Safety Recalls

17,395 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 401–450 of 17,395

• Drug Recall · August 6, 2026

  ACCORD HEALTHCARE, INC.

  Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Ro

  Subpotent Drug

  Class II

• Medical Device Recall · August 6, 2026

  Boston Scientific Corporation

  LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS ANZ, Model Number 7248, All Versions (Current 7.7)

  There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Burden Alert may delay clinical evaluation or therapeutic intervention of an atrial arrhythmia.

  Class II

• Drug Recall · August 6, 2026

  ACCORD HEALTHCARE, INC.

  Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Ro

  Subpotent Drug

  Class II

• Consumer Product Recall · August 6, 2026

  Louisville Ladder, Inc., of Louisville, Kentucky

  Louisville, Featherlite, Lite & Century Attic Stairway Ladders with gas struts

  The bolts on the attic stairway ladders can break while in use, posing a risk of serious injury or death from fall hazard.

  Unclassified

• Consumer Product Recall · August 6, 2026

  OKK Trading, Inc., of Vernon, California

  Easter LED Headbands

  The recalled headbands violate the mandatory safety standard for toys with button cell and coin batteries because the lithium coin batteries can be accessed easily by children, posing an ingestion hazard. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.

  Unclassified

• Consumer Product Recall · August 6, 2026

  Shenzhen Yuejia Mei Maoyi Youxian Gongsi (Shenzhen Yuejia Mei Trading Co., Ltd.), doing business as BUSOHA, of China

  BUSOHA Magnetic Fidget Slider Toys

  The magnetic fidget sliders violate the mandatory standard for toys because they can liberate 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 · August 6, 2026

  Courant, of Angers, France

  Courant Spliced Kalimba Climbing Ropes

  The spliced termination ends on the recalled ropes can fail unexpectedly, posing a risk of serious injury or death from fall hazard.

  Unclassified

• Drug Recall · August 6, 2026

  ACCORD HEALTHCARE, INC.

  Levothyroxine Sodium Tablets, USP, 100 mcg (0.1 mg), packaged in a) 90-count bottles (NDC 16729-451-15) and b) 1000-count bottles, (NDC 16729-451-17), Rx Only, Manufactured for: Accord Healthcare, Inc

  Subpotent Drug

  Class II

• Consumer Product Recall · August 6, 2026

  Generac Power Systems Inc., of Waukesha, Wisconsin

  DR Power PRO MAX30 30" Walk-Behind Power Lawn Mowers

  The recalled mowers violate the mandatory safety standard for walk-behind power lawn mowers because the blades can operate without the blade control system engaged or continue to operate even after the release of the control, posing a serious laceration hazard.

  Unclassified

• Consumer Product Recall · August 6, 2026

  Vanderhall North America, LLC, of Provo, Utah

  Vanderhall Brawley GTS electric recreational off highway vehicles

  The recalled recreational off highway vehicle can maintain speed or accelerate when the accelerator pedal is released, posing a risk of serious injury or death from a crash hazard.

  Unclassified

• Consumer Product Recall · August 6, 2026

  Senyu Era International Co. Limited, dba Syera, of China

  Space Astronaut LED Finger Lights

  The recalled LED finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.

  Unclassified

• Consumer Product Recall · August 6, 2026

  Changsha 678 Trading Co., Ltd., dba Luqiba, of China

  Liuqibax Adult 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

• Drug Recall · August 6, 2026

  ACCORD HEALTHCARE, INC.

  Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Ro

  Subpotent Drug

  Class II

• Consumer Product Recall · August 6, 2026

  EEMB USA, doing business as A2batt, Inc., of Redlands, California

  EEMB Lithium-ion Coin Battery Chargers with Rechargeable 2032 Batteries

  The recalled battery chargers violate the mandatory standard for consumer products containing button cell or coin batteries, because the charger has lithium coin batteries that can be accessed easily by children. In addition, the coin batteries provided with the battery charger are not in child-resistant packaging, and the packaging does not have the warnings, as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

  Unclassified

• Consumer Product Recall · August 6, 2026

  Fitueyes, Inc., of City of Industry, California

  Laziza 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 standard as required by the STURDY Act.

  Unclassified

• Consumer Product Recall · August 6, 2026

  HEAD USA, Inc. dba Head Watersports of Delray Beach, Florida

  Apeks Second Stage Scuba Regulators

  The recalled second stage regulators can restrict air flow to the user at depths exceeding 45 meters (approximately 147 feet), posing risk of serious injury or death from a drowning hazard.

  Unclassified

• Consumer Product Recall · August 6, 2026

  KC IMPORTS AND EXPORTS, Inc., of Vernon, California

  Laser & LED Light Mini Laser Pointer Keychains

  The Mini Laser Pointer Keychains violate the mandatory safety standard for consumer products with button cell and coin batteries because the button batteries can be accessed easily by children, posing an ingestion hazard. Additionally, the packaging and product do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

  Unclassified

• Consumer Product Recall · August 6, 2026

  Shenzhen Okabesini Technology Co., Ltd., dba Okabesini-us, of China

  Little Rawr Silicone 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 a deadly choking hazard.

