Safety Recalls

15,768 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 101–150 of 15,768

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-711-0

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-821-01

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-810-01

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Drug Recall · July 29, 2026

  Prestige Brands Holdings

  CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Company. NDC: 67172-999-01 UPC

  Lack of assurance of sterility. The recall is due to potential contamination

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 20mg (5mg/mL), Glycine 20 mg (5mg/mL), 4 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-724-04.

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-722-02

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-822-02

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-812-03

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Drug Recall · July 29, 2026

  Apollo Care, LLC

  SEMAGLUTIDE 5mg (1mg/mL), Glycine 25 mg (5mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202.NDC 71170-712-03

  Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

  Class II

• Food Recall · July 29, 2026

  Kerry, Inc

  KC Everyday Mac & Cheese, 3lb x 6. Item # 20609055. 6 - 3 lb pouches, Net Wt: 18 lb. (8.16Kg). Fully Cooked. Keep Frozen. Distributed By: Kerry Inc, Beloit, WI 53511.

  Undeclared allergen (egg)

  Class I

• Food Recall · July 28, 2026

  FlavorsandColor.Com

  Honeyville YELLOW COLOR 1 GALLON NFI: WATER, FD&C YELLOW #5, FD&C YELLOW #6, CITRIC ACID, AND SODIUM BENZOATE. MANUFACTURED FOR: HONEYVILLE, INC. RANCHO CUCAMONGA, CA 91730

  Undeclared Red #40.

  Class III

• Food Recall · July 24, 2026

  Big Way Ca Inc

  Big Way Hot Pot "Hot Pot Miso Paste"; 1kg (35.3oz) unit package. Product is packaged in generic bulk packaging.

  Undeclared milk from lactose.

  Class II

• Consumer Product Recall · July 23, 2026

  Foshanshi Kaijinying Dianzishangmao Youxiangongsi (Foshan Kaijinying Electronic Commerce Co., Ltd.), dba YouRfocus, of China

  CuddleCubs Creations Baby Highchair Teething Toy Sets

  The recalled teething toy sets contain a pull string teething toy that violates the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach the back of a child's throat and become lodged, posing a risk of respiratory distress and a deadly choking hazard.

  Unclassified

• Consumer Product Recall · July 23, 2026

  Shenzhen Aojieni Silicone Technology Co., LTD., of China

  Sili Factory 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

• Food Recall · July 23, 2026

  SHEANDRO LLC

  Vodka Tomato Sauce, NET WT. 24 oz / 680g, glass jar packed 12 jars in a carton.

  Label declares cream and cheese, but Milk is not declared

  Class II

• Consumer Product Recall · July 23, 2026

  Xuzhou Mingquanhe Household Co., Ltd., of Changzhou Jiaxuan Intelligence Furniture Co., Ltd., of China

  Romorgniz 12-Drawer Fabric 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 · July 23, 2026

  Xuzhou Mingquanhe Household Co., Ltd., of China

  EnHomee 9-Drawer Fabric Dressers

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

  Unclassified

• Consumer Product Recall · July 23, 2026

  Peony Design Co., of Howell, MI

  Personalized Baby Bibs and Stroller Bags

  The snap can detach from the recalled bibs and stroller bags, posing a risk of serious injury or death from a choking hazard to young children.

  Unclassified

• Drug Recall · July 23, 2026

  Aurobindo Pharma USA Inc

  Dicyclomine Hydrochloride Capsules, USP, 10mg, 1,000 bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India, NDC 59651-719-9

  shortfill; reports of empty capsules.

  Class II

• Drug Recall · July 23, 2026

  Glenmark Pharmaceuticals Inc., USA

  Azelaic Acid Gel, 15%, 50 gram tubes, For Topical Use only, Rx only, Distributed by: Glenmark Pharmaceuticals Inc., USA, Elmwood Park, NJ 07407, NDC 68462-626-52.

  CGMP Deviations: Product quality complaints concerning abnormal texture or consistency (described as grainy, gritty, or sandy) were received.

