Medical Device Recalls | FDA Device Safety Alerts And Recall Notices

Medical Device Recall Alerts List

Showing 926 - 950 of 1,678 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. NON VASCULAR PACK, Medline SKU # DYNJ68037C; 2. VEIN, Medline SKU # DYNJ89845; 3. VEIN, Medline SKU # DYNJ89845A. Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.	FDA Z-1719-2026	Medical Device	High	Apr 15, 2026 Recall: Feb 27, 2026	Details
XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL. Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.	FDA Z-1773-2026	Medical Device	High	Apr 15, 2026 Recall: Feb 18, 2026	Details
ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1661-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777 The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes contained within the packages are U-100 Insulin syringes.	FDA Z-1768-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 27, 2026	Details
MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782) 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 insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.	FDA Z-1739-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 13, 2026	Details
Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1675-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US. 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 incorrect thread.	FDA Z-1703-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 25, 2026	Details
Allura Xper FD10C; System Code: 722001; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1659-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
MEDLINE ANTERIOR HIP PACK DYNJ64672B Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.	FDA Z-1711-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 16, 2026	Details
MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851) 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 insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.	FDA Z-1744-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 13, 2026	Details
Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervation Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.	FDA Z-1654-2026	Medical Device	High	Apr 8, 2026 Recall: Jan 29, 2026	Details
Vue Motion V12. Product Number: 1017979. Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.	FDA Z-1692-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 5, 2026	Details
Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only); Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1678-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1663-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
Burlington Medical, BAT (Breast, Axilla and Thyroid) Coverage. Potential for attenuation degradation over time, decreasing the lifespan.	FDA Z-1758-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 11, 2026	Details
Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microw Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments	FDA Z-1700-2026	Medical Device	High	Apr 8, 2026 Recall: Dec 9, 2025	Details
Burlington Medical, Kilt Potential for attenuation degradation over time, decreasing the lifespan.	FDA Z-1755-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 11, 2026	Details
Allura Xper FD20/20; System Code: 722038; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1669-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
Allura Xper FD20/15; System Code: 722058; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1671-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device. In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.	FDA Z-1646-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 2, 2026	Details
Burlington Medical, Caps. Potential for attenuation degradation over time, decreasing the lifespan.	FDA Z-1760-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 11, 2026	Details
Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915 Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.	FDA Z-1708-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 16, 2026	Details
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001 Surgical light assembly may not adequate support the weight of the ceiling cover.	FDA Z-1688-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 23, 2026	Details
ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1667-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
Burlington Medical, Thyroid Shield. Potential for attenuation degradation over time, decreasing the lifespan.	FDA Z-1753-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 11, 2026	Details

Showing 926 - 950 of 1,678 product recalls

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Medical Device Recalls Today

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