Medical device recalls (page 2)
2545 recalls.
- Brand Name: VACUETTE Product Name: LH Lithium Heparin Separator Model/Catalog... recall (Greiner Bio-One North America, Inc.)
Medical deviceClass IIReported October 28, 2026 · Lot B26043FM may include EDTA contamination which introduces potassium while chelating calcium in patient samples, leading to falsely elevated potassium (K+)... - Philips Smart-hopping 2.0 AP 1.4 GHz recall (Philips North America)
Medical deviceClass IIReported October 28, 2026 · Unreliable wireless roaming behavior of Smart-hopping 1.0 wireless clients during transport when connecting to Smart-hopping 2.0 infrastructure, resulting in... - Medtronic Biopsy Needle Kit recall (Medtronic Navigation, Inc.)
Medical deviceClass IIReported October 28, 2026 · Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect... - Medtronic NDI Passive Spheres REF: 8801075 recall (Medtronic Navigation, Inc.)
Medical deviceClass IIReported October 28, 2026 · Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect... - Medtronic NDI Passive Spheres REF: 8801074 recall (Medtronic Navigation, Inc.)
Medical deviceClass IIReported October 28, 2026 · Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect... - Medtronic NDI Passive Spheres REF: 8801071 recall (Medtronic Navigation, Inc.)
Medical deviceClass IIReported October 28, 2026 · Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect... - B Braun SAFSITE Injection Site recall (B Braun Medical Inc)
Medical deviceClass IIReported October 28, 2026 · Potential for leakage and backflow at the Safsite valve. - Think Surgical Square Driver REF: 109126 recall (Think Surgical, Inc.)
Medical deviceClass IIReported October 28, 2026 · Robotic system square drive failed to meet design specifications potentially resulting in pin becoming stuck in square driver or the pin wobbling during... - Amplatzer Amulet Left Atrial Appendage Occluder Model Numbers 1. 9-ACP2-007-016 ... recall (Abbott)
Medical deviceClass IIReported October 28, 2026 · Changes to Instructions for Use (IFU) for the device regarding risk of Pulmonary Artery Injury (PAI). - Philips Lumify Diagnostic Ultrasound System recall (Philips Ultrasound, LLC)
Medical deviceClass IReported October 28, 2026 · Ultrasound system may: 1) Not recognize previous transducer registration, prevent scanning, require re-registration with Wi-Fi/cellular access, which may be... - V*Home recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - V+ Pro Emergency recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VC recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VC Model Number: PRT-01098-000 recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - V+Pro Model Number: PRT-01185-000 recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VCSN+Pro Model Number: PRT-01184-000 recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VOCSN recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VOCSN Model Number: PRT-01100-000 recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VC+Pro recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VC+Pro Model Number: PRT-00900-001 recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VOCSN+Pro recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VOCSN+Pro recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists recall (Radiometer Medical ApS)
Medical deviceClass IIReported October 21, 2026 · In vitro diagnostic analyzer had a risk of potentially inaccurate results requiring changes to instructions for use and: 1) Sample types, including whole blood... - Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Discrepancy in the shelf-life of a component - Vinyl Instrument Guards recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported October 21, 2026 · Labeling not compliant with 21 CFR 801 and steam sterilization IFU has been updated. - Scout MD recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported October 21, 2026 · The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use. - IntelePACS recall (INTELERAD MEDICAL SYSTEMS INCORPORATED)
Medical deviceClass IIReported October 21, 2026 · Following a Chromium-based web-browser, report and displayed images may not match. - Convenience Kits containing CONMED AirSeal Access Ports KIT ROBOTICS UROLOGY... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports CHN GYN ONCOLOGY ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports GENERAL DAVINCI ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports HERNANDEZ DAVINCI ACC... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Medline surgical convenience kits labeled as: 1) SPINAL CDS recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: OPEN HEART recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) NEURO-SPINE BASIN PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A & recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) CV BASIN PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) MAIN/LAPAROSCOPY TRANSPLA PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) EAR recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: VEIN HARVESTING PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) VEIN HARVESTING PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - 1) Product Name AUD OPEN HEART PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: CABG AUXILIARY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - TS Misc. Instruments Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - Triathlon Hinge Femoral Prep Tray. Catalog Number: 6543-6-514. recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - TS Femoral Prep Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - TS Universal Baseplate Finishing Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - Williams Cystoscopic Injection Needles recall (Cook Incorporated)
Medical deviceClass IIReported October 21, 2026 · The female Luer lock adapter component in the affected device lots may not have been correctly seated due to misalignment and inadequate torquing during... - LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762. recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIIReported October 21, 2026 · In kit sub-lot 2530M-01 the date of expiration printed on the outer labeling may indicate the wrong expiration date of July 22, 2026 while the correct... - IQ200 SPRINT recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported October 21, 2026 · The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however... - DxU 840m Iris recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported October 21, 2026 · The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however... - MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control recall (Microgenics Corporation)
Medical deviceClass IIReported October 21, 2026 · Vial-to-vial variability in MAS¿ Omni"IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, Lot OPRO29061A results in low Parathyroid Hormone... - Generic Name: GORE VIABIL Short Wire Biliary Endoprosthesis recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported October 21, 2026 · The potential for the devices to be mislabeled with the incorrect length. - REF: P65 ST862 CoLag SCREW recall (In2bones USA, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to labeling error, bone screws specified as fully threaded, are actually partially threaded screws. - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture recall (Ethicon, LLC)
Medical deviceClass IIReported October 21, 2026 · Silk sutures, indicated for use in cardiovascular, ophthalmic and neurological procedures, packaged with alcohol-based fluid, not part of product design, that... - Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 ... recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported October 21, 2026 · Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift... - Generic Name: BioFire¿ Joint Infection recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel... recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - Generic Name: FilmArray¿ Pneumonia Panel Generic Name: FilmArray¿ Pneumonia Panel ... recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - FORWARD Gunshot Wound Kit recall (INTEGRATED MEDCRAFT LLC)
Medical deviceClass IIReported October 21, 2026 · Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device's sterile pad, potentially causing the... - iFuse TORQ Implant System Model/Catalog Number: 10055T recall (SI-BONE, Inc.)
