Archive
554 recalls were announced in February 2026.
Of the 554 recalls this month scored against our rubric, 9% are Critical, 11% are Severe.
Which agencies issued them
TheKiddoSpace is recalling its Children's Montessori Egg Puzzle Toys due to a choking hazard. The recalled toys are intended for children under three years of age and the eggs can block a child's airway, posing a risk of choking and death to children.
Royal Oak Enterprises is recalling approximately 190,560 Flame Saber Lighters because they lack required child-resistant mechanisms, posing a risk of serious injury or death.
Trankerloop is recalling approximately 2,380 baby bath seats because they are unstable and can tip over, posing a risk of serious injury or death from drowning.
Grtard is recalling approximately 130 Grtard Magnet Stick Figure Men Toy Sets because they contain loose magnets that pose a serious injury or death risk if swallowed.
International is recalling certain 2023-2027 IC Bus CESB school buses because the brake lines may have been installed with incorrect hardware, which can damage the lines and cause a leak.
TheKiddoSpace is recalling approximately 9,400 fingerpainting kits because they contain hazardous substances and regulated phthalates that pose health risks to children.
Dupray USA is recalling Dupray Neat Steam Cleaners because the boiler can rupture, posing a risk of burns or serious injury. Consumers should stop using the device immediately and contact the manufacturer for a free replacement safety cap.
General Motors is recalling 2012-2013 Buick Regal vehicles in 23 states due to improper corrosion protection on rear suspension toe links, which may fracture and cause loss of control.
Surreal Brands is recalling Tubby Tots Fizzy Flask Bath Magic bath foam sets because moisture can build up pressure in the container, causing pieces to eject forcefully.
Somgem and Yomin brand lighters are being recalled because they lack required child-resistant mechanisms, posing a risk of serious injury or death from fire and burns.
BMW is recalling one 2026 S 1000 RR motorcycle because the turn signal reset button can be unintentionally activated, causing the turn signal to fail.
Todson is recalling about 40,245 Concord 360 Degree Rechargeable Light-Up Bike Helmets because they fail to meet safety standards, posing a risk of serious head injury or death.
TheKiddoSpace is recalling approximately 4,000 children's flashcard talking toys due to lead and phthalate levels that exceed federal limits and a failure to meet battery safety standards.
Sanven Technology is recalling approximately 10,400 Vevor Retractable Baby Gates because they violate safety standards and pose an entrapment risk to children.
SumDirect LED Mini Lights are recalled because the button cell batteries can be easily accessed by children, posing an ingestion hazard. No injuries have been reported.
Zelbuck Magnetism Ball Game Toys are being recalled because they contain loose magnets that pose a serious injury or death risk if swallowed.
Joyreal Busy Board children's toys are recalled due to choking and laceration hazards from a detachable small mirror with sharp edges. No injuries have been reported.
Magnetic chess games sold on Amazon by Kaiwenshangpin are recalled because loose magnets inside can be swallowed by children, potentially causing intestinal damage or death. No injuries have been reported.
TheKiddoSpace is recalling its Children's Sensory Swing because the flexible fabric can form loops that pose a risk of serious injury or death from strangulation.
Evajoy 48-inch and taller above-ground pools are recalled due to a drowning hazard. The compression strap around pool legs can create a foothold allowing child access.
About 81,800 Babysense Max View baby monitors are recalled because the display unit can overheat and spark while charging, creating a fire hazard. Hisense has received 11 incident reports with no injuries reported.
TheKiddoSpace is recalling about 19,700 children's handwriting practice kits because the pens contain lead levels that violate the federal lead content ban. No injuries have been reported.
TheKiddoSpace is recalling about 140 children's story books because felt parts can detach and pose a choking hazard. No injuries have been reported.
Andersen Windows is recalling about 91,000 window opening control devices sold as kits or installed on 100 Series casement windows because they can break or detach after impact, posing fall and serious injury hazards. No injuries have been reported.
PQL recalls about 186,520 high bay linear LED light fixtures because degrading retaining pins can cause the LED board to come loose and spark a fire. One fire has been reported with no injuries.
TheKiddoSpace is recalling its Peg Dolls in Cups Toys because the small peg dolls pose a choking hazard to children under three years old.