  Class II

• Consumer Product Recall · July 23, 2026

  Shenzhen Yuanxinxiang Trade Co., Ltd., dba Yuanxinxiang, of China

  OeyUoc Pool Drain Covers

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

  Unclassified

• Consumer Product Recall · July 23, 2026

  Shenzhen Meilanxiang Trading Co., Ltd., dba Sviyatp, of China

  Sviyatp Pool Drain Covers

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

  Unclassified

• Drug Recall · July 22, 2026

  MICRO LABS USA INC

  Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP, 2%/0.5%, 10mL - bottle, Rx only, Manufactured by: Micro Labs Limited, India, Manufactured for: Micro Labs USA Inc., Somerset, NJ 08873. ND

  Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.

  Class II

• Food Recall · July 22, 2026

  MIDWEST POULTRY SERVC C/O H & LELECTRIC

  Grade A Brown In-shell Chicken eggs packaged in the following configurations: 1. Simple Truth, Natural Cage Free Grain Fed, Medium, 12 Eggs, Net Wt 21 oz (1lb 5oz) 596g, UPC 0 11110-87032 0. Distr

  Possible Salmonella Enteritidis

  Class I

• Food Recall · July 22, 2026

  MIDWEST POULTRY SERVC C/O H & LELECTRIC

  Grade A White In-shell Chicken eggs packaged in the following configurations: 1. Kroger, Medium, 12 Eggs, Net Wt 21 oz (1lb 5oz) 596g, UPC 0 11110-60902 1. Distributed by The Kroger Co., Cincinnat

  Possible Salmonella Enteritidis

  Class I

• Food Recall · July 19, 2026

  FACTORY6, INC.

  Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. Intended Use: take 2 capsules per day. Route of Administration: OraI. Manufactured for

  Possible Salmonella in Moringa Leaf Powder product.

  Class I

• Food Recall · July 18, 2026

  M.G. Foods, Inc.

  Spicy Breakfast Burrito sold under the following brand names: FRESH & READY FOODS Spicy Breakfast Burrito Net Wt. 8.2 oz (232g) UPC 1 00001 00029 7 and Sprig & Sprout Spicy Breakfast Burrito IN A SPIC

  Undeclared Soy. The firm received complaints of sausage in the burritos. Upon review the firm discovered the sausage contains soy which is not listed on the label.

  Class I

• Drug Recall · July 17, 2026

  Sunny Pharmtech Inc.

  Cyclophosphamide for Injection, USP, 2 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8114-1

  Presence of Particulate Matter; identified as stainless steel

  Class I

• Drug Recall · July 17, 2026

  Sunny Pharmtech Inc.

  Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8112-1

  Presence of Particulate Matter; identified as stainless steel

  Class I

• Medical Device Recall · July 17, 2026

  Remel Europe Ltd.

  Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL, Product Number R30166901; invitro diagnostics

  Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds.

  Class II

• Medical Device Recall · July 16, 2026

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222,722223, 722224, 722225, 722226, 722227, 722228, 722280*, 722281*, and 722282* (*These models ar

  Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate treatment and 2) Potential loss of geometry movements that may lead to delay of therapy and procedural complications

  Class II

• Consumer Product Recall · July 16, 2026

  Currey & Company, of Atlanta, Georgia

  Nottaway Chandelier Fixtures

  The recalled chandeliers lack proper electrical grounding, posing a risk of serious injury or death from electrocution hazard.

  Unclassified

• Consumer Product Recall · July 16, 2026

  Huish Outdoors, LLC, of Salt Lake City, Utah

  Hollis 200LX Second Stage Diving Regulators

  The regulator inlet tube can crack and break, posing a risk of serious injury or death from drowning.

  Unclassified

• Consumer Product Recall · July 16, 2026

  Shenzhen Gudebo Technology Co. Ltd., of China

  Liizousuda Paint Thinner

  The paint thinner contains low-viscosity petroleum distillates, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The bottles are not child-resistant, posing a risk of serious injury or death 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 · July 16, 2026

  Warren James, Inc., of Santa Monica, California

  Space King No Girls Allowed Relic Lunch Boxes (Cups only)

  The cup in the lunch boxes contains high lead concentration levels for drinking vessels, posing a lead poisoning hazard. Lead is toxic if ingested by adults or children and can cause adverse health issues.