  Unclassified

• Consumer Product Recall · August 6, 2026

  Shanghaiyuejiuyaoguojimaoyiyouxiangongsi (Shanghai Yuejiuyao International Trade Co., Ltd.), dba Voomf, of China

  Voomf Play Yard and Crib Mattresses

  The recalled mattresses violate the mandatory safety standard for crib mattresses because the mattresses may not adequately fit certain play yards, posing a deadly entrapment hazard. Babies can suffocate in gaps between an undersized mattress, or extra padding, and side walls of a product, especially when the infant's face becomes trapped against the side and the mattress, preventing the infant from breathing. Furthermore, the full-sized crib mattresses violate the mandatory flammability standard for mattress sets, posing a risk of serious injury or death from fire.

  Unclassified

• Consumer Product Recall · August 6, 2026

  Changsha Yuelu District Ruiwu E-Commerce Co., Ltd., dba WURUI.BABY, of China

  Wnttmt Baby Walkers

  The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a deadly fall hazard. In addition, the infant walkers have leg openings that allow the child to slip down until the child's head can become entrapped, posing a risk of serious injury or death.

  Unclassified

• Drug Recall · August 6, 2026

  Baxter Healthcare Corporation

  Vasopressin, in 0.9% Sodium Chloride Injection, 40 units per 100 mL (0.4 units/mL), 100mL Single-Dose Container, Rx only, Sterile, Baxter Healthcare Corporation, Deerfield, IL, 60015 USA, NDC 0338-964

  CGMP Deviations

  Class II

• Vehicle Recall · August 6, 2026

  Rivian Automotive, LLC

  2025 RIVIAN R1T, 2025 RIVIAN R1S

  Turn signals that do not function properly increase the risk of a crash.

  Unclassified

• Drug Recall · August 6, 2026

  Baxter Healthcare Corporation

  Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg per 100 mL (10 mg/mL), 1,000 mg total, in 1000 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield

  CGMP Deviations

  Class II

• Drug Recall · August 6, 2026

  Baxter Healthcare Corporation

  Clindamycin Injection USP in 5% Dextrose, 900 mg/50 mL (18 mg/mL), in GALAXY 50 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Manufactured by: Baxter Healthcare Corporation, Deerfield, IL 6

  CGMP Deviations

  Class II

• Drug Recall · August 6, 2026

  Baxter Healthcare Corporation

  Nexterone (amiodarone HCI), 360 mg/200 mL (1.8 mg/mL) in GALAXY Single-Dose Container, sterile, Nonpyrogenic, iso-osmotic solution in Dextrose, Baxter Healthcare Corporation, Deerfield, IL 60015, Made

  CGMP Deviations

  Class II

• Drug Recall · August 6, 2026

  ACCORD HEALTHCARE, INC.

  Levothyroxine Sodium Tablets, USP, 50 mcg (0.05 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Roa

  Subpotent Drug

  Class II

• Drug Recall · August 6, 2026

  ACCORD HEALTHCARE, INC.

  Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp R

  Subpotent Drug

  Class II

• Medical Device Recall · August 6, 2026

  Boston Scientific Corporation

  LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS US, Model Number 7260, All Versions (Current 7.8)

  There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Burden Alert may delay clinical evaluation or therapeutic intervention of an atrial arrhythmia.

  Class II

• Medical Device Recall · August 6, 2026

  Lutronic Corporation

  Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that delivers pulsed laser energy at wavelengths of 532 nm and 1064 nm through a fiber-optic handpiece. The syst

  Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in patient burn.

  Class II

• Drug Recall · August 6, 2026

  Baxter Healthcare Corporation

  Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) in Galaxy 100 mL Single Dose Container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA,

  CGMP Deviations

  Class II

• Drug Recall · August 6, 2026

  ACCORD HEALTHCARE, INC.

  Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Ro

  Subpotent Drug

  Class II

• Drug Recall · August 6, 2026

  Mallinckrodt Hospital Products Inc.

  Acthar Gel (repository corticotropin injection), 5 mL multiple-dose vial, Rx Only, Mfd. for: Mallinckrodt ARD LLC, Bridgewater, NJ 08807, NDC 63004-8710-1 & NDC 63004-8710-2

  Presence of particulate matter: glass and stopper piece

  Class II

• Drug Recall · August 6, 2026

  Baxter Healthcare Corporation

  Vancomycin Injection, USP, in 0.9% Sodium Chloride, 1g per 200 mL (5 mg/mL) in GALAXY Single-Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL, 60015 USA, NDC

  CGMP Deviations

  Class II

• Drug Recall · August 6, 2026

  Baxter Healthcare Corporation

  Clindamycin Injection USP in 5% Dextrose, 900 mg/50 mL (18 mg/mL), in GALAXY 50 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Manufactured by: Baxter Healthcare Corporation, Deerfield, IL 6

  CGMP Deviations

  Class II

• Food Recall · August 6, 2026

  Ron's Home Style Foods, Inc.

