Safety Recalls
RSS ↗15,184 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 1,851–1,900 of 15,184
- Class II
Food Recall · February 26, 2026
Pepsin Full Strength Powder, 50 kg, Item #5000545, American Laboratories 5036 South 33rd Street, Omaha, Nebraska 68107. Packed in double poly-lined cardboard drums or boxes.Potential Salmonella contamination.
- Unclassified
Consumer Product Recall · February 26, 2026
SN Commerce LLC, dba TheKiddoSpaceStore, of Dover, Delaware
TheKiddoSpace Children's Montessori Egg ToysThe 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.
- Class I
Food Recall · February 26, 2026
Butter Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly linerPositive Salmonella contamination
- Unclassified
Consumer Product Recall · February 26, 2026
Andersen Windows, Inc., of Bayport, Minnesota
Window opening control devices sold as kits or installed on 100 Series casement windowsThe window opening control devices can break or detach after accidental or other impact, allowing the window to be opened, posing fall and serious injury hazards.
- Unclassified
Consumer Product Recall · February 26, 2026
Dongguan Fuxin E-Commerce Co., Ltd., dba SumDirect, of China
SumDirect LED Mini LightsThe recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings as required by Reese's Law. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- Unclassified
Consumer Product Recall · February 26, 2026
Shenzhen Danya Tech Co., Ltd. d/b/a Evajoy, of China
Evajoy 48-inch and taller above-ground poolsThe compression strap that surrounds the outside of the pool legs may create a foothold, allowing a child access to the pool, posing a drowning risk.
- Unclassified
Consumer Product Recall · February 26, 2026
Sanven Technology Ltd., dba Vevor, of Rancho Cucamonga, California
Vevor Retractable Baby GatesThe recalled gates violate the mandatory standard for expansion gates and expandable enclosures because a child's torso can fit through the opening between the gate and the floor, posing a risk of serious injury due to entrapment.
- Unclassified
Consumer Product Recall · February 26, 2026
SN Commerce LLC, dba TheKiddoSpaceStore, of Dover, Delaware
TheKiddoSpace Print and Cursive Handwriting KitsThe pens in the recalled children's handwriting kits contain levels of lead in the nib that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues.
- Unclassified
Consumer Product Recall · February 26, 2026
Shenzhen Elephant Outdoor Information Technology Inc. dba Elepdv, of China
Somgem Lightweight Tiny Pinky Pig and Yomin Toilet LightersThe recalled pig and toilet lighters violate the mandatory standard for cigarette lighters because they do not have the required child-resistant mechanisms, posing a serious risk of injury or death from fire and burn hazards. The recalled pig and toilet lighters violate the mandatory standard for cigarette lighters because they do not have the required child-resistant mechanisms, posing a serious risk of injury or death from fire and burn hazards.
- Unclassified
Consumer Product Recall · February 26, 2026
Royal Oak Enterprises, LLC, dba Royal Oak of Roswell, Georgia
Royal Oak Flame Saber LightersThe recalled lighters violate the mandatory standard for multipurpose lighters because they do not have the required child-resistant mechanisms, posing a risk of serious injury or death from fire and burn hazards. The lighters also violate the labeling requirements under the Federal Hazardous Substances Act by missing required safety information.
- Class II
Drug Recall · February 26, 2026
Semaglutide Inj., 2 mg x 5, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-001-06Lack of Assurance of Sterility
- Class II
Drug Recall · February 26, 2026
Tirzepatide Inj, 10mg, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-002-03.Lack of Assurance of Sterility
- Class II
Drug Recall · February 26, 2026
Semaglutide Inj, 2mg x 10, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-001-07.Lack of Assurance of Sterility
- Class II
Drug Recall · February 26, 2026
Tirzepatide Inj, 15mg x 4, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-002-04.Lack of Assurance of Sterility
- Class I
Food Recall · February 26, 2026
Butter-Rich Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly linerPotential Salmonella contamination
- Unclassified
Consumer Product Recall · February 26, 2026
SN Commerce LLC, dba TheKiddoSpaceStore, of Dover, Delaware
KiddoSpace Children's Flashcard Talking ToysThe recalled children's flashcard toy sets contain levels of lead that exceed the federal lead content ban and levels of phthalates that exceed the federal phthalates ban. Lead and phthalates are toxic if ingested by young children and can cause adverse health issues. In addition, the flashcards also violate the mandatory standard for toys because they fail to comply with the short circuit protection requirement for battery-operated toys.
- Unclassified
Consumer Product Recall · February 26, 2026
Trankerloop Baby Bath SeatsThe recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.
