Recalls in Indiana (page 16)
4018 recalls.
- 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 - 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... - 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. - 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... - 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... - 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 - Short Monobloc Stem Broaches recall (Medacta Usa Inc)
Medical deviceClass IIReported July 8, 2026 · Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the... - Breathing circuit set recall (Hamilton Medical AG)
Medical deviceClass IReported July 8, 2026 · Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test, which... - a.) nara organics brand recall (NARA ORGANICS INC)
FoodClass IReported July 8, 2026 · Product may be contaminated with Clostridium botulinum. - MOGO PURE MORINGA OLEIFERA CAPSULES recall (MOGO Moringa LLC)
FoodClass IReported July 8, 2026 · Product may be contaminated with Salmonella Typhimurium - Glucagon Emergency Kit for Low Blood Sugar recall (Lupin Pharmaceuticals Inc.)
DrugClass IIReported July 8, 2026 · CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing. - Gemcitabine Injection recall (McKesson)
DrugClass IIReported July 8, 2026 · Temperature Abuse: Product was stored incorrectly in a controlled room temperature environment instead of a refrigerated environment. - Revitaderm Wound Care recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated - Fungal Fusion ERADICATION Solution recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - TERPENICOL Antifungal Solution recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - vite20 Antifungal Cream recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - TERPENICOL Antifungal Cream recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - TRIPENICOL S Antifungal Solution recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - TRIFLUENT PHARMA TRIDERGEL Wound Care Gel recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated - Revitaderm Wound Care Gel recall (Blaine Labs Inc)
DrugClass IReported July 8, 2026 · Microbial contamination of Non-Sterile Product: samples identified the presence of Lysinibacillus fusiformis and other Bacillus spp - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported July 8, 2026 · cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported July 8, 2026 · cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported July 8, 2026 · cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). - Dextroamphetamine Saccharate recall (Lannett Company Inc.)
DrugClass IIReported July 8, 2026 · Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules. - Lidocaine HCl Injection USP recall (Asclemed USA Inc.)
DrugClass IIReported July 8, 2026 · Lack of Assurance of Sterility - Accucaine recall (Asclemed USA Inc.)
DrugClass IIReported July 8, 2026 · Lack of Assurance of Sterility - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported July 8, 2026 · Subpotent Drug - prednisoLONE Acetate Ophthalmic Suspension recall (Lupin Pharmaceuticals Inc.)
DrugClass IIReported July 8, 2026 · Presence of Foreign Substance - Fexofenadine Hydrochloride Tablets recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported July 8, 2026 · Failed Impurities/Degradation Specifications - IMULDOSA recall (ACCORD BIOPHARMA INC)
DrugClass IIReported July 8, 2026 · Lack of assurance of Sterility: - BD ChloraPrep CLear recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep CLear recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Scrub Teal recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Scrub Teal recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Hi-Lite Orange recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Hi-Lite Orange recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - ChloraPrep FREPP recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD PurPrep recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Hi-Lite Orange recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - 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... - 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... - 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. - 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... - 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... - 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... - 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... - 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... - 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... - Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH recall (Medline Industries, LP)
Medical deviceClass IReported July 8, 2026 · Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on... - Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A CDS ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters CV ANESTHESIA -... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters CENTRAL AND... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC MAJOR ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Omnipod recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Omnipod DASH Pod. Includes the below Model/REF Numbers: 1. POD-BLE-I1-525 recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Omnipod 5 Pods. Includes the below Model/REF Numbers: 1. POD-OMNI-I1-6720. 2.... recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Hillrom VOLARA System P.CIRCUIT 5KIT AC recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA System P.CIRCUIT KIT AC recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an...