  Item #DIPSAU0205RFS Salsa Autentica 5 lb. packaged in round plastic container.

  Products were manufactured with jalapenos that have the potential to be contaminated with Salmonella

  Class I

• Drug Recall · August 6, 2026

  Baxter Healthcare Corporation

  Clindamycin Phosphate in 0.9% Sodium Chloride Injection, 600 mg per 50 mL (12 mg/mL), 50 mL Single-Dose GALAXY Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60

  CGMP Deviations

  Class II

• Food Recall · August 6, 2026

  Ron's Home Style Foods, Inc.

  Item # DIPPIC0205RFS Pico de Gallo 5 lb packaged in round plastic container.

  Products were manufactured with jalapenos that have the potential to be contaminated with Salmonella

  Class I

• Food Recall · August 5, 2026

  NatureBest Pre-Cut & Produce LLc

  HEB-PICO-MANGO-12/14oz PICO DE GALLO-MANGO-4/14oz PICO DE GALLO-MANGO-6/14oz

  Jalapenos have the potential to be contaminated with Salmonella

  Class I

• Drug Recall · August 5, 2026

  Zydus Pharmaceuticals (USA) Inc

  Mirabegron Extended-Release Tablets, 25 mg, 30-count bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Matoda, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington,

  CGMP: Due to Out of Specification (OOS) result for N-Nitroso Mirabegron impurity.

  Class II

• Medical Device Recall · August 5, 2026

  Nipro Renal Soultions USA, Corporation

  Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D,LC+201, LC+225(45X)

  Hemodialysis concentrates contain high endotoxin levels

  Class II

• Vehicle Recall · August 5, 2026

  Tesla, Inc.

  2023 TESLA MODEL 3

  Headlight low beams that are too bright can reduce visibility for oncoming drivers, increasing the risk of a crash.

  Unclassified

• Food Recall · August 5, 2026

  NatureBest Pre-Cut & Produce LLc

  PEPPER-JALAPENO-DC 1/4"-4/5# PEPPER-JALAPENO-DC 1/4"-1/5# PEPPER-JALAPENO-SL 1/8"-1/5# PEPPER-JAL/SER-MINCE W/SD-6/5# PEPPER-JALAPENO-DC 3/8"-4/5# PEPPER-JALAPENO-DC 1/8"-BG-10# Pepper Jalapeno Destem

  Jalapenos have the potential to be contaminated with Salmonella

  Class I

• Food Recall · August 5, 2026

  Jaime's Foods ATX, LLC

  Jalapeno Ranch, packed in 16 oz. glass jars, 6 jars per case, with UPC #199284564923.

  Undeclared Egg Allergen

  Class I

• Food Recall · August 5, 2026

  NatureBest Pre-Cut & Produce LLc

  PICO DE GALLO-HOT-6/9oz HEB-PICO-HOT-12/14oz

  Jalapenos have the potential to be contaminated with Salmonella

  Class I

• Food Recall · August 5, 2026

  Dairyland Produce, LLC

  Dairyland Produce, LLC Pepper Jalapeno, repackaged into the following sized clear plastic bags: 1. 1 lb., item number 01213, UPC 0009907729 2. 3 lbs., item number 02611, UPC 0009902703; 3.

  Jalapenos may be contaminated with Salmonella.

  Class I

• Food Recall · August 5, 2026

  Marina Del Rey Foods inc.

  Frankie's Organic Plant-Based Puffs Vegan Cheddar, NET WT. 4 oz. (113 g). Product is packaged into flexible plastic bag, UPC 816929000119. Sold wholesale: 12 retail units/ case

  Product tested positive for undeclared milk.

  Class I

• Medical Device Recall · August 5, 2026

  Nipro Renal Soultions USA, Corporation

  Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25

  Hemodialysis concentrates contain high endotoxin levels

  Class II

• Drug Recall · August 5, 2026

  OPTIMAL BALANCE PHARMACY

  Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid, Benzyl Alcohol & sterile water for injection, For IM or IV Injection Use Only, RX only, Optimal Ba

  Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.

  Class I

• Medical Device Recall · August 5, 2026

  Nipro Renal Soultions USA, Corporation

  MedicaLyte Bicarbonate Powder REF: DB+201-2.1(45X) and DB+201-25 (35X, 36.83X, 45X))

  Hemodialysis concentrates contain high endotoxin levels

  Class II

• Food Recall · August 5, 2026

  NatureBest Pre-Cut & Produce LLc

  NatureBest Mild Cheddar & Jalapeno Stuffed Mushrooms 8oz (227g) HEB SI JAL POP STFFD MUSHRM-6/8oz

  Jalapenos have the potential to be contaminated with Salmonella

  Class I