- Unclassified
Consumer Product Recall · February 26, 2026
Guangzhou Mengli Trading Co., Ltd., dba Indream Store, of China
Joyreal Busy Board ToysThe recalled children's toys violate the small parts ban because the small mirror can detach from the toy, posing a deadly choking hazard. In addition, the toys violate the mandatory standard for toys because the toy's mirror has sharp edges, posing a laceration hazard.
- Unclassified
Consumer Product Recall · February 26, 2026
Babysense Max View Baby MonitorsThe display or "parent" unit of the Max View baby monitors can overheat and/or spark when charging, posing a fire hazard to consumers.
- Unclassified
Consumer Product Recall · February 26, 2026
Grtard Magnet Stick Figure Men Toy SetsThe magnetic stick figure toy sets violate the mandatory standard for toys because they contain loose magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
- Unclassified
Consumer Product Recall · February 26, 2026
Hebei Beihong Kejiyouxiangongsi, dba Bicystar Group Co., Ltd. and Bicystar Store, of China
High ChairsThe high chairs violate the mandatory standard for high chairs because they were sold without the required attached crotch restraint, posing a deadly fall hazard for children. In addition, a child's head can become trapped between the seat and the side of the high chair, posing a deadly entrapment hazard.
- Unclassified
Consumer Product Recall · February 26, 2026
SN Commerce LLC, dba TheKiddoSpaceStore, of Dover, Delaware
Children's Christmas Tree Toy Play SetsThe zipper pull on the music box compartment of the recalled Christmas Tree Toys contain levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues. Additionally, the Christmas tree component fails to comply with various mechanical and electrical requirements for battery-operated toys.
- Class I
Food Recall · February 26, 2026
House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tubUndeclared egg
- Class II
Food Recall · February 26, 2026
Pepsin 1:3000 Powder, 50 kg, Item #FTI-G0193-00, American Laboratories 5036 South 33rd Street, Omaha, Nebraska 68107. Packed in double poly-lined cardboard drums or boxes.Potential Salmonella contamination.
- Class II
Food Recall · February 26, 2026
Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00, American Laboratories 5036 South 33rd Street, Omaha, Nebraska 68107. Packed in double poly-lined cardboard drums or boxes.Potential Salmonella contamination.
- Unclassified
Consumer Product Recall · February 26, 2026
Dupray USA LLC, of Newark, Delaware
Dupray Neat Steam CleanersThe steam cleaner's boiler can rupture if it is overfilled, corroded and the pressure release valve malfunctions, posing risk of burn hazards or serious injury to users or bystanders.
- Unclassified
Consumer Product Recall · February 26, 2026
Jiangsu Ever-Tie Lighting Co., Ltd, of China
High Bay Linear LED light fixturesThe retaining pins used to secure the LED board inside some units can degrade, the LED board to come loose inside the fixture, posing a fire hazard.
- Unclassified
Consumer Product Recall · February 26, 2026
Yiwushixiuxiangfushiyouxiangongsi ("Yiwu Xiu Xiang Garment Co., Ltd.") dba Kaiwenshangpin, of China
Magnetic Chess GamesThe recalled magnetic chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
- Unclassified
Consumer Product Recall · February 26, 2026
Surreal Brands LLC, of Brooklyn, New York
Tubby Tots Fizzy Flask Bath Magic bath foam setMoisture trapped inside the bath foam set container can cause pressure to build up, allowing pieces to be forcefully ejected when opened, posing an impact hazard.
- Unclassified
Consumer Product Recall · February 26, 2026
SN Commerce LLC, dba TheKiddoSpaceStore, of Dover, Delaware
TheKiddoSpace Fingerpainting KitsThe recalled children’s fingerpainting kits contain the hazardous substances methanol and ethylene glycol and are intended for children under 12 years of age, which violate the Federal Hazardous Substances Act. The products also contain a regulated phthalate, which violate the federal phthalate ban; phthalates are toxic if ingested by young children and can cause adverse health effects.
- Unclassified
Consumer Product Recall · February 26, 2026
SN Commerce LLC, dba TheKiddoSpaceStore, of Dover, Delaware
TheKiddoSpace Children's Sensory SwingThe recalled swing's flexible fabric can form loops that can entangle a child's head or neck, posing a risk of serious injury or death from strangulations.
- Unclassified
Consumer Product Recall · February 26, 2026
SN Commerce LLC, dba TheKiddoSpaceStore, of Dover, Delaware
TheKiddoSpace Children's Story BooksThe recalled book's felt parts can detach, posing a choking hazard.
