported August 12, 2026 · Firm has identified mismatches between the outbreak strain and the reference strain used in the development of its qualitative, multiplexed, nucleic acid-based... - GE Healthcare MAC VU360 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported August 12, 2026 · Software issue issue with the MAC VU360 v3.0 system. After selecting the order refresh icon, an open preview or review screen might fail to close... - Merge OrthoPACS recall (Merge Healthcare, Inc.)
Medical deviceClass IIReported August 12, 2026 · Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open. - Merge PACS recall (Merge Healthcare, Inc.)
Medical deviceClass IIReported August 12, 2026 · Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open. - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475640 Product... recall (Biomet, Inc.)
Medical deviceClass IIReported August 12, 2026 · Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier... - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635 Product... recall (Biomet, Inc.)
Medical deviceClass IIReported August 12, 2026 · Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier... - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product... recall (Biomet, Inc.)
Medical deviceClass IIReported August 12, 2026 · Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier... - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product... recall (Biomet, Inc.)
Medical deviceClass IIReported August 12, 2026 · Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier... - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product... recall (Biomet, Inc.)
Medical deviceClass IIReported August 12, 2026 · Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier... - STRYKER PKG. recall (Stryker Corporation)
Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - STRYKER PKG. recall (Stryker Corporation)
Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING recall (Stryker Corporation)
Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - STRYKER AHTO TUBE SET WITH TIP PACKAGING recall (Stryker Corporation)
Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - STRYKER AHTO TUBE SET PACKAGING recall (Stryker Corporation)
Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 ... recall (Maquet Critical Care AB)
Medical deviceClass IIReported August 12, 2026 · Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient... - Anti-Torque recall (Innovasis, Inc)
Medical deviceClass IIReported August 12, 2026 · Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque... - Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear... recall (Medical Action Industries, Inc. 306)
Medical deviceClass IIReported August 12, 2026 · Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal. - Brand Name: OXOS Medical recall (Oxos Medical Inc)
Medical deviceClass IIReported August 12, 2026 · Due to a defective circuit board that overheats - munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control... recall (MUNEVO GMBH)
Medical deviceClass IIReported August 12, 2026 · A software issue may cause the wheelchair's driving mechanism to fall out of calibration. When this occurs, the device may experience unexpected steering drift... - Nerivio Infinity. Model/Catalog Number: FGD000100. Software Version: FW Version 4.1.2.0 recall (THERANICA BIOELECTRONICS LTD)
Medical deviceClass IIReported August 12, 2026 · Potential for the batter to have a thermal-runway event during charging, resulting in smoke and odor. - Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software... recall (Copan WASP)
Medical deviceClass IIReported August 12, 2026 · Due to a software issue within the WebApp that potentially prevents the user to overwrite the results. - Brand Name: Quantum Rehab Product Name: Quantum Rival Model/Catalog Number: Quantum... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: 4Front Model/Catalog Number: 4Front ... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Quantum 4Front 2HD Model/Catalog Number:... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Q6 Edge 4 Model/Catalog Number: Q6 Edge 4 ... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Q6 Edge 3 Model/Catalog Number: Q6 Edge 3 ... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Q6 Edge 2.0 recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Quantum 1450 Model/Catalog Number: Quantum... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum rehab Product Name: Q6 Edge 2.0 Model/Catalog Number: Q6 Edge... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Q6 Edge HD Model/Catalog Number: Q6 Edge HD ... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: R-TRAK Model/Catalog Number: R-TRAK ... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Q6 Edge 3 Stretto Model/Catalog Number: Q6... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Quantum Outback Model/Catalog Number:... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number:... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN: Radial... recall (Boston Scientific Corporation)
Medical deviceClass IIReported August 12, 2026 · Potential for breach in sterile barrier of device packaging. - Radial Jaw 4 Large Capacity Biopsy Forceps with the following descriptions and UPN: ... recall (Boston Scientific Corporation)
Medical deviceClass IIReported August 12, 2026 · Potential for breach in sterile barrier of device packaging. - Radial Jaw 4 Standard Capacity Biopsy Forceps with the following descriptions and UPN:... recall (Boston Scientific Corporation)
Medical deviceClass IIReported August 12, 2026 · Potential for breach in sterile barrier of device packaging. - Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the... recall (INTEGRATED MEDCRAFT LLC)
Medical deviceClass IIReported August 12, 2026 · Devices could potentially contain an occluded or partially occluded Guedel Airway tip. - FORWARD Oral Airway Kit recall (INTEGRATED MEDCRAFT LLC)
Medical deviceClass IIReported August 12, 2026 · Devices could potentially contain an occluded or partially occluded Guedel Airway tip. - Charger for the Therabody Theragun recall (Therabody, Inc)
Medical deviceClass IIReported August 12, 2026 · Charging cradle for the device may overheat while charging the device's removable battery pack, presenting risk of thermal event (fire). Firm has received... - REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand... recall (Beckman Coulter Biomedical GmbH)
Medical deviceClass IIReported August 12, 2026 · Due to software issues where does not handle combo assay results. The software may replace the final combo test result with one of the sub-results resulting... - Halyard convenience kits containing recalled Medline Namic Angiographic Star Off... recall (AVID Medical, Inc.)
Medical deviceClass IReported August 12, 2026 · Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within... - Halyard convenience kits containing recalled Medline Namic Angiographic Star Off... recall (AVID Medical, Inc.)
Medical deviceClass IReported August 12, 2026 · Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within... - Halyard convenience kits containing recalled Medline Namic Angiographic Star Off... recall (AVID Medical, Inc.)
Medical deviceClass IReported August 12, 2026 · Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within... - Stryker Hoffmann II Connecting Rod Micro 3 x 150mm. Catalog Number: 50796150. recall (Stryker GmbH)
Medical deviceClass IIReported August 5, 2026 · Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Stryker Hoffmann II Connecting Rod Micro 3 x 120mm. Catalog Number: 50796120. recall (Stryker GmbH)
Medical deviceClass IIReported August 5, 2026 · Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Stryker Hoffmann II Connecting Rod Micro 3 x 90mm. Catalog Number: 50796090. recall (Stryker GmbH)
Medical deviceClass IIReported August 5, 2026 · Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. - Stryker Hoffmann II Connecting Rod Micro 3 x 60mm. Catalog Number: 50796060. recall (Stryker GmbH)
Medical deviceClass IIReported August 5, 2026 · Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.