Recalls in Vermont (page 30)
3845 recalls.
- 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. - Samson International Recalls Bellevue and Oaklynn Canopy Bed Frames Due to Impact and Injury Hazards
Consumer productReported April 3, 2026 · The canopy beams of the bed frames can collapse primarily when the bed is moved, posing impact and injury hazards to consumers. - Tuymec Minoxidil Hair Growth Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by DrHealBeauty
Consumer productReported April 3, 2026 · The hair serum contains minoxidil, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The hair serum's packaging is... - Sam's Club Recalls Member's Mark Children's Pajama Sets Due to Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
Consumer productReported April 3, 2026 · The recalled pajama sets violate the mandatory standards for flammability of children's sleepwear, posing a risk of burn injuries to children. - HTRC and Haisito T400 Battery Chargers Recalled Due to Risk of Serious Injury and Death from Fire Hazard; Manufactured by Huizhou Haitan Technology
Consumer productReported April 3, 2026 · The chargers can ignite or cause a connected battery to ignite, posing a fire hazard and risk of serious injury and death. - Sangohe Reannounces and Expands Adult Portable Bed Rails Recall Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails
Consumer productReported April 3, 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... - E Mishan Recalls Granitestone Diamond Pro Blue Stainless Sauté Pans Due to Impact and Burn Hazards
Consumer productReported April 3, 2026 · The metal cap on the screw that connects the sauté pan to the handle can become detached and forcefully eject when heated, posing impact and burn hazards to... - TecFlox Hair and Beard Growth Serum Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
Consumer productReported April 3, 2026 · The hair and beard growth serum contains minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The bottles... - ELENKER Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Fuzhou Shiahaha Cultural Industry Development
Consumer productReported April 3, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped... - OCUN NA Recalls Condor HMS Triple Carabiners Due to Risk of Serious Injury or Death from Fall Hazard
Consumer productReported April 3, 2026 · The carabiner's gate can malfunction where the gate does not close automatically and has to be closed manually by hand, posing a risk of serious injury or... - Coluans Christmas Light-Up Rings Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Toys; Sold on Amazon by BUDI Official
Consumer productReported April 3, 2026 · The recalled light-up rings violate the mandatory safety standard for toys because the battery compartment within the LED light ring contains button cell... - Gavoyeat Halloween Light-Up Rings Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Toys; Sold on Amazon by CSZWEICD
Consumer productReported April 3, 2026 · The recalled light-up rings violate the mandatory safety standard for toys because the battery compartment within the LED light ring contains button cell... - Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violates the Small Ball Ban; Sold on Amazon by Beestech
Consumer productReported April 3, 2026 · The recalled spiral tower toy sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years of... - 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... - 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... - Nuts.com recall (Nuts.com Inc.)
FoodClass IReported April 1, 2026 · Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient statement and allergen information do not include wheat or soy. - Chilli Spanish Peanuts recall (Western Mixers Produce & Nuts, Inc.)
FoodClass IIReported April 1, 2026 · Foreign object (glass) found inside sealed container of finished product. - Chilli Spanish Peanuts recall (Western Mixers Produce & Nuts, Inc.)
FoodClass IIReported April 1, 2026 · Foreign object (glass) found inside sealed container of finished product. - Meclizine Hydrochloride Tablets recall (Amerisource Health Services LLC)
DrugClass IIReported April 1, 2026 · Failed tablet specifications. - Octreotide Acetate for Injectable Suspension recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported April 1, 2026 · Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract... - Octreotide Acetate for Injectable Suspension recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported April 1, 2026 · Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract... - Octreotide Acetate for Injectable Suspension recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported April 1, 2026 · Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract... - Levothyroxine Sodium Tablets USP 150 mcg recall (MACLEODS PHARMA USA, INC)
DrugClass IIReported April 1, 2026 · Subpotent Drug - CUROSURF recall (Chiesi USA, Inc.)
