Safety Recalls

15,062 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 51–100 of 15,062

• Consumer Product Recall · June 25, 2026

  Kith Retail Inc. of Brooklyn, New York

  Kids Kithmas Plaid Lounge Sets

  The recalled children's loungewear sets violate the mandatory flammability standards for children's sleepwear, posing a risk of serious burn injuries.

  Unclassified

• Consumer Product Recall · June 25, 2026

  Shield Line LLC, of Branchburg, New Jersey

  MedPride Baby Oil

  The baby oil contains low-viscosity hydrocarbons, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The baby oil's packaging is not child-resistant, posing a risk of serious injury or illness from poisoning if the contents are swallowed by young children. Additionally, petroleum distillates can get into the lungs, causing chemical pneumonia and/or pulmonary damage, which can be fatal.

  Unclassified

• Consumer Product Recall · June 25, 2026

  Lesonic Technology Co., Ltd., dba Small Fish, of China

  Small Fish Montessori Busy Board Toys

  The busy boards violate the mandatory safety standard for toys because magnets can detach, posing a deadly ingestion hazard. 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

• Drug Recall · June 22, 2026

  Direct Rx

  DULOXETINE D/R, a) 30 mg (NDC 61919-482-30), 30 Caps; b) 30 mg (NDC 61919-482-60), 60 Caps; CYMBALTA, Packaged and Distributed by Direct Rx.

  CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit

  Class II

• Consumer Product Recall · June 18, 2026

  CooCooBaby, of China

  CooCooBaby Baby Loungers

  The baby loungers violate the mandatory standard for Infant Sleep Products because the sides are shorter than the minimum side height limit to secure the infant; the sleeping pad's thickness exceeds the maximum limit, posing a suffocation hazard; and an infant could fall out of an enclosed opening at the foot of the lounger or become entrapped. The portable loungers do not have a stand, posing a fall hazard. These violations create an unsafe sleeping environment for infants, posing a risk of serious injury or death.

  Unclassified

• Consumer Product Recall · June 18, 2026

  Huizhou Huitong Crafts Co. Ltd., of China

  BABESIDE Doll and Stroller Toys

  The recalled toys violate the small parts ban because they are intended for children under three and the small pacifier poses a deadly choking hazard to young children. In addition, the eyes on the plush bear can detach, also posing a choking hazard.

  Unclassified

• Consumer Product Recall · June 18, 2026

  GOPO Toys LLC, of San Bernardino, California

  GOPO TOYS Pull String Teething Toys

  The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach the back of children's throat and become lodged, posing a serious risk of respiratory distress and deadly choking hazard.

  Unclassified

• Consumer Product Recall · June 18, 2026

  SHEIN Distribution Corporation, of Los Angeles, California

  Michley Children's Pajamas

  The recalled children’s pajamas violate the mandatory flammability standard for children’s sleepwear, posing a risk of serious burn injuries or death.

  Unclassified

• Consumer Product Recall · June 18, 2026

  Shenzhen Fuxiangyue Technology Co., Ltd., dba Arrogantf, of China

  Arrogantf Spa Drain Covers

  The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to consumers.

  Unclassified

• Consumer Product Recall · June 18, 2026

  7111495 Canada Inc., dba Arizer Tech, of Waterloo, Ontario

  Arizer Solo III portable electronic vaporizers (Intergalactic/Black color only)

  The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.

  Unclassified

• Consumer Product Recall · June 18, 2026

  Bada Boom Fireworks, of Blakeslee, Pennsylvania

  Pyro Diablo "Diablo Rising" 9 Shots

  The recalled fireworks violate the ban for aerial fireworks devices intended to produce audible effects because they have a pyrotechnic composition that exceeds the federal limit, posing deadly explosion and burn hazards. Overloaded fireworks can result in a greater than expected explosion.

  Unclassified

• Consumer Product Recall · June 18, 2026

  Joolz USA Inc., of New York, New York

  Joolz Aer2 Car Seat Adapters for Joolz Aer 2 Stroller

  The recalled car seat adapters can fail to properly attach to the stroller, which may allow the car seat to fall, posing a risk of serious injury from a fall hazard.

