Medical device recalls (page 19)
2545 recalls.
- Multi-parameter Command Module recall (Spacelabs Healthcare, Inc.)
Medical deviceClass IIReported April 15, 2026 · Multi-parameter command module has a circuit board issue and when in Auto mode, Cardiac Output (CO) measurement may activate early, resulting in Bad Curve... - COOK MEDICAL Wayne Pneumothorax Tray: Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Wayne Pneumothorax Set: Reference Part Number C-UTPT-1020-WAYNE-IMH recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Thal-Quick Chest Tube Tray: Reference Part Number C-TQTSY-3200 recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Spectrum¿ Central Venous Tray: Reference Part Number... recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Spectrum¿ Central Venous Catheter Set: Reference Part Number... recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL NCompass¿ Nitinol Stone Extractor: Reference Part Number C-NTSE-2.4-115-NC3 recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Multipurpose Drainage Catheter: Reference Part Number... recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set: Reference Part Number... recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Cook¿ Strange Bile Duct Stone Exploration Set: Reference Part Number... recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Cook¿ Spectrum¿ Central Venous Catheter Tray: Reference Part Number... recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Cook Staged Extubation Set: Reference Part Number C-CAE-14.0-83-EXTU recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Set: Reference... recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Blue Rhino¿ G2-Multi Percutaneous Tracheostomy Introducer Tray: ... recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set: Reference... recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Arterial Pressure Monitoring Tray recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Approach CTO-18 Micro Wire Guide recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Approach CTO-12 Micro Wire Guide: Reference Part Number CMW-14-190-12G recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - COOK MEDICAL Approach CTO-6 Micro Wire Guide recall (Cook Incorporated)
Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. - See Luer Cap Set recall (Molded Products Inc)
Medical deviceClass IIReported April 15, 2026 · Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve... - XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm recall (XTANT Medical Holdings, Inc)
Medical deviceClass IIReported April 15, 2026 · Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is. - Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat recall (Tornier, Inc)
Medical deviceClass IIReported April 15, 2026 · Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are incompatible with... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - NAMIC Angiographic Syringe recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - NAMIC Angiographic Syringe recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - NAMIC Angiographic Control Syringe recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - NAMIC Angiographic Syringe recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - ARTIS pheno and ARTIS Icono biplane recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported April 15, 2026 · During patient examinations, the system may sporadically display a major increase of the x-ray dose applied to the patient. Despite the reported dose showing... - Cardinal Health Monoject Tuberculin Syringe recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported April 8, 2026 · The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes... - SIGNA Premier systems recall (GE Healthcare LLC)
Medical deviceClass IIReported April 8, 2026 · Whole-Body MR scanners used to produce images of the inside of the human body to aid diagnosis of disease may have been manufactured/serviced with ferrous... - OXOID MICROBACT IDENTIFICATION KITS recall (Oxoid Australia Pty Limited)
Medical deviceClass IIReported April 8, 2026 · Oxoid Ltd., part of Thermo Fisher Scientific, confirmed that Microbact 12L Kit 20 Tests MB1128A lot 4494873 may identify incorrect organism due to... - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Paradigm REAL-Time Veo Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 530G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - Paradigm REAL-Time Revel Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - Paradigm REAL-Time Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - Paradigm Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 620G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 740G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 720G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 700G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 640G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 770G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 780G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 630G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 670G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - eTRAX Needle Sensor - 18G recall (Civco Medical Instruments Co. Inc.)
Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be... - eTRAX Needle Sensor - 16G recall (Civco Medical Instruments Co. Inc.)
Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be... - eTRAX Needle Sensor - 14G recall (Civco Medical Instruments Co. Inc.)
Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be... - eTRAX Needle Sensor - 12G recall (Civco Medical Instruments Co. Inc.)
Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be... - eTRAX Needle System Starter Kit 18G recall (Civco Medical Instruments Co. Inc.)
Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be... - eTRAX Needle System Starter Kit 16G recall (Civco Medical Instruments Co. Inc.)
Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be... - eTRAX Needle System Starter Kit 14G recall (Civco Medical Instruments Co. Inc.)
Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be... - eTRAX Needle System Starter Kit 12G recall (Civco Medical Instruments Co. Inc.)
Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be... - MEDLINE ANTERIOR HIP PACK DYNJ64672B recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Medline kits containing Olympus biopsy valves: 1. BRONCH PROCEDURE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Medline kits containing Olympus biopsy valves: 1. BRONCHOSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Medline kits containing Olympus biopsy valves: 1. BAL KIT recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - THORACIC ROBOTS recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Medline convenience kits containing Olympus biopsy valves: 1. BRONCH PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Airway Exam Kit recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - 2.4 VOLT recall (Synthes (USA) Products LLC)
Medical deviceClass IIReported April 8, 2026 · A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an... - 2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US. recall (Synthes (USA) Products LLC)
Medical deviceClass IIReported April 8, 2026 · A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an... - Brand Name: da Vinci S recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported April 8, 2026 · Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments - Brand Name: da Vinci S recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported April 8, 2026 · Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments - Brand Name: da Vinci S recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported April 8, 2026 · Due to increased complaints for broken/frayed grip cables for reusable instruments. - Brand Name: da Vinci S recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported April 8, 2026 · Due to increased complaints for broken/frayed grip cables for reusable instruments. - Brand Name: da Vinci S recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported April 8, 2026 · Due to increased complaints for broken/frayed grip cables for reusable instruments. - Brand Name: da Vinci S recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported April 8, 2026 · Due to increased complaints for broken/frayed grip cables for reusable instruments. - Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 8, 2026 · Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the... - Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 8, 2026 · Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the... - Sterile Radiology Procedure Kits recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility. - Vue Motion V12. Product Number: 1017979. recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence. - Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT ... recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage....