Recalls in Virginia (page 39)
4022 recalls.
- Medline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) ROBOTIC recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) WCH BARI-GASTRECTOMY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is... recall (Diagnostica Stago, Inc.)
Medical deviceClass IIReported January 21, 2026 · Potential for defect for Asserachrom HPIA lot 271288, which can affect every well in the impacted strip and produce negative results. - Philips Azurion Systems R3.0. Includes the following label descriptions and... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Nine (9) identified software issues which may result in the following: loss of X-ray after Pedal Tap, loss of X-ray after Phase Fault, missing live X-ray on... - MOSAIQ Oncology Information System with Particle Therapy License recall (Elekta, Inc.)
Medical deviceClass IIReported January 21, 2026 · Using oncology information system that manages workflow may result in overtreatment if:Plan delivered with Particle Therapy IHE-RO TDW-II interface,With one... - Allura Xper FD20/20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 Biplane recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 Biplane recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10F recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Product Name: Allura Xper FD10C recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - BD Ready-to-Use Hydrophilic Catheter 14 Fr recall (HANGZHOU BEVER MEDICAL DEVICES CO., LTD.)
Medical deviceClass IIReported January 21, 2026 · Labeling error, Incorrect expiration date - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - A71200 Vanta" Clinician Programmer Application recall (Medtronic Neuromodulation)
Medical deviceClass IIReported January 21, 2026 · Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure. - Curtis International Expands Recall of Frigidaire-brand Minifridges Due to Fire and Burn Hazards
Consumer productReported January 16, 2026 · The minifridges' internal electrical components can short circuit and ignite the surrounding plastic housing, posing fire and burn hazards. - RootStim Recalls Beard Growth Serum Spray Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
Consumer productReported January 16, 2026 · The beard growth serum contains minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The serum's... - Greatale Recalls Self-Feeding Pillows Due to Risk of Serious Injury or Death from Aspiration and Suffocation
Consumer productReported January 16, 2026 · The recalled self-feeding pillows hold the bottle at an unsafe angle while keeping it fixed in place so the infant cannot pull away. This can lead to... - HEZI Brand Power Strips Recalled Due to Risk of Serious Injury or Death from Electrocution; Sold by HEZI HOME
Consumer productReported January 16, 2026 · The power strips have an ungrounded metal enclosure that poses an electrocution hazard if energized, resulting in serious injury or death. - Morgan Lane Recalls Children's Pajama Sets Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Flammability Standards for Children's Sleepwear
Consumer productReported January 16, 2026 · The recalled children's pajamas violate the mandatory standards for flammability of children's sleepwear, posing a risk of serious injury and deadly burn... - Adams Manufacturing Recalls Adirondack Patio Chairs Due to Injury and Fall Hazards
Consumer productReported January 16, 2026 · The recalled chairs can crack and collapse, posing injury and fall hazards. - Yixing Trading Recalls KEAWIS Crib Mattresses Due to Risk of Serious Injury or Death from Entrapment and Suffocation; Violates Mandatory Standard for Crib Mattresses
Consumer productReported January 16, 2026 · The aftermarket mattresses violate the mandatory standard for crib mattresses, as the mattresses may not adequately fit certain play yards or non-full-sized... - R.X.Y Bicycle Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
Consumer productReported January 16, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional... - BBWOO Baby Loungers Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
Consumer productReported January 16, 2026 · The recalled baby loungers violate the mandatory safety standard for Infant Sleep Products. The sides are too low to contain an infant and the enclosed... - Energizer Recalls Rechargeable Lanterns Due to Overheating
Consumer productReported January 16, 2026 · The lithium-ion batteries installed in the lanterns can overheat, posing a burn hazard to consumers. - Ruahouine Hair Growth Serum Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Ruahouine
Consumer productReported January 16, 2026 · The serum bottles contain minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The serum's packaging is... - Bengal King Jhal Chanachur food treats 12.34oz recall (South Asian Food Inc.)
FoodClass IReported January 14, 2026 · Contains undeclared peanuts - Locatelli Grated Pecorino Romano 48/8oz Shipper recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Ambriola Piccante grated Pecorino Romano recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Boar's Head Pecorino Romano Grated recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Sam's Pecorino Romano grated recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Boar's Head Grated Pecorino Romano recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Pinna Grated Pecorino Romano 2/10 recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Locatelli Grated Pecorino Romano recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Locatelli Grated Pecorino Romano 4 oz and 8 oz plastic cup & lid recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Codman CereLink... recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported January 14, 2026 · Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits. - Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN... recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported January 14, 2026 · Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits. - BD Pyxis ES Enterprise Server Catalog Numbers 1115-00 recall (CareFusion 303, Inc.)
Medical deviceClass IIReported January 14, 2026 · Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems. - Philips Tempus Pro Patient Monitor recall (Remote Diagnostic Technologies Ltd.)
Medical deviceClass IIReported January 14, 2026 · Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure (BDR) but ICP and BDR measurements have not been tested or validated for accuracy. If... - Baraka Gourmet Pastry Kunafe 6.7oz. recall (ZIYAD BROTHERS IMPORTING)
FoodClass IIReported January 14, 2026 · May contain partially hydrogenated oils - Baraka French Style Puff Pastry 1lb and 1.5lbs sizes recall (ZIYAD BROTHERS IMPORTING)
FoodClass IIReported January 14, 2026 · May contain partially hydrogenated oils - Rosuvastatin Tablets recall (AvKARE)
DrugClass IIReported January 14, 2026 · Out of specification for dissolution. - ClearLife Allergy Nasal Spray recall (Medinatura New Mexico, inc.)
DrugClass IReported January 14, 2026 · Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter. - ReBoost Nasal Spray recall (Medinatura New Mexico, inc.)
DrugClass IReported January 14, 2026 · Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter. - Oxycodone and Acetaminophen CII Tablets USP recall (SpecGx, LLC)
DrugClass IIReported January 14, 2026 · Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets. - Oxycodone and Acetaminophen CII Tablets USP recall (SpecGx, LLC)
DrugClass IIReported January 14, 2026 · Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets. - Tri-Moxi+¿ recall (Imprimis NJOF, LLC)
DrugClass IIReported January 14, 2026 · Presence of particulate matter - Glass like particles. - Dexamethasone Moxifloxacin Ketorolac recall (Imprimis NJOF, LLC)
DrugClass IIReported January 14, 2026 · Presence of particulate matter - Glass like particles. - Dexamethasone Moxifloxacin recall (Imprimis NJOF, LLC)
DrugClass IIReported January 14, 2026 · Presence of particulate matter - Glass like particles. - Fesoterodine Fumarate recall (Alembic Pharmaceuticals Limited)
DrugClass IIIReported January 14, 2026 · Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit. - Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK recall (Medline Industries, LP)
Medical deviceClass IIReported January 14, 2026 · Firm received multiple complaints regarding tubing disconnecting from oxygen mask. If issue occurs during use, may lead to delay in patient care and patient... - Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog Number:... recall (IMRIS Imaging Inc)
Medical deviceClass IIReported January 14, 2026 · Torque screw may crack or separate. If used, an affected screw could lead to inadequate head stabilization, compromised surgical precision, procedural delays... - Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor. recall (Philips North America Llc)
Medical deviceClass IIReported January 14, 2026 · It was found that the MX40 device could not reconnect to the PIC iX when moving between Radiohead and Trident 1.4 GHz access points if the signal strength... - Arial 900 MHz Call Station recall (Securitas Healthcare LLC)
Medical deviceClass IIReported January 14, 2026 · Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1)... - Arial 900 MHz Call Station recall (Securitas Healthcare LLC)
Medical deviceClass IIReported January 14, 2026 · Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1)... - The Pressio 2 ICP Monitoring System recall (Sophysa)
Medical deviceClass IIReported January 14, 2026 · Customer complaints of Pressio monitor rebooting. - Beckman Coulter UniCel Dxl 800 recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported January 14, 2026 · Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard... - Beckman Coulter UniCel Dxl 600 recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported January 14, 2026 · Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard... - Revogene C. difficile recall (Meridian Bioscience Inc)
Medical deviceClass IIReported January 14, 2026 · The affected lots show a decline in performance over time, which may lead to false-negative results. - The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay with... recall (Roche Diagnostics Operations, Inc.)
Medical deviceClass IIReported January 14, 2026 · Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator Lot-to-Lot Variability. Issues may lead to delayed or incorrect diagnosis, as well as... - Joyful Journeys Recalls Baby Loungers Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products
Consumer productReported January 9, 2026 · The recalled baby loungers violate the mandatory safety standard for Infant Sleep Products. The sides are too low to contain an infant and the enclosed... - PNW Components Recalls Aluminum Alloy Bicycle Pedals Due to Crash Hazard
Consumer productReported January 9, 2026 · The pedal axle can crack, causing the pedal to detach from the crank, posing a fall hazard to the rider. - Isla Rae Magnetic Wireless Chargers Recalled Due to Fire and Burn Hazards; Sold by TJX at T.J. Maxx and Marshalls Stores
Consumer productReported January 9, 2026 · The chargers can explode while in use, posing a fire and burn hazard. - Kori Gey Water Toy Kits Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Qaniy
Consumer productReported January 9, 2026 · The recalled toy kits violate the mandatory standard for toys containing button cell batteries because the compartment that holds the batteries can be easily... - RH Recalls Natural Antler Chandeliers Due to Impact Hazard
Consumer productReported January 9, 2026 · If the chandelier is hung at an angle on a vaulted ceiling or a sloped beam, the chandelier's canopy hardware can break, causing the chandelier to detach and... - Pounding Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion Hazard; Violate Mandatory Standard for Toys; Sold on Amazon by Findriver and Weeksome
Consumer productReported January 9, 2026 · The recalled pounding toys violate the mandatory standard for toys because they contain high-powered magnets, which can detach, posing an ingestion hazard to... - YOLAAH Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violate Mandatory Standard for Adult Portable Bed Rails
Consumer productReported January 9, 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... - Vasicar 18-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates Mandatory Standard for Clothing Storage Units
Consumer productReported January 9, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Sangohe 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
Consumer productReported January 9, 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... - Rattan 6-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by Rattan
Consumer productReported January 9, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in a risk of serious injuries... - NFSVLB Baby Bath Seats Recalled Due to Risk of Serious Injury or Death to Children from Drowning and Entrapment; Violate Mandatory Standard for Infant Bath Seats; Sold on Amazon by NFSVLB
Consumer productReported January 9, 2026 · The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, and have leg openings... - Marcus Adler Glove Recalls Julie and Judah Pajama Pants and Shorts Due to Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
Consumer productReported January 9, 2026 · The pajama pants and shorts violate the mandatory standards for flammability of children's sleepwear, posing a risk of burn injuries to children. - The Kalencom Corporation Recalls SARO Braided Crib Bumpers Due to Risk of Serious Injury or Death from Suffocation; Violates Federal Crib Bumper Ban
Consumer productReported January 9, 2026 · The recalled padded crib bumpers violate the federal ban on crib bumpers because they can obstruct an infant's breathing, posing a risk of serious injury or... - Infant Innovations Recalls BabyBond Retractable Safety Gates Due to Risk of Serious Injury or Death to Children from Entrapment; Violates Mandatory Standard for Gates and Enclosures
Consumer productReported January 9, 2026 · The recalled gates violate the mandatory standard for expansion gates and expandable enclosures because a child's torso can fit through the opening between the... - DR Power Equipment Reannounces and Expands Recall of Leaf Vacuums Due to Laceration Hazard; New Remedy Available
Consumer productReported January 9, 2026 · Pieces from the recalled leaf vacuums can come loose inside the unit, or debris can pierce the chute, resulting in material ejecting and posing a laceration... - Agrish 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 Agrish Direct
Consumer productReported January 9, 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... - Tom Bumble Nutty Peanut Butter Flake Candy with Peanut & Chocolate GF V. Product is... recall (Tom Bumble LLC)
FoodClass IIReported January 7, 2026 · Foreign material.