Recalls in Georgia (page 30)
4046 recalls.
- 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... - Muscccm Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by SZ Hengxun
Consumer productReported April 10, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and... - Prestige Import Group Recalls Supernova and Typhoon Lighters Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Cigarette Lighters
Consumer productReported April 10, 2026 · The recalled lighters violate the mandatory standard for cigarette lighters because they do not have the required child-resistant mechanism, posing a risk of... - LED Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries; Sold on Amazon by Happiness Light
Consumer productReported April 10, 2026 · The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain lithium coin... - Shenzhen Shijingjie Network Technology Male-to-Male Extension Cords Recalled Due to Risk of Serious Injury and Death from Electrocution and Carbon Monoxide Poisoning Hazards; Sold on Walmart
Consumer productReported April 10, 2026 · The recalled male-to-male extension cords violate safety requirements because their exposed prongs can become energized when one end is plugged into a... - Shenzhen Baihang Recalls VEEKTOMX Mini Power Banks, Due to Fire and Burn Hazards; Sold on Amazon
Consumer productReported April 10, 2026 · The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers. - ShymeryDirect LED Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries
Consumer productReported April 10, 2026 · The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain lithium coin... - Yeeluzan Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Yeeluzan
Consumer productReported April 10, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and... - Halloween Pumpkin Carving Kits Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries; Sold on Amazon by Besslly Store
Consumer productReported April 10, 2026 · The recalled carving kits violate the mandatory standard for consumer products with button cell and coin batteries because the button cell batteries in the tea... - Head USA Recalls Ski Boots Due to Risk of Serious Injury from Fall Hazard
Consumer productReported April 10, 2026 · The fluorescent yellow materials of the boot shell and sole inserts can deteriorate and break, posing a risk of serious injury from a fall. - Seasonal Specialties Recalls Members Mark 7' Pre-Lit Twinkling Bucks Due to Burn Hazard
Consumer productReported April 10, 2026 · If the wires are connected incorrectly, the current limiting resistor can overheat, posing a burn hazard. - SCUBAPRO Recalls Monorail Weight Pockets for Buoyancy Compensator Devices (BCDs) Due to Risk of Serious Injury or Death from Drowning
Consumer productReported April 10, 2026 · The D-ring handle that is used to unlock the weight pocket from the Buoyancy Compensator Device (BCD) can detach during use. If this happens, the user will not... - Magnetic Drinkware Charms Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Magnets; Sold on Amazon by Maitys
Consumer productReported April 10, 2026 · The recalled magnetic drinkware charms violate the mandatory standard for magnets because they contain loose magnets posing an ingestion hazard to children.... - Silks Recall Children's Loungewear Sets Due to Risk of Serious Injury or Death from Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
Consumer productReported April 10, 2026 · The recalled children's loungewear violates mandatory flammability standards for children's sleepwear, posing a risk of serious injuries or deadly burn hazards... - SNOOZ Recalls Electrical Fans Due to Fire Hazard
Consumer productReported April 10, 2026 · The power connector inside the fan can corrode and cause the fan to overheat, posing a risk of fire. - Easymake Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Imported by ZFZG-US
Consumer productReported April 10, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed... - Vitaquest International Recalls Multiple Iron Supplement Bottles and Packets Due to Risk of Serious Injury or Death from Poisoning to Young Children; Violates Mandatory Standard for Child-Resistant Packaging
Consumer productReported April 10, 2026 · The dietary supplements contain iron, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The packaging of the... - BISSELL Recalls Over One Million Steam Shot OmniReach Steam Cleaners Due to Risk of Serious Burn Hazard from Attachments
Consumer productReported April 10, 2026 · The recalled steam cleaners' attachments can unexpectedly detach from the steam cleaners and expel hot water or steam onto users during use, posing a serious... - Wybotics Recalls Robotic Pool Vacuums Due to Burn and Fire Hazards
Consumer productReported April 10, 2026 · The lithium-ion battery in the recalled pool vacuums can overheat, posing burn and fire hazards to consumers. - MEI HEONG YUEN GARLIC FLAVOR ROASTED PEANUTS recall (Super World Trading Inc.)
FoodClass IIIReported April 8, 2026 · Products contain cyclamates (banned sweetener) - MEI HEONG YUEN WALNUT FLAVOR ROASTED PEANUTS recall (Super World Trading Inc.)
FoodClass IIIReported April 8, 2026 · Products contain cyclamates (banned sweetener) - MEI HEONG YUEN TANGERINE FLAVOR ROASTED PEANUTS recall (Super World Trading Inc.)
FoodClass IIIReported April 8, 2026 · Products contain cyclamates (banned sweetener) - Divided Sunset Multi Collagen Peptides recall (TG FOODS INC)
FoodClass IIReported April 8, 2026 · The product states wild caught marine collagen and eggshell membrane collagen in ingredient statement but does not state EGG and the specific species of FISH... - 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... - 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... - 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. - 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. - 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... - 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. - Magnesium Sulfate in Water for Injection recall (Amneal Pharmaceuticals, LLC)
DrugClass IReported April 8, 2026 · Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead. - Prazosin Hydrochloride Capsules recall (Appco Pharma LLC)
DrugClass IIReported April 8, 2026 · cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits. - Prazosin Hydrochloride Capsules recall (Appco Pharma LLC)
DrugClass IIReported April 8, 2026 · cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits. - Prazosin Hydrochloride Capsules recall (Appco Pharma LLC)
DrugClass IIReported April 8, 2026 · cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits. - Artificial Tears Sterile Lubricant Eye Drops recall (K.C. Pharmaceuticals, Inc)
DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility - STERILE EYE DROPS SOOTHING TEARS recall (K.C. Pharmaceuticals, Inc)
DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility - Sterile EYE DROPS REDNESS LUBRICANT recall (K.C. Pharmaceuticals, Inc)
DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility - Sterile Eye Drops ORIGINAL FORMULA recall (K.C. Pharmaceuticals, Inc)
DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility - Ultra Lubricating Eye Drops recall (K.C. Pharmaceuticals, Inc)
DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility - Dry Eye Relief Eye Drops recall (K.C. Pharmaceuticals, Inc)
DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility - EYE DROPS Advanced Relief recall (K.C. Pharmaceuticals, Inc)
DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility - Sterile EYE DROPS AC recall (K.C. Pharmaceuticals, Inc)
DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility - traMADol Hydrochloride Tablets recall (Amneal Pharmaceuticals, LLC)
DrugClass IIReported April 8, 2026 · Failed Impurities/Degradation Specifications: N-nitroso-desmethyl-tramadol impurity (NDSRI) was found out of the specification at 24-month stability interval... - 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... - 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.