- Unclassified
Consumer Product Recall · February 26, 2026
SN Commerce LLC, dba TheKiddoSpaceStore, of Dover, Delaware
TheKiddoSpace LED Soccer Hover BallsThe surface temperature of the recalled toys' batteries exceeds the allowable limit, which violates the standard for toys, posing a risk of burn injuries.
- Unclassified
Consumer Product Recall · February 26, 2026
SN Commerce LLC, dba TheKiddoSpaceStore, of Dover, Delaware
TheKiddoSpace Peg Dolls in Cups ToysThe recalled toys are intended for children under three years old and the toy's peg dolls can block a child's airway, which violate the small parts ban, posing a risk of choking and death to children.
- Unclassified
Consumer Product Recall · February 26, 2026
SN Commerce LLC, dba TheKiddoSpaceStore, of Dover, Delaware
TheKiddoSpace Reusable Water BalloonsThe cord lock on the recalled water ballons' storage bags contain a regulated phthalate, which violate the federal phthalate ban. Phthalates are toxic if ingested by young children and can cause adverse health effects.
- Unclassified
Consumer Product Recall · February 26, 2026
Todson, Inc., of Foxboro, Massachusetts
Concord 360 Degree Rechargeable Light-Up Bike HelmetThe recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the retention system and positional stability requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.
- Unclassified
Consumer Product Recall · February 26, 2026
Zelbuck Magnetism Ball Game ToysThe recalled children's chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, they can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
- Class III
Food Recall · February 25, 2026
WeiKFiELD Custard Powder Kesar Pista, Net Wt. 300g (10.6 OZ.), Poly Jar , 24 units per outer case.The ingredient, Pista, currently declared on our label should be corrected to the standard American nomenclature, Pistachio.
- Class II
Medical Device Recall · February 25, 2026
Medline Kits: 1) CATH LAB CDS, Model Number: CDS840228F; 2) IR PACK, Model Number: DYNDH2104; 3) CARDIAC CATH PACK-LF, Model Number: DYNJT2164M; 4) ANGIOGRAPHY TRAY, Model Number: DYNJT3078; 5) CAThe 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
- Class II
Medical Device Recall · February 25, 2026
Medline Kits: 1) GYN LAPAROSCOPY PACK, Model Number: DYNJ41257FThe 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
- Class II
Medical Device Recall · February 25, 2026
Medline Kits: 1) ARTHROSCOPY PACK, Model Number: DYNJ82440The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
- Class II
Medical Device Recall · February 25, 2026
2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US.A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread.
- Class III
Food Recall · February 25, 2026
Tipp Distributors, Inc. dba Novamex
C2O Coconut Water with Pulp (17.5 oz) 15 Pack UPC: 8-50274-00792-8The outer cardboard box for the canned coconut water has the incorrect Nutrition Facts Panel and Ingredient List, which does not include added sugar (5g per 17.5oz can), while the primary packaging (the can) has the correct Nutrition Facts Panel and Ingredient List.
- Class II
Medical Device Recall · February 25, 2026
Medline Kits: 1) NEWBORN ADMISSION, Model Number: DYKB1038; 2) DRAINAGE TRAY, Model Number: DYNDA3188; 3) VA ORLANDO SHOULDER PACK, Model Number: DYNJG001027B; 4) TUMESCENT SYRINGE KIT, Model NThe 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
- Class II
Medical Device Recall · February 25, 2026
Medline Kits: 1) ARTHROGRAM TRAY, Model Number: DYNJ07425; 2) TOL NEURO ANGIO PACK, Model Number: DYNJ38610I 3) ANGIOGRAPHY PACK, Model Number: DYNJ45234A 4) C.I.C.N. ANGIO PACK, Model Number: DYThe 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
- Class II
Medical Device Recall · February 25, 2026
Medline Kits: 1) BREAST PACK, Model Number: DYNJ66777DThe 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
- Class II
Medical Device Recall · February 25, 2026
Medline Kits: 1) HYSTEROSCOPY PACK, Model Number: DYNJ48399C; 2) SLING PACK, Model Number: DYNJ62849BThe 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
- Class II
Medical Device Recall · February 25, 2026
Olympus Corporation of the Americas
Brand Name: Olympus HALO PKS Cutting Forceps, 5mm 33cm Product Name: HALO PKS Cutting Forceps Model/Catalog Number: HACF0533 Product Description: The HALO PKS Cutting Forceps are intended to be pasOlympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.
- Class II
Medical Device Recall · February 25, 2026
Medline Kits: 1) SYR CNTRL 10ML RING W/ROT NB, Model Number: DYNJSYR10CWRB; 2) MANIFOLD KIT LOW PRESSURE OFF, Model Number: VASCSLPOFF1; 3) EP MANIFOLD KIT, Model Number: VASC1018AThe 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.