Medical deviceClass IIReported October 21, 2026 · The pelvic fixation screws failed to meet acceptance criteria for tube packaging seal integrity testing; therefore, sterility assurance cannot be ensured. - Power F2 Powered Fastening System recall (Ferno-Washington Inc)
Medical deviceClass IIReported October 21, 2026 · Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system... - Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack recall (Sarnova HC, Llc)
Medical deviceClass IIReported October 21, 2026 · Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula. - NaviFlex LW Pusher recall (Boston Scientific Corporation)
Medical deviceClass IIReported October 21, 2026 · Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this... - NeuroStar Advanced Therapy System. Contains the NeuroStar HP Coil Assembly Part Number... recall (Neuronetics, Inc.)
Medical deviceClass IIReported October 21, 2026 · Cables are not in conformance with the product specifications required in the production of the HP Coil Assembly. - Brand Name: IOMAX Product Name: IOMAX Cortical Module Model/Catalog Number:... recall (Cadwell Industries Inc)
Medical deviceClass IIReported October 21, 2026 · Stimulator device contains a defective printed circuit board assembly (PCBA) that may cause the device to unintentionally deliver electrical stimulation to the... - BD Phoenix Panel NMIC-306. Catalog Number: 449292. recall (Becton Dickinson & Co.)
Medical deviceClass IIReported October 21, 2026 · Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. - BD Phoenix Panel NMIC-312. Catalog Number: 449082. recall (Becton Dickinson & Co.)
Medical deviceClass IIReported October 21, 2026 · Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. - Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined... recall (Medtronic Sofamor Danek USA Inc)
Medical deviceClass IIReported October 21, 2026 · Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to... - Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined... recall (Medtronic Sofamor Danek USA Inc)
Medical deviceClass IIReported October 21, 2026 · Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related... - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - HemoslL AcuStar HIT-lgG recall (Instrumentation Laboratory)
Medical deviceClass IReported October 21, 2026 · Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples. - HemoslL AcuStar HIT-lgG recall (Instrumentation Laboratory)
Medical deviceClass IReported October 21, 2026 · Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples. - Intellijoint Navigation System: Workstation G2 Configured recall (Intellijoint Surgical, Inc.)
Medical deviceClass IIReported October 14, 2026 · A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch MacBook Pro... - HexaVue Focus Integration System recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · A software issue may result in unintended mismatch of patient information on manually printed images. Incorrect patient information appearing on printed images... - TufTex¿ Over-the-Wire Embolectomy Catheter recall (LeMaitre Vascular, Inc.)
Medical deviceClass IIReported October 14, 2026 · Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing. - T1 Patient Monitor. Operator's Manual: T1 Patient Monitor recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12 recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - Passport Series Patient Monitor. Operator's Manuals: 8 / 12 / 12M / 17M / V recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - BeneView Series. Operator's Manuals: T5 / T8 recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - Panorama and Telemetry Monitoring System. Operator's Manuals: TMS-6016/Panorama... recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - BeneVision Series Telemetry Monitor. Operator's Manuals: TM70/TM80 recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - BeneVision N1 and N-Series Patient Monitor. Patient Monitor: N12/N15/N17/N19/N22. recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - ePM Series Patient Monitor. Patient Monitor Series: ePM 10M/ePM 12M/ePM 12MA/ ePM... recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - Alphenix INFX-8000C/B5 recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported October 14, 2026 · Loosening of the bolts securing the longitudinal movement mechanism may cause the tabletop to shift, resulting in [positional/imaging/patient] misalignment and... - SEDIPLAST recall (POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC)
Medical deviceClass IIReported October 14, 2026 · During use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause the tube... - ABD HYSTERECTOMY 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 PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - MAJOR PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - UROLOGY MAJOR recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - HEART PREP TRAY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - DAVINCI LAP/GYN recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - PLASTICS TRAY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process.