Medical device recalls (page 20)
2545 recalls.
- ENFIT G-TUBE CONNECTOR 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.... - Jiffy Original Composite Polisher Cups recall (Ultradent Products, Inc.)
Medical deviceClass IIReported April 8, 2026 · Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment. - Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001 recall (Stryker Communications)
Medical deviceClass IIReported April 8, 2026 · Surgical light assembly may not adequate support the weight of the ceiling cover. - Artoura Breast Tissue Expanders Reference Numbers:... recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - Artoura Breast Tissue Expanders Reference Numbers:... recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - Artoura Breast Tissue Expanders Reference Numbers:... recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-113TH recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-157LH ... recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113 recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - Azurion 5 M20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 5 M12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 7 M20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 7 M12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 7 B20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 7 B12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 3 M15 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 3 M12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Allura Xper FD20/15 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Allura Xper FD20/15 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Allura Xper FD20/20 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Allura Xper FD20/20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Allura Xper FD20/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD10 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD20 Biplane OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD20 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD20 Biplane recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD10F recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Allura Xper FD10C recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - BD Kiestra" ReadA recall (BD KIESTRA LAB AUTOMATION)
Medical deviceClass IIReported April 8, 2026 · In certain situations, following a system reboot, one or more modules may have become unreachable via the remote connectivity interface. When this occurred... - Atellica CH Enzymatic Hemoglobin A1c recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported April 8, 2026 · A potential for depressed results for Atellica CH A1c_E when processing Atellica CH RCRP on the same analyzer. Customers processing A1c_E and RCRP on separate... - RefleXion X1 Radiotherapy System Model RXM1000 recall (Reflexion Medical, Inc.)
Medical deviceClass IIReported April 8, 2026 · Due to a radiotherapy medical system software defect, when performing angular roll corrections followed by a repeat localization, the roll corrections applied... - Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿... recall (ReCor Medical Inc.)
Medical deviceClass IIReported April 8, 2026 · Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use. - Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿... recall (ReCor Medical Inc.)
Medical deviceClass IIReported April 8, 2026 · Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use. - Philips Respironics Trilogy Evo Universal recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths. - Philips Respironics Trilogy EV300 recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths. - Philips Respironics Trilogy Evo O2 recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths. - Philips Respironics Trilogy Evo recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths. - Blue Ventilator Adapter Module recall (Baxter Healthcare Corporation)
Medical deviceClass IReported April 8, 2026 · Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of a possible... - Automated Impella Controller recall (Abiomed, Inc.)
Medical deviceClass IReported April 8, 2026 · Potential that the "Purge System Blocked" alarm display on the Automated Impella Controller (AIC) could be delayed when using first generation Impella 5.5... - Purge Cassette recall (Abiomed, Inc.)
Medical deviceClass IReported April 8, 2026 · Increased risk of purge leaks with Generation 1 purge cassettes. - Embrace Drill Tower recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported April 1, 2026 · The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the... - Embrace Drill Tower recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported April 1, 2026 · The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the... - Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING recall (Medline Industries, LP)
Medical deviceClass IIReported April 1, 2026 · Elevated endotoxin levels identified in affected lots. Issue may elicit strong inflammatory response if used, including local tissue irritation, delayed wound... - BD Alaris" System with Guardrails" Suite MX with Point of Care Unit recall (CareFusion 303, Inc.)
Medical deviceClass IIReported April 1, 2026 · Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi... - Brand Name: Olympus PKS Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus PKS Cutting Forceps w/Cord recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus PKS Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus HALO PKS Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus PK Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus Everest Bipolar Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Tandem pumps are battery-operated infusion pumps capable of both basal and bolus... recall (Tandem Diabetes Care, Inc.)
Medical deviceClass IIReported April 1, 2026 · The Czech language user guide contained multiple translation errors. The most significant error was that it incorrectly instructs users to verify that the... - MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61 recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 1, 2026 · Three software defects (Pump Error 53, BG check, and Critical Pump Error (Open Book Image)) that occurred as a result of software updates (versions 6.60, 6.61... - Brand Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Product Name:... recall (AMO Puerto Rico Manufacturing, Inc.)
Medical deviceClass IIReported April 1, 2026 · Due to identifying a limited quantity of intraocular lenses that may have a haptic that sticks to the optic which prevents the lens from unfolding as... - Custom Abutment AS Ti recall (Straumann USA LLC)
Medical deviceClass IIReported April 1, 2026 · A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 /... - Custom Abutment Ti recall (Straumann USA LLC)
Medical deviceClass IIReported April 1, 2026 · A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 /... - Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler recall (Koven Technology, Inc.)
Medical deviceClass IIReported April 1, 2026 · Product labeling includes a fetal indication for use that is not cleared under its 510(k). - Drill Plate recall (Orthalign, Inc)
Medical deviceClass IIReported April 1, 2026 · Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm) - Drill Plate recall (Orthalign, Inc)
Medical deviceClass IIReported April 1, 2026 · Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm) - Philips Respironics Trilogy Evo Universal recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 1, 2026 · Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by... - Philips Respironics Trilogy EV300 recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 1, 2026 · Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by... - Philips Respironics Trilogy Evo O2 recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 1, 2026 · Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by... - Philips Respironics Trilogy Evo recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 1, 2026 · Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by... - Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Brand Name: I.T.S. Pelvic Reconstruction System recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - HLS - Hand Locking Plates System with the below descriptions and corresponding article... recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - HCS - Headless Compression Screw System recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - FLS - Foot Locking Plates System and HOL - Hallux Osteotomy Locking Plate with the... recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - I.T.S. DUL recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - I.T.S. LRS recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - Distal Humeral Plates with Angular Stability with the below descriptions and... recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - I.T.S. Fibula Plate PROlock with Angular Stability with the below descriptions and... recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - Pelvic Reconstruction System recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - I.T.S. Screw System with the below descriptions and corresponding article numbers. ... recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - I.T.S. Straight Plate with Angular Stability with the below descriptions and... recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - Olecranonplate with Angular Stability with the below descriptions and corresponding... recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - Pilonplate with Angular Stability recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - FR.O.H. Calcaneus Repair System with the following description: Anterolateral... recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - Brand Name: Humeral Head Plate with Angular Stability recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - Claviculaplate with Angular Stability recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - Volar Radius Plate with Angular Stability with the following description: Radius Plate... recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - Imactis CT-Navigation System recall (GE Medical Systems, LLC)
Medical deviceClass IIReported April 1, 2026 · There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position. - Handy Solutions Neck & Shoulders Heating Pad recall (Navajo Manufacturing Company)
Medical deviceClass IReported April 1, 2026 · If heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by placing pad... - BioFlo DuraMax Catheter recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - DuraMax Chronic Hemodialysis Catheter recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - 16F Dual Valved Splittable Sheath Introducer recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - ProGuide Chronic Dialysis Catheters recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - CentrosFLO Hemodialysis Catheters recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - Flexible Cryoprobe recall (Erbe USA Inc)
Medical deviceClass IReported April 1, 2026 · Probes may rupture/burst during activation - Flexible Cryoprobe recall (Erbe USA Inc)
Medical deviceClass IReported April 1, 2026 · Probes may rupture/burst during activation - Flexible Cryoprobe recall (Erbe USA Inc)
Medical deviceClass IReported April 1, 2026 · Probes may rupture/burst during activation - Battery Charging Station recall (Datascope Corp.)
Medical deviceClass IIIReported March 25, 2026 · The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to ... - Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number:... recall (Hologic, Inc.)
Medical deviceClass IIReported March 25, 2026 · Due to product exhibiting potential to generate either invalid or false negative results.