TheKiddoSpace is recalling approximately 300 Children's Christmas Tree Toy Play Sets because the zipper pulls contain lead levels that exceed federal limits.
Honda is recalling certain 2024 Acura ZDX and Prologue vehicles because a software error may cause the instrument panel display to fail and the rearview camera to show a blank screen in reverse.
TheKiddoSpace is recalling approximately 650 LED soccer hover balls because the battery surface temperature can exceed safety limits, posing a burn risk.
TheKiddoSpace is recalling about 4,300 reusable water balloons because the cord lock on the storage bag contains a regulated phthalate that violates the federal phthalate ban. No injuries have been reported.
About 150 Bicystar high chairs (model TB-HC6900) sold on Amazon are recalled because they lack the required crotch restraint and can trap a child's head, creating fall and entrapment hazards. No injuries have been reported.
General Motors has recalled multiple Chevrolet, GMC, Cadillac, and Buick vehicles from 2025–2027 because their radios were not properly configured to download the electronic owner's manual during production. Without the manual, owners may not know how to safely operate the vehicle.
Lotus Mom Corporation is recalling 9 units of a 4-quart Brass Pital Pot over potential contamination with leachable lead.
Art Monkey LLC is recalling 8,500 bottles of Why Not Natural Moringa Capsules because they have the potential to be contaminated with Salmonella.
Olympus Corporation of the Americas is recalling 744 Olympus High Flow Insufflation Units (Model UHI-2) because a software algorithm issue may cause overpressure events.
Reser's Fine Foods is recalling 298 tubs of tuna salad that were mislabeled with a Molly Kitchen's Chicken Salad lid, leaving fish undeclared.
Medline is recalling 27,320 labor and delivery convenience kits due to calibration issues with sterilization equipment that may affect the sterility assurance level of the devices.
Lotus Mom Corporation is recalling 56 units of the IKM Aluminum Saucepan 9" with Wooden Handle due to potential leachable lead contamination. The product was distributed in California and Colorado.
Olympus is recalling 1,538 Thunderbeat 5 mm surgical devices worldwide due to continued reports of adverse events. The recall affects all units of Model No. TB-0510IC.
Olympus is recalling 9,542 Thunderbeat surgical devices worldwide due to continued reports of adverse events. The recall affects all lots of the TB-0545FCS model.
Medline is recalling 753 units of its tracheostomy convenience kits and trach tote due to potential sterilization equipment calibration issues that may affect the sterility assurance level of the devices.
H & N Group Inc. is recalling frozen cooked medium shrimp due to potential contamination with Cesium-137 from manufacturing under insanitary conditions. The product was distributed to approximately 30 retail locations in the greater Houston and Gulf Coast areas.
Medline is recalling 448 units of its BASIC NERVE BLOCK TRAY W/LINEN (Model PAIN0150C) due to calibration issues with sterilization and packaging equipment that could affect the sterility assurance level of the devices.
Medline is recalling 291 units of three burn care convenience kits due to calibration issues with sterilization and packaging equipment that may affect sterility assurance.
Olympus is recalling 485 High Flow Insufflation Units (Model UHI-3) nationwide due to a software algorithm issue that may cause dangerous overpressure during abdominal surgery.
Wilson-Cook Medical Inc. is recalling 153 Teslatome Bipolar Sphincterotomes due to a potential void in the material separating the wire guide and cutting wire lumens, which may cause an inappropriate path of current during cutting.
Olympus Corporation of the Americas is recalling the Olympus High Flow Insufflation Unit (Model UHI) because a software algorithm issue may cause overpressure events.
Integra LifeSciences is recalling 2,906 units of its Private Label CVS wound dressings (Model CVS405406) due to potential packaging failures that could compromise the sterile barrier.
Medline is recalling 12,418 units of various surgical convenience kits due to calibration issues with equipment used for sterilization and packaging, which may affect the sterility assurance level of the devices.
Medline is recalling 4,757 units of convenience surgical kits distributed worldwide due to calibration issues with sterilization and packaging equipment that may affect sterility assurance.
Olympus is removing the Olympus Thunderbeat, 5 mm, 45 cm, Pistol Grip from the market, stating the action is due to continued reports of adverse events.
Medica Corporation is recalling 1,578 capillary tube kits after a systematic positive bias of up to 20% was identified across the reportable potassium range.
Olympus is removing the Olympus Thunderbeat 5 mm, 35 cm, Front-Actuated Grip from the market, stating the action is due to continued reports of adverse events.
Medline Industries is recalling cardiac surgical convenience kits due to sterilization equipment calibration issues that could affect device sterility assurance levels.
Olympus is removing the Olympus Thunderbeat, 5 mm, 20 cm, Inline Grip from the market, stating the action is due to continued reports of adverse events.
Medline is recalling 23,238 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Olympus Corporation of the Americas is removing Olympus Thunderbeat 5 mm, 45 cm Front-Actuated Grip devices due to reports of adverse events.
Centinel Spine is recalling 20 Prodisc C SK total cervical disc replacements because products were mislabeled as the 6mm product but included the 5mm product.
Intuitive Surgical, Inc. is recalling the Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 due to a software error that can cause loss of user interface content on monitors.
Olympus Corporation of the Americas is removing Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip devices due to reports of adverse events.
Medline is recalling 32 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline is recalling 72 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Olympus Corporation is recalling 30 Thunderbeat 5 mm, 45 cm Inline Grips due to continued reports of adverse events during medical procedures.
Medline is recalling 117,907 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline is recalling 4,525 C-section convenience kits worldwide due to calibration issues with sterilization and packaging equipment that could affect sterility assurance.
Medline is recalling 30,958 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline Industries is recalling 4,853 medical device kits due to potential sterility issues from equipment calibration problems during manufacturing.
Medline is recalling 3,561 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline Industries, LP is recalling specific Medline Convenience Kits (CHEST/BREAST-LF) because equipment calibration issues may have impacted the sterility assurance level of the products.
Medline Industries, LP is recalling various Medline Convenience Kits because equipment calibration issues may have impacted the sterility assurance level of the products.
Medline Industries, LP is recalling certain Medline Convenience Kits because equipment calibration issues may have impacted the sterility assurance level of the products.
Medline is recalling 59 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Integra LifeSciences is recalling 49,367 units of MediHoney Gel with Active Leptospermum Honey over potential packaging failures that could breach the sterile barrier.
Medline is recalling 82,597 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Stryker is recalling the MOLLI 2 System due to magnetized surgical tools that may dislodge markers during target tissue removal procedures. The recall affects 5,864 units distributed worldwide.
Medline is recalling 240 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline is recalling 108 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Auris Health is recalling 173 MONARCH Platform bronchoscopy systems because a software restart can re-initialize the system to patient-left, leading to unanticipated robotic arm positioning.
Olympus Corporation of the Americas is removing Olympus Thunderbeat 5mm, 35 cm, Pistol Grip devices due to reports of adverse events.
Lotus Mom Corporation is recalling 10 units of a Brass Tope over potential contamination with leachable lead.
Medline is recalling 193,157 units of surgical packs because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline is recalling 5,346 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Olympus Corporation of the Americas is removing Olympus Thunderbeat 5 mm, 35 cm, Front-Actuated Grip Type S devices due to reports of adverse events.
Medline is recalling 7,725 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Bard Peripheral Vascular is recalling 14,935 Broviac 4.2 Fr single-lumen CV catheter cutdown trays because damage to the outer tray can potentially compromise the sterile barrier.
Medline Industries, LP is recalling various Medline Convenience Kits because equipment calibration issues may have impacted the sterility assurance level of the products.
Medline is recalling 684 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline is recalling 175 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline Industries, LP is recalling various Medline Convenience Kits because equipment calibration issues may have impacted the sterility assurance level of the products.
Medline is recalling 15 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Woodland Foods is recalling 30,030 lbs of Woodland Gourmet Arrowroot Flour over the possible presence of foreign material.
Medline is recalling 14,927,765 units of surgical drapes because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline is recalling 1,070 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline Industries is recalling 779 units of convenience kits and setup trays due to potential sterility assurance issues from equipment calibration problems during manufacturing.
Medline is recalling 9,720 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline is recalling 70,376,042 units of surgical gowns because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline is recalling 7,575 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline is recalling 808 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Medline is recalling 553 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Baxter Healthcare is recalling 5 Spectrum IQ Infusion Pumps because they were released without full testing being performed, including occlusion alarm testing.
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