Product Recalls Today
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Track recent product recall alerts from official U.S. sources. Filter by recall date, source agency, risk level and product category to find newly published food, vehicle, baby product, medical device and consumer product recalls.
Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
Scepter Fuel Containers Recalled Due to Risk of Serious Injury or Death from Flash Fire, Burn and Child Poisoning; Violates Mandatory Standards for Portable Fuel Containers; Imported by Mameix Retail
This recall involves Scepter B62 gas and oil fuel containers. The recalled combination fuel containers are red with black caps and yellow spouts on each end. They have dual chambers with a 6-liter gas capacity on one side and 2.5-liter oil capacity on the other. "Scepter" and "Essence Danger" are embossed on the side of the container.
|
CPSC
10603
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 4, 2026
|
Details |
Zan International Trading Recalls Lotus Joy Sweet Birch Essential Oil Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
This recall involves Lotus Joy Organic Sweet Birch Essential Oil bottles. The essential oil comes in 0.34 fluid ounce amber bottles with a black cap and a separate glass dropper with a black cap. The white label on the bottle has orange and black text with "LotusJoy", "organic", "sweet birch", "essential oil and "betula lenta" printed on the front and ingredients and directions on the back. The packaging box is blue and has the same information as the front of the bottle in orange and black lettering and has directions and the distributor's information on the back.
|
CPSC
10590
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
YITA Recalls Multiple Brands of Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
This recall involves the five different brands of YITA dressers: Dextrus, ModFusion, Uforic, Yintatech and Yitahome. The 16-drawer dressers were sold in gray, black, white, pink and brown. They have a black or white metal frame, a wooden top and collapsable fabric drawers; and measure about 37.4 inches long, 11.8 inches wide and 57.1 inches tall. SKU numbers FTBFSD-0161, FTBFSD-0162, FTBFSD-0212, FTBFSD-0246 or SKU FTBFSD-0465 is printed on labels located on the dresser's top panel and on the product packaging. The brand name can be found on the product online listing.
|
CPSC
10602
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
Shintenchi 6-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
This recall involves Shintenchi-branded dressers. The recalled, white dressers have six wooden drawers and golden metal feet and measure about 15.7 inches deep by 47.2 inches wide by 30.5 inches high. "SHX12077-WH" is embossed on the underside of the dresser at the top of one metal foot and on the product packaging.
|
CPSC
10591
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
Semfri Children's Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
This recall involves Semfri-branded children's multi-purpose helmets. The recalled helmets were sold in size medium (M), fitting a head circumference of about 20.5 to 22.8 inches; and in the following colors: orange, black, blue, navy blue, pink, red and white. All helmets have black padding, black straps and a black buckle. The helmets have a black plastic knob at the back of the helmet for adjusting the fitting. The size is printed on a black circular label located inside of the helmet.
|
CPSC
10592
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
Organic Zing Birch Essential Oil Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Linkers
This recall involves Organic Zing Birch Oil bottles. The recalled essential oil's amber bottles have black continuous thread caps and a beige and green label with white and black labeling. The Organic Zing logo, "Birch Oil" and "Pure & Natural" are printed on the front of the bottle. The Organic Zing logo and "Pure & Natural" are printed on the front of the bottles' beige and green box packaging and "Made in India" on the back.
|
CPSC
10595
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
Lola Plus The Boys Recalls Youth Clothing with Drawstrings Due to Risk of Serious Injury or Death from Strangulation Hazard; Violates Federal Rule for Children's Upper Outerwear
This recall involves five styles of Lola + The Boys hooded clothing with drawstrings: -The Candy Heart Tie Dye set consists of pink and white pants and a sweatshirt. Both have a yellow drawstring with beads, and the sweatshirt has a heart on the front. -The Hoodie Unicorn Tutu set consist of a rainbow organza skirt and a purple hoodie sweatshirt with a unicorn on the front. -The Justice League Hero hoodie is gray and has a front pocket and superhero decals along the right sleeve. -The Emoji Love hoodie sweatshirt is white and has a pocket and three smiley emojis on the front. -The Crystal Rainbow Rain hoodie is gray and has a front pocket and rainbow-colored beads at both ends of the drawstrings. The clothing was sold in youth sizes 1 through 12. "Lola + The Boys" and the size are printed on the neck label.
|
CPSC
10593
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
Kitosun Submersible LED Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries
This recall involves Kitosun Submersible LED Lights. The LED lights include 10 color-changing LED lights, two remote controls, 20 preinstalled CR2450 lithium batteries in the lights and four preinstalled CR2032 lithium batteries in the remote controls. Each light is about 3.5 cm in diameter. Note: Button cell and coin batteries are hazardous. Batteries should be disposed of or recycled by following local hazardous waste procedures.
|
CPSC
10597
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
GM Gumili Wintergreen Essential Oil Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Gumili Beauty
This recall involves GM Gumili Wintergreen Essential Oil. The essential oil was sold in an amber glass bottle with a black screw-on cap and a white label with the "GM" logo, "gumili," "wintergreen essential oil" and an image of a wintergreen plant. The packaging box is white with blue text with the "GM" logo, "gumili," "essential oil" and "100% pure & natural" on the front. The back of the box has directions, safety instructions and the manufacturer's information. A black dropper cap was included with the oil.
|
CPSC
10596
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
Furnulem 5-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates Mandatory Standard for Clothing Storage Units
This recall involves Furnulem five-drawer dressers. The wooden, white dressers measure about 31.5 inches tall, 15.75 inches long and 50.2 inches wide. They have a top with recessed power outlets, and each drawer has two round pull knobs. Only dressers that did not come with feet extensions are included in this recall. Model "HK-DS-017-CL-5D-1-W" is printed on the packaging.