  Unclassified

• Consumer Product Recall · June 18, 2026

  Shenzhen City ShengRu Fu Shi Company Ltd., doing business as Veseacky, of China

  Veseacky Pajama Sets

  The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.

  Unclassified

• Drug Recall · June 17, 2026

  SUN PHARMACEUTICAL INDUSTRIES INC

  Perampanel CIII Tablets, 6mg, Rx only, 30 Tablets, Mfd.by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 2624761, Dist. by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 51672-

  Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets.

  Class II

• Drug Recall · June 16, 2026

  The Harvard Drug Group LLC

  Carton Label: MAJOR, Methylergonovine Maleate Tablets, USP, 0.2 mg, 20 TABLETS (2 x 10), Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, in 46268, NDC 0904-7282-10. Blister

  Subpotent Drug

  Class II

• Drug Recall · June 12, 2026

  Par Health USA, LLC

  Buprenorphine HCl, CIII, Injection, 0.3 mg/mL, 5 x 1 mL Single Dose Vials per Carton, Rx Only, For Intramuscular or Intravenous use, Manufactured for: Endo USA, Malvern, PA 19355, NDC 42023-179-05

  Crystallization; identified as Buprenorphine free base

  Class II

• Consumer Product Recall · June 11, 2026

  Guangzhou Huanmao Business Service Co. Ltd., of China

  LiKee Pull String Teething Toys

  The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach the back of children's throat and become lodged, posing a serious risk of respiratory distress and deadly choking hazard.

  Unclassified

• Consumer Product Recall · June 11, 2026

  Foshan Nanhai District Haichen Tengfei Hardware Factory, of China

  Houoto 642-2150V Pool Drain Covers

  The drain covers do not bear the required product markings, in violation of the mandatory safety standard under the?Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing risk of serious injury or death from entrapment and drowning hazards. The drain covers also fail to meet safety requirements because they are missing statements regarding the service life of the covers and installation and maintenance instructions.

  Unclassified

• Consumer Product Recall · June 11, 2026

  Joyin US Corp., of Chandler, Arizona

  Sloosh Dive Sticks

  The recalled dive sticks violate the federal dive sticks ban because they exceeded the compress limit, posing an impalement hazard. In shallow water, children may fall or land on a dive stick, resulting in serious piercing injuries. Facial and eye injuries are also possible when children attempt to retrieve the sticks underwater.

  Unclassified

• Consumer Product Recall · June 11, 2026

  Kawasaki Motors Manufacturing Corp., U.S.A., of Lincoln, Nebraska

  Model Year 2026 Teryx4 H2 and Teryx5 H2 recreational off-road vehicles

  The drive converter sheave can break in certain circumstances, resulting in metal fragments being discharged within the engine compartment and surrounding area, posing impact and injury hazards.

  Unclassified

• Consumer Product Recall · June 11, 2026

  Shenzhen DUOMENGDUO Electronic Commerce Co., Ltd., dba Hasuit Direct, of China

  Hasuit 7-Drawer Dressers

  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 death to children. The dressers violate the mandatory safety standards as required by the STURDY Act.

  Unclassified

• Consumer Product Recall · June 11, 2026

  Jiangsu Zhirun Xiangmu Management Co., Ltd., dba MOCCI SHOP, of China

  Hopelight Adult Portable Bed Rails

  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 rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.

  Unclassified

• Consumer Product Recall · June 11, 2026

  School Specialty, LLC, of Greenville, Wisconsin

  Plastic Tip Restraint Kits

  The recalled plastic tip restraint kits (also referred to as furniture straps) can break or degrade, posing tip-over and entrapment hazards. Should the defective plastic tip restraints break, consumers could be at risk of serious injuries or death. This is a hidden defect because consumers who purchase and install this product may be under a false sense of security that their furniture is safe from a tip-over incident.

  Unclassified

• Consumer Product Recall · June 11, 2026

  Merkury Innovations, of New York, New York

  Hot + Cool Heating and Cooling Fans

  The fan can overheat, posing a risk of serious injury or death from a fire hazard.

