Medical device recalls (page 3)
2545 recalls.
- LAPAROSCOPIC PROSTATECTOMY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - ROBOTIC PROSTATECTOMY PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - PACK OPEN HEART CFH recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - CRANIOTOMY PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - ENDOVASCULAR PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - ADULT HEART TRAY SHANDS JACKS recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - GYN LAPAROSCOPY/LAPAROTOMY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - DAVINCI TRUCUSTOM BUNDLE recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - Onkos Surgical Inc. My3D Personalized Pelvic Implant recall (Onkos Surgical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers. - Onkos Surgical Inc. My3D Personalized Pelvic Implant recall (Onkos Surgical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers. - Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station recall (Nihon Kohden America LLC)
Medical deviceClass IIReported October 14, 2026 · Due to a cybersecurity issue associate with a NULL Pointer Dereferences vulnerabiity. If exploited would potentially cause disruption of the centralized... - Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog... recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported October 14, 2026 · Some MiniMed Flex insulin pumps were released with missing (i.e., devices with no result or abort test results are presumed to have failed) or failed... - Rollator recall (Medline Industries, LP)
Medical deviceClass IIReported October 14, 2026 · The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from the rollator... - Rollator recall (Medline Industries, LP)
Medical deviceClass IIReported October 14, 2026 · The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from the rollator... - BARD EP XT DECAPOLAR STEERABLE recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported October 14, 2026 · Diagnostic electrophysiology (EP) catheter may have a breached sterile barrier on the straight seal side of the primary pouch, which if used could lead to... - DxC 500 AU Clinical Chemistry Analyzers: 1. AU w/out ISE recall (Beckman Coulter Inc.)
Medical deviceClass IIReported October 14, 2026 · Beckman Coulter has identified a software issue affecting DxC 500 AU Clinical Analyzers when testing plasma samples. Following user configuration of a Clinical... - DxC 500i Clinical Analyzer Modules: 1. DxC 500 AU Module w/ISE recall (Beckman Coulter Inc.)
Medical deviceClass IIReported October 14, 2026 · Beckman Coulter has identified a software issue affecting DxC 500i Clinical Analyzers when testing plasma samples. Following user configuration of a Clinical... - Sperm Ab ELISA recall (DRG International, Inc.)
Medical deviceClass IIReported October 14, 2026 · Potential for false negative patient results. - Battle Bandage recall (Safeguard US Operating LLC)
Medical deviceClass IIReported October 14, 2026 · Compression bandage may be degraded, which may cause unwanted foreign material to be introduced inside the wound, which may lead to wound exploration and... - Glypto Device recall (Limitless Cryo Spa LLC)
Medical deviceClass IIReported October 14, 2026 · Lack of 510(k) clearance. - Presource Packs containing Medtronic Microstream Components: Intubation Kit ... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported October 14, 2026 · Kits contain Microstream components. Medtronic issued an update to the Instructions for Use of these components due reports of difficulty in disconnecting the... - Spectral CT and Spectral CT 7500 RT recall (PHILIPS MEDICAL SYSTEMS)
Medical deviceClass IIReported October 14, 2026 · Software issues may affect the safety and performance of Spectral CT system(s). The issues may result in image artifacts, wrong slice thickness, or unintended... - HALYARD Laparoscopy Comprehensive Pack II REF: 49332 recall (GRI Medical & Electronic Technology Co., Ltd.)
Medical deviceClass IIReported October 14, 2026 · Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter - Brand Name: ADAPTABLE Beach Chair Product Name: Beach Chair surgical patient... recall (QUANTUM OPS Inc)
Medical deviceClass IIReported October 14, 2026 · Due to a manufacturing issue (inadequate weld) for patient head positioning system. - VERIFY Biological Steam Test Pack Model/Catalog Number: S3069 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Biological Steam Test Pack Model/Catalog Number: S3065 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB006 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - Generic Name: Kit recall (Medical Action Industries, Inc. 306)
Medical deviceClass IIIReported October 14, 2026 · An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027. - Atellica CH Revised C-Reactive Protein recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported October 7, 2026 · The potential for falsely elevated results. - CHARLOTTE CLAW Screw recall (Wright Medical Technology, Inc.)
Medical deviceClass IIReported October 7, 2026 · Screws, intended for use with polyaxial compression plating system intended for foot osteotomies, was manufactured with missing threads on the screwheads... - HOPKINS Telescope 30¿ recall (Karl Storz Endoscopy)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect inside packaging label for eyepiece. - Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER... recall (Beckman Coulter Mishima K.K.)
Medical deviceClass IIReported October 7, 2026 · Certain AU480 chemistry analyzers, with Windows 10 IoT Enterprise 2021 LTSC PCs, may output the message System Stopped By Fatal Error: DBConnectionError... - Brand Name: Penumbra System recall (Penumbra Inc.)
Medical deviceClass IIReported October 7, 2026 · Due to manufacturing issues reperfusion catheters may fracture. - Brand Name: Tandem t:slim mobile application Product Name: t:slim Mobile Application recall (Tandem Diabetes Care, Inc.)