  Unclassified

• Consumer Product Recall · July 16, 2026

  Zhuzhoushizuisuanshangmaoyouxiangongsi, of China

  MNIENT 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. Additionally, the bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard.

  Unclassified

• Consumer Product Recall · July 16, 2026

  Shenzhen Dami Trading Co., Ltd., dba Delightmi, of China

  Oitnlaughter LED Finger Lights

  The recalled 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 · July 16, 2026

  Wuxi Leclaire Home Products Co., Ltd., of China

  Wade Logan Annyka 9-Drawer Fabric 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 · July 16, 2026

  TOMY International, Inc., of Oak Brook, Illinois

  Boon PIVOT Collapsible Toddler Tower Kitchen Step Stools

  The recalled toddler towers can tip over while in use, posing a risk of serious injury and death, due to tip over and fall hazards.

  Unclassified

• Drug Recall · July 16, 2026

  Ascend Laboratories, LLC

  Dabigatran Etexilate Capsules, 75 mg, 30-count (3x10) blister pack further packaged in a carton, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, INDIA, Distributed by: MAJOR PHARMACEUTICALS

  Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability

  Class III

• Consumer Product Recall · July 16, 2026

  Madewell Inc., of Wenzhou Zhongbang Smoking Set Manufacturing Co., Ltd., doing business as Jobon Official Store, of China

  Jobon butane torch lighters

  The lighters violate the mandatory safety 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. In addition, the lighters failed to meet the pre-market lighter submission requirement needed to demonstrate that the lighters feature child-resistant mechanisms and ensuring their safety and compliance with U.S. regulations.

  Unclassified

• Drug Recall · July 16, 2026

  Fresenius Kabi USA, LLC

  Xylocaine (lidocaine HCl Injection, USP), 1%, 200 mg per 20 mL (10 mg per mL), 25 Multiple-Dose Vials, 20 mL, Rx only, Sterile, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-485-27; NDC Vial:

  Presence of Particulate Matter: Hair was found in products

  Class II

• Drug Recall · July 16, 2026

  Ascend Laboratories, LLC

  Dabigatran Etexilate Capsules, 150 mg, 60-count (6x10) blister pack further packaged in a carton, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, INDIA, Distributed by: MAJOR PHARMACEUTICAL

  Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability

  Class III

• Drug Recall · July 16, 2026

  Fresenius Kabi USA, LLC

  Glycopyrrolate Injection, USP, 1 mg per 5 mL (0.2 mg per mL), 25 x 5 mL fill in a 6.5 mL vial, Rx only, Multiple Dose Vials, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-578-05; NDC Vial: 6

  Presence of Particulate Matter: Hair was found in product

  Class II

• Drug Recall · July 16, 2026

  Fresenius Kabi USA, LLC

  Xylocaine (lidocaine HCl Injection, USP), 1%, 500 mg per 50 mL (10 mg per mL), 25 Multiple-Dose Vials, 50 mL, Rx only, Sterile, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-485-57; NDC Vial:

  Presence of Particulate Matter: Hair was found in products

  Class II

• Consumer Product Recall · July 16, 2026

  Yiwushi Bihe Trading Co., Ltd., of China

  SDADI Kitchen Step Stools, models LT01 and LT05

  The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of serious injury and death due to tip over, fall and entrapment hazards.

  Unclassified

• Drug Recall · July 16, 2026

  Ascend Laboratories, LLC

  Dabigatran Etexilate Capsules, 75 mg, 60-count (6x10)blister pack further packaged in a carton, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, INDIA, Distributed by: MAJOR PHARMACEUTICALS,

  Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability

  Class III

• Consumer Product Recall · July 16, 2026

  Dongguan Shinneng Huizheng Network Technology Co., Ltd., dba Hurzein

  Noerishia 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 · July 16, 2026

  Panasonic Manufacturing (Xiamen) Co., Ltd, of Xiamen, Fujian, China

  Electric Toaster Ovens

  The power cord insulation can be insufficient due to a protective fiberglass sleeve not covering it adequately, posing a risk of shock and/or fire hazard.

  Unclassified

• Drug Recall · July 16, 2026

  Central Admixture Pharmacy Services Inc

  Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Compound Volume 416.8 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharm

  Incorrect Product Formulation

  Class III