  Unclassified

• Consumer Product Recall · June 11, 2026

  The Black Sheep Fam, of Kewaskum, Wisconsin

  Girls' Sleepshirt and Kids' Unisex Jogger Pajama Sets

  The recalled children's pajamas violate the mandatory flammability safety standard for children's sleepwear, posing a risk of serious burn injuries or death to children.

  Unclassified

• Consumer Product Recall · June 11, 2026

  California Innovations Inc., of Canada

  Arctic Zone Titan Pro Coolers

  The recalled coolers' latch magnet can detach, posing risk of serious injury or death from a choking hazard.

  Unclassified

• Consumer Product Recall · June 11, 2026

  HSN, Inc., of West Chester, Pennsylvania

  Kitchen HQ Thermal Insulated Bowls with Detachable Hinged Lids

  Metal springs in the detachable hinged lid of the insulated bowls can catch fire when used in the microwave, posing a fire hazard.

  Unclassified

• Consumer Product Recall · June 11, 2026

  shenzhenshinikezhinengshebeiyouxiangongsi (Shenzhen Nike Intelligent Equipment Co., Ltd.) dba Nimood US, of China

  Nimood Adult Portable Bed Rails

  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 rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. Furthermore, the bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard. In addition, the bed rails do not bear the required hazard warning labels.

  Unclassified

• Consumer Product Recall · June 11, 2026

  Fujian Xiniuniu Home Furnishing Co., Ltd., of China

  Timechee Changing Table Dressers

  The recalled dressers are unstable if not anchored to the wall, posing tip-over and entrapment hazards that can result in a risk of serious injuries or death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.

  Unclassified

• Consumer Product Recall · June 11, 2026

  Yamaha Golf-Car Company, of Kennesaw, GA

  Model Year 2021-2022 Yamaha Drive2 Electric Fleet Golf Cars

  The recalled golf cars' passenger-side brake cable could have been misrouted during assembly. If the cable was misrouted, abnormal wear can occur which can cause the passenger-side cable to break during use, posing a risk of serious injury or death from a crash hazard.

  Unclassified

• Consumer Product Recall · June 11, 2026

  Yamaha Golf-Car Company, of Kennesaw, Georgia

  Model Year 2019-2025 UMAX Bistro and Bistro Deluxe Vehicles

  The recalled Bistro and Bistro Deluxe vehicles have an inaccurate weight capacity certification label. This could result in the vehicle being overloaded, which poses an injury hazard.

  Unclassified

• Consumer Product Recall · June 11, 2026

  ChangShaShiMengQiSiDianZiShangMaoYouXianGongSi, of China

  Kidisle Coffeemakers

  The recalled coffeemakers can become clogged, causing hot liquid or steam to build up and be released unexpectedly during use, posing a risk of serious injury from burn hazard.

  Unclassified

• Food Recall · June 9, 2026

  GREENWORLD FOOD EXPRESS (USA) LLC

  Al Yaman Halawa Extra Pistachio 907g (31.994 oz) plastic jars, UPC 5 287000 098083, 12 retail units per case

  Product may be contaminated with Salmonella

  Class I

• Vehicle Recall · June 7, 2026

  Southeast Toyota Distributors, LLC

  2026 TOYOTA TUNDRA

  An incorrect load carrying capacity modification label may lead to improper loading of the vehicle, increasing the risk of a crash.

  Unclassified

• Drug Recall · June 5, 2026

  Inventia Healthcare Limited

  Chlorthalidone Tablets, USP, 25 mg, [100 or 1000] Tablets pr bottle, Rx only, Manufactured by: Inventia Healthcare Limited, Additional Ambernath, M.I.D.C., Ambernath (East) - 421506, INDIA. Distribut

  Failed Dissolution Specifications

  Class II

• Medical Device Recall · June 5, 2026

  Philips North America Llc

  Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following system descriptions: TELE Monitor 5500, 1.4 Ghz, ECG only, ex; Telemetry Monitor 5500 1.4 GHz FAST EX.

  Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure to reconnect to the PIC iX central monitoring system.

  Class II

• Drug Recall · June 4, 2026

  Amgen, Inc.

  Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC 55513-800-99), and b) 60 tablet bottles (NDC 55513-800-60), Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy.

  Presence of Foreign Substance.

  Class II

• Vehicle Recall · June 4, 2026

  Hyundai Motor America

  2023 GENESIS G90, 2023 HYUNDAI IONIQ 6, 2024 GENESIS G90, 2024 HYUNDAI SANTA FE, 2024 HYUNDAI IONIQ 6, 2025 GENESIS G90, 2025 HYUNDAI SANTA FE, 2025 HYUNDAI IONIQ 6, 2025 HYUNDAI SANTA FE HYBRID, 2026

  A detached seat belt anchor will not adequately restrain the seat occupant, increasing the risk of injury in a crash.

  Unclassified

• Drug Recall · June 4, 2026

  Haleon US Holdings LLC

  Gas-X Extra Strength, SIMETHICONE 125 mg/ANTIGAS, packaged in a) 120 SoftGels (UPC 3 00674 35041 9, b) 72 SoftGels (UPC 3 00439 00572 1), Distributed by: Haleon, Warren, NJ 07059.

  Chemical Contamination: contamination with a diluted propylene glycol-based coolant from a machine leakage during the packaging process.

  Class I

• Drug Recall · June 4, 2026

  Elevate Oral Care

  Povi-One, 10% Povidone-Iodine Oral Antiseptic, Packaged by Elevate Oral Care, LLC, 346 Pike Road, Suite 6, West Palm Beach, FL 33411, NDC 57511-0611-1.

  sub potency

  Class II

• Drug Recall · June 4, 2026

  Annora Pharma Private Limited

  Lacosamide Tablets, USP, C V, 100mg, Rx only, 60-count bottle, By: Annora Pharma Pvt., Ltd, Sangareddy -502313, Telangana, India, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854,

  Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.

  Class II

• Drug Recall · June 4, 2026

  Breckenridge Pharmaceutical, Inc.

  Duloxetine Delayed-Release Capsules, USP, 60mg, packaged in a) 90 Capsules (NDC 51991-748-90); b) 1000 Capsules (51991-748-10), Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelo

  CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit

  Class II

• Drug Recall · June 4, 2026

  Amgen, Inc.

  Corlanor (ivabradine) tablets, 7.5mg, 60-count bottles, Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy. NDC 55513-810-60

  Presence of Foreign Substance.

  Class II

• Drug Recall · June 4, 2026

  Amgen, Inc.

  Sensipar (cinacalcet) Tablets, 60mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks ,CA 91320-1799, Made in Japan. NDC 55513-074-30

  CGMP Deviations

  Class II

• Drug Recall · June 4, 2026

  Amgen, Inc.

  Sensipar (cinacalcet) Tablets, 90mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks, CA 91320-1799, Made in Japan. NDC 55513-075-30

  CGMP Deviations

  Class II

• Consumer Product Recall · June 4, 2026

  XJ Evermore LLC, dba Little Grape Land US, of Frisco, Texas

  Little Grape Land Nursing Pillows

  The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows?and infant support cushions?because they can obstruct an infant's breathing, posing a serious risk of injury or death from suffocation.

  Unclassified

• Consumer Product Recall · June 4, 2026

  SUNS International LLC, of Chelmsford, Massachusetts

  SUNS SS6291 Solenoid Interlock Switches

  The affected interlock switches can become stuck in a retracted position, allowing the exterior door to remain unlocked, posing a risk of death or serious injury if the elevator is called to another floor.

  Unclassified

• Drug Recall · June 4, 2026

  Breckenridge Pharmaceutical, Inc.

  Duloxetine Delayed-Release Capsules, USP, 30mg, 1000 Capsule bottles, Rx only, Manufactured. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Distributed by: Breckenridge Pharmace

  CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit

  Class II

• Consumer Product Recall · June 4, 2026

  TOMY International, Inc., of Oak Brook, Illinois

  Boon NURSH 8 oz Reusable Baby Bottles

  The hard plastic outer shell can bubble or partially peel off, resulting in loose pieces of film-like plastic that pose a choking hazard to young children.

  Unclassified

• Drug Recall · June 4, 2026

  Amgen, Inc.

  Sensipar (cinacalcet) Tablets, 30mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks ,CA 91320-1799, Made in Japan. NDC 55513-073-30

  CGMP Deviations

  Class II