DrugClass IIReported April 1, 2026 · Lack of Assurance of Sterility - Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit recall (Radnostix)
DrugClass IIIReported April 1, 2026 · Failed Tablet/Capsule Specifications - 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... - 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... - 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 - MPINOI Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Bioenrrty
Consumer productReported March 27, 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... - DIY Cold Plunge Recalls Sauna Heater Kits Due to Risk of Serious Injury or Death from Fire Hazard
Consumer productReported March 27, 2026 · Electrical conductors within the sauna heater kits can overheat, posing a fire hazard and risk of serious injury or death. - FUNTOK Ride-On Trucks Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Imported by Shenzhen Luobei Trading
Consumer productReported March 27, 2026 · The truck's circuit board can overheat and ignite, posing fire and burn hazards. - Petzl America Recalls Nomic and Ergonomic Ice Climbing Axes Due to Fall Hazard; Risk of Serious Injury or Death
Consumer productReported March 27, 2026 · The ice axe shaft can break at the handle during use, posing a fall hazard, which can result in serious injury or death. - CCCEI Brand Power Strips Recalled Due to Risk of Serious Injury or Death from Fire; Sold by Middle Way Electronics
Consumer productReported March 27, 2026 · The power strips do not contain supplementary overcurrent protection, which creates a risk of fire if the power strips are overloaded. The resulting fire can... - GLMZZ Fidget Magnet Ball Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
Consumer productReported March 27, 2026 · The magnet ball toys violate the mandatory standard for toys because they are high-powered magnets, posing an ingestion hazard to children. When high-powered... - Sunnyyes LED Mini Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries
Consumer productReported March 27, 2026 · The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because the lights contain lithium coin... - DuraTrac Recalls Stainless Steel Gas Connectors Due to Fire Hazard
Consumer productReported March 27, 2026 · The recalled DuraTrac gas connectors contain a manufacturing defect that could cause a gas leak, posing a fire hazard to consumers. - AirClub Convertible Bassinets Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Bedside Sleepers
Consumer productReported March 27, 2026 · The recalled convertible bassinets violate the mandatory standard for bedside sleepers because the mechanism used to attach the product to the adult bed... - Vive Health Recalls Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Two Deaths Reported
Consumer productReported March 27, 2026 · When the recalled bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress. This... - 4our Kiddies Tip Restraint Kits Recalled Due to Tip-Over Hazard; Risk of Serious Injury and Death
Consumer productReported March 27, 2026 · The recalled plastic tip restraint kits (also referred to as furniture straps) can break or degrade, posing tip-over and entrapment hazards that can result in... - Nexgrill Recalls Over 10.2 Million Metal Wire Bristle Grill Brushes Due to Ingestion Hazard; Sold at Home Depot
Consumer productReported March 27, 2026 · Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that... - Webcol Alcohol Prep pad recall (Cardinal Health 200, LLC)
DrugClass IReported March 25, 2026 · Non-Sterility: microbial contamination identified as Paenibacillus phoenicis - Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%* recall (Apotex Corp.)
DrugClass IIReported March 25, 2026 · Lack of Assurance of Sterility - Dexamethasone Sodium Phosphate Injection recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIReported March 25, 2026 · Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were above specs... - Children's Ibuprofen Oral Suspension recall (STRIDES PHARMA INC)
DrugClass IIReported March 25, 2026 · Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product. - 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. - Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number:... recall (Diagnostica Stago, Inc.)
Medical deviceClass IIReported March 25, 2026 · After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range. - Convatec recall (ConvaTec, Inc)
Medical deviceClass IIReported March 25, 2026 · Drainable large pouch may leak due to manufacturing issue. - Convatec recall (ConvaTec, Inc)
Medical deviceClass IIReported March 25, 2026 · Drainable large pouch may leak due to manufacturing issue. - Convatec recall (ConvaTec, Inc)
Medical deviceClass IIReported March 25, 2026 · Drainable large pouch may leak due to manufacturing issue. - Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion ... recall (Elekta, Inc.)
Medical deviceClass IIReported March 25, 2026 · Due to adapter not being properly aligned or locked in place. - Cub Pediatric Crib recall (Stryker Medical Division of Stryker Corporation)
Medical deviceClass IIReported March 25, 2026 · Cribs sold in the USA are missing two access door warning labels.