Medical deviceClass IIReported October 7, 2026 · A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a software issue preventing successful pairing of the t:slim application... - Olympus Tripp-Lite P580-025 25ft DisplayPort Cable recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported October 7, 2026 · While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable. - Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger... recall (SPECTRUM MEDICAL SRL)
Medical deviceClass IIReported October 7, 2026 · Due to blood-to-glycol leak in the heat exchanger. - Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger... recall (SPECTRUM MEDICAL SRL)
Medical deviceClass IIReported October 7, 2026 · Due to blood-to-glycol leak in the heat exchanger. - Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code:... recall (Micro Therapeutics, Inc.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect label/product dimensions. Product is supposed to be 3.00 mm in diameter, but unit is packaging was a 2.50 mm in diameter. - Intrapulmonary Percussive Ventilation recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - Travel Air recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - Impulsator recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - Intrapulmonary Percussive Ventilation recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - Intrapulmonary Percussive Ventilation recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - In-Line Valve recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - Intrapulmonary Percussive Ventilation recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - Evolution upgrade 1.5T amd Evolution upgrade 3.0T recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Upgrade to MR 7700 recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Upgrade dStream recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - SmartPath to MR 7700 recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - SmartPath to dStream for 1.5T recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - MR 7700 recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - MR 5300 recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia Elition S and Ingenia Elition X. recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia Ambition S and Ingenia Ambition X. recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia 3.0T and 3.0T CX recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia 1.5T recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia Blue Seal SE and Blue Seal XE recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - NOxBOXi Nitric Oxide Delivery System. Model Number: NOXBOX-I. recall (NOXBOX LTD)
Medical deviceClass IIReported October 7, 2026 · Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxygen sensors. - Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported October 7, 2026 · Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformations, and blood vessels may have holes in packaging that may affect the... - PALACOS MV pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported October 7, 2026 · Potential for monomer liquid leakage. - PALACOS MV+G pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported October 7, 2026 · Potential for monomer liquid leakage. - PALACOS R+G pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported October 7, 2026 · Potential for monomer liquid leakage. - PALACOS R pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported October 7, 2026 · Potential for monomer liquid leakage. - Olympus M3 Gold Autoclavable Lateral Telescope 70. Model Number: M3-70A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported October 7, 2026 · There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the... - Olympus M3 Gold Autoclavable Foroblique Telescope 30. Model Number: M3-30A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported October 7, 2026 · There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the... - Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported October 7, 2026 · The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece... - Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported October 7, 2026 · The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece... - Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported October 7, 2026 · The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece... - Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported October 7, 2026 · The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece... - Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary... recall (American Contract Systems Inc)
Medical deviceClass IIReported October 7, 2026 · Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the... - Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary... recall (American Contract Systems Inc)
Medical deviceClass IIReported October 7, 2026 · Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the... - Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary... recall (American Contract Systems Inc)
Medical deviceClass IIReported October 7, 2026 · Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the... - Brand Name: Opportunity Pro Product Name: Opportunity Pro Model/Catalog Number: 72-50800 recall (American Nitrile Operations Llc)
Medical deviceClass IIReported October 7, 2026 · Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to... - Brand Name: Opportunity Flex Product Name: Opportunity Flex Model/Catalog Number:... recall (American Nitrile Operations Llc)
Medical deviceClass IIReported October 7, 2026 · Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to... - Brand Name: Performance Pro Product Name: Performance Pro Model/Catalog Number:... recall (American Nitrile Operations Llc)
Medical deviceClass IIReported October 7, 2026 · Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to... - Positron Emission Tomography and Computed Tomography System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Positron Emission Tomography and Computed Tomography System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Positron Emission Tomography and Computed Tomography System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Positron Emission Tomography and Computed Tomography System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Positron Emission Tomography and Computed Tomography System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Positron Emission Tomography and Computed Tomography System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Computed Tomography X-ray System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Computed Tomography X-ray System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Computed Tomography X-ray System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Computed Tomography X-ray System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Computed Tomography X-ray System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Computed Tomography X-ray System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v recall (Volcano Corp)
Medical deviceClass IIReported October 7, 2026 · Software system may associate image data from one patient with another patient's record, potentially resulting in incorrect diagnosis or treatment. - EnCor EnCompass Breast Biopsy and Tissue Removal System Console recall (Bard Peripheral Vascular Inc)
Medical deviceClass IIReported October 7, 2026 · Breast biopsy and tissue removal system may experience the following errors: 1) Probe calibration and /or handheld driver failure (code HH01-00020009) , 2) ... - Fisher Scientific Sure-Vue Urine hCG recall (Alere San Diego, Inc.)
Medical deviceClass IIReported October 7, 2026 · hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result. - Fisher Scientific Sure-Vue Urine hCG Strip recall (Alere San Diego, Inc.)
Medical deviceClass IIReported October 7, 2026 · hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result. - Fisher Scientific Sure-Vue Serum/Urine hCG recall (Alere San Diego, Inc.)
Medical deviceClass IIReported October 7, 2026 · hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result. - McKesson CONSULT hCG Urine Cassette recall (Alere San Diego, Inc.)
Medical deviceClass IIReported October 7, 2026 · hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result. - HeartSine samaritan PAD recall (HeartSine Technologies Ltd)
Medical deviceClass IIIReported October 7, 2026 · Products were distributed without the required Maintenance Supplement, which describes an extra check every 3 months in addition to the monthly check. - VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable... recall (Draeger, Inc.)
Medical deviceClass IReported October 7, 2026 · Potential cracks in the hose, which could lead to leakage or the hose falling off. - Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED recall (Medline Industries, LP)
Medical deviceClass IReported October 7, 2026 · Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially... - Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories recall (Medline Industries, LP)
Medical deviceClass IReported October 7, 2026 · Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially...