Medical device recalls (page 10)
2545 recalls.
- Optima XR200amx recall (GE Medical Systems, LLC)
Medical deviceClass IIReported July 22, 2026 · GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety... - Rapid Refill Continuous Injection System recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 22, 2026 · Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the... - ICU Medical Plum Solo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported July 22, 2026 · In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at... - ICU Medical Plum Duo Infusion Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported July 22, 2026 · In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at... - Olympus Glass Body for 194 Ellik Evacuator. Model Number: 190A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Ellik Evacuator Includes Glass Body recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Toomey Evacuator 50cc with Adaptor. Model Number: 188A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Bone Marrow Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - Arterial Line Kit 20ga x 6 recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - T-Lok Bone Marrow Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - General Biospy Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - One-Piece Introducer Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - ABIOMED Intro Kit recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Insertion Kit recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Smart Assist Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella 5.5 SmartAssist S2 Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella 5.5 Smart Assist Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Introducer Kit 14 Fr recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Introducer Kit 14 Fr recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Introducer Kit 23 Fr recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Introducer Kit 14 Fr recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella RP Flex with SmartAssist Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - Abiomed REF: 0052-3006 recall (Oscor Inc.)
Medical deviceClass IReported July 22, 2026 · Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub... - Abiomed REF: 0052-3021 recall (Oscor Inc.)
Medical deviceClass IReported July 22, 2026 · Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub... - Abiomed REF: 0052-3025 recall (Oscor Inc.)
Medical deviceClass IReported July 22, 2026 · Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub... - Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US ... recall (CMR SURGICAL LIMITED)
Medical deviceClass IIReported July 15, 2026 · Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk. - TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia... recall (Think Surgical, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array. - VITEK 2 AST-N447 TEST KIT Product reference 424620 recall (Biomerieux Inc)
Medical deviceClass IIReported July 15, 2026 · Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures. - OmniTract Surgical Retractor System recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported July 15, 2026 · The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be... - GSP Neonatal GALT Kit. Product Codes: 3303-001U recall (WALLAC OY)
Medical deviceClass IIReported July 15, 2026 · Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient... - Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The... recall (Elekta, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. - Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator ... recall (Elekta, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. - Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote... recall (Elekta, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. - Atellica CH Enzymatic Hemoglobin A1c recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported July 15, 2026 · The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely... - 5008X Blood Tubing Set recall (Fresenius Medical Care Holdings, Inc.)
Medical deviceClass IIReported July 15, 2026 · Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X... - Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS recall (Encore Medical, LP)
Medical deviceClass IIReported July 15, 2026 · Due to packaging discrepancy with incorrect product size mixed up. - Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS recall (Encore Medical, LP)
Medical deviceClass IIReported July 15, 2026 · Due to packaging discrepancy with incorrect product size mixed up. - KL Owen Custom Orthodontic Solution recall (Klowen Braces)
Medical deviceClass IIReported July 15, 2026 · A product error defect may cause incorrect bracket placement. - MiniMed 780G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported July 15, 2026 · A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and... - Medline Convenience Kits: 1) OPEN HEART PEDS PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the... - Medline Convenience Kits: 1) OPEN HEART PEDS PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the... - Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the... - Intracept Access Instruments recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported July 15, 2026 · Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if... - Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in. recall (ConvaTec, Inc)
Medical deviceClass IIReported July 15, 2026 · Surgical dressing manufactured out of specification (greater thickness). - Olympus Single Use Distal Cover recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 15, 2026 · Olympus has developed and released newly designed version of the Distal Cover (MAJ-2315) to replace previous design of the Single Use Distal Covers. - Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems... recall (Zimmer Surgical Inc)
Medical deviceClass IIReported July 8, 2026 · Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result... - Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems... recall (Zimmer Surgical Inc)
Medical deviceClass IIReported July 8, 2026 · Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result... - GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to catheter separation - Radius VSM Disposable NIBP Cuff recall (Masimo Corporation)
Medical deviceClass IIReported July 8, 2026 · Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on... - Radius VSM ECG pre-connected Set recall (Masimo Corporation)
Medical deviceClass IIReported July 8, 2026 · Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on... - Solar GI System recall (Laborie Medical Technologies Corp)
Medical deviceClass IIReported July 8, 2026 · Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's... - 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOFT... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035258 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236129... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code:... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - OTP5000 THORA/PARA TRAY recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number:... recall (BD SWITZERLAND SARL)
Medical deviceClass IIReported July 8, 2026 · Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market. - Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 ... recall (Covidien LLC)
Medical deviceClass IIReported July 8, 2026 · Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP. - Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557 recall (Carl Zeiss Meditec AG)
Medical deviceClass IIReported July 8, 2026 · Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications. - ARTIS icono ceiling. Model Number: 11328100. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential issue with the Display ceiling suspension (DCS Fix XL) that holds the monitor in place. Over time some screws that keep the monitor attached to the... - RayCare 2024A SP4. Oncology Information Systems. recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported July 8, 2026 · Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during... - RayCare 2024A SP1. Oncology Information Systems. recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported July 8, 2026 · Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during... - Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog... recall (Medela Inc)
Medical deviceClass IIReported July 8, 2026 · May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery... - Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer recall (Accuray Incorporated)
Medical deviceClass IIReported July 8, 2026 · In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the... - ARTIS icono floor. Model Number: 11327700. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - ARTIS icono ceiling. Model Number: 11328100. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - ARTIS icono biplane. Model Number: 11327600. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer recall (Accuray Incorporated)
Medical deviceClass IIReported July 8, 2026 · In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the... - Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges recall (TELEFLEX LLC)
Medical deviceClass IIReported July 8, 2026 · Due to out-of-specification, or potential out-of-specification, levels of endotoxins - Adapter for Head Positioning recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported July 8, 2026 · The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of... - CRE Wireguided 18-20mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 15-18mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 12-15mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 10-12mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 8-10mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 6-8mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 18-20mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 15-18mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 12-15mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 10-12mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 8-10mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 6-8mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - IntelliCuff recall (Hamilton Medical AG)
Medical deviceClass IIReported July 8, 2026 · Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the... - Medtronic Harmony Delivery Catheter System recall (Medtronic Heart Valves Division)
Medical deviceClass IReported July 8, 2026 · Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system... - GC Agar Base recall (Remel, Inc)
Medical deviceClass IIReported July 8, 2026 · Reduced or no recovery of some strains of Neisseria gonorrhoeae. - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a...