|
CPSC
10598
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
Fixwal 7-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
This recall involves the Fixwal 7-Drawer Dressers. The recalled dressers were sold in black and white and have a metal frame, wooden top, and seven collapsable fabric drawers. The dressers are 55.1 inches long by 11.8 inches wide by 31.5 inches tall.
|
CPSC
10599
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
EnHomee 10-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
This recall involves EnHomee 10-Drawer Dressers. The recalled dressers were sold in the following colors: black, white, grey, and brown. They have a metal frame, wooden top, 10 collapsable fabric drawers, and two metal drawers. The dressers are 38 inches long by 11.8 inches wide by 48.1 inches tall. Model number "55SCWMSCXLBR" can be found on the order information within your Amazon account.
|
CPSC
10606
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
Dresbe LED Christmas Headbands Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
This recall involves Dresbe LED Christmas Headbands. The headbands were sold as a two-pack of novelty headbands, one red headband with candy cane attachments and a green headband with a Christmas tree attachment, each containing three button cell batteries to power LED lights. The headbands have "HB-052" and "DRESBE LED Christmas Headband (2pc)" printed on labels located on the package.
|
CPSC
10600
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
Cobelae Busy Books Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violates Small Parts Ban; Sold on Amazon by Flyindream
This recall involves Cobelae Busy Book, model: 2025-Q3-0702. The Busy Book has a yellow and brown giraffe on the front cover. The apple on page eight of the books includes a string of beads. There are no markings on the book.
|
CPSC
10605
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
Andy & Evan Recalls Children's Pajama Sets Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Children's Sleepwear
This recall involves Andy & Evan-branded children's pajama sets. The recalled woven pajamas consist of a long-sleeved shirt with buttons, a front pocket and matching flared pants. The pajamas were sold in pink with white stripes and purple and pink hearts with trim in children's sizes 2T, 3T, 4T, 5, 6 and 6X. "Andy & Evan" and the size are printed on the sewn-in neck label. "RN# 136762" and "YC05" are printed on the sewn-in side seam label.
|
CPSC
10607
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
|
BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The BD AlarisTM System with Guardrails" Suite MX is a modular infusion pump and monitoring system for the continuous or intermittent administration of fluids to adult, pediatric, and neonatal patients through clinically accepted routes of administration: intravenous (IV), intra-arterial (IA), subcutaneous, epidural, or irrigation of fluid spaces. The BD AlarisTM System includes the PC Unit (PCU) and one or more of the following: Pump Module, Syringe Module, end-tidal CO2 (EtCO2) Module, Auto-ID Module, patient-controlled analgesia (
Due to a number of modules flashed with a date and time associated with the daylight savings time (DST) adjustment that may cause connectivity issue with hospital networks. This issue only affects the Interoperability workflow for devices with a DST invalid timestamp, impacting connectivity of the PCU to the hospital network
|
FDA
Z-1217-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Nov 6, 2025
|
Details |
|
Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK, Kit SKU DYNJ16826O
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
|
FDA
Z-1198-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 12, 2025
|
Details |
|
Brand Name: Elekta Medical Linear Accelerator Product Name: Elekta Synergy, Elekta Harmony, Elekta Infinity, Versa HD Software Version: N/A Product Description: Digital Linear Accelerator Component: No
Due to a manufacturing issue and electrical grounding of systems.
|
FDA
Z-1164-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 14, 2025
|
Details |
|
Conductivity Standard Solution Catalog/Model Numbers: 10001, 10011, 10021, 10032, 10040, 10040c, and 10041 Conductivity Standard Solutions are a secondary standard solution used for the calibration of conductivity cells together with conductivity meters
due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values for dialysate.
|
FDA
Z-1185-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 12, 2025
|
Details |
|
Alphenix INFX-8000C, interventional fluoroscopic x-ray system
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
|
FDA
Z-1176-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 19, 2025
|
Details |
|
Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS, Kit SKU CDS984347O; 2) HEAD AND NECK CDS-LF, Kit SKU CDS984857N; 3) NECK PACK-LF, Kit SKU DYNJ0966130K; 4) NECKLINE PACK-LF, Kit SKU DYNJ51440B; 5) THYROID PACK, Kit SKU DYNJ58742J; 6) ENT I, Kit SKU DYNJ63781B; 7) NECK PACK, Kit SKU DYNJ82751B; 8) NOSE PACK, Kit SKU DYNJ82753C; 9) WMC COCHLEAR IMPLANT ADD ON, Kit SKU DYNJ907206G.
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
|
FDA
Z-1190-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 12, 2025
|
Details |
|
Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT
Potential exposure of rodents and rodent activity in the distribution center.
|
FDA
Z-1180-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 26, 2025
|
Details |
|
Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF, Kit SKU DYNJ0660040R; 2) PLASTICS VCH, Kit SKU DYNJ39225K; 3) WT BREAST PACK, Kit SKU DYNJ46620I; 4) ENDO / AUG PACK, Kit SKU DYNJ59250I; 5) KMC PLASTIC/GEN PACK-LF, Kit SKU DYNJ65980J; 6) PLASTICS PACK, Kit SKU DYNJ68288A; 7) IMPLANT REMOVAL KIT, Kit SKU MNS13035; 8) PLASTICS PACK-LF, Kit SKU PHS41746D.
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
|
FDA
Z-1192-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 12, 2025
|
Details |
|
Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700REA Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Component: No
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
|
FDA
Z-1114-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 15, 2025
|
Details |
|
Ingenia 1.5T. Product Code (REF): (1) 781341, (2) 781396. MR systems with SW version R11.1 and R12.1.
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
|
FDA
Z-1206-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 3, 2025
|
Details |
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
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