Safety Recalls

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

Showing 701–750 of 17,395

• 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

  Fresenius Kabi USA, LLC

  Lidocaine HCl Injection, USP, 2%, 100 mg per 5 mL (20 mg per mL), 25 Single Dose Vials, 5 mL per vial, Rx only, Sterile, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-208-05; NDC Vial: 63323

  Presence of Particulate Matter: Hair was found in products

  Class II

• 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

  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

• 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

• Consumer Product Recall · July 16, 2026

  Target, of Minneapolis, Minnesota

  Cat & Jack Children's Sandals

  The sandals' decorative pearls can fall off, posing a risk of serious injury or death from a choking hazard.

  Unclassified

• 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

  J. Crew Group, LLC of New York, New York

  Madewell Double V-Neck Pullover and V-Neck Cardigan Sweaters

  The recalled sweaters violate the mandatory standard for clothing textiles, posing a risk of serious burn injuries or death.

  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

  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

  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

  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

• Medical Device Recall · July 16, 2026

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232, 722233, 722234, 722235, and 722236, with Software Version Numbers: R3.0 and R3.1; Interventional fluoroscopic x-ray system

  Two software related issues: 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

• 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

• 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

  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

• Food Recall · July 16, 2026

  CHEER PACK

  Flexible food pouch (3-layer foil, spouted, #CP6088), manufactured for packaging Pumpkin Tree Peter Rabbit Organics Banana & Strawberry, 4 oz food puree, UPC 815367010780.

  Flexible food pouch may release thin plastic strips into food.

  Class II

• 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

• 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

• 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

• Medical Device Recall · July 15, 2026

  F & A Foundation

  Reign Medical Clench Staple System (Compression), Description/REF: 9mm x 7mm/152-30907; 11mm x 10mm/152-31110; 15mm x 12mm/152-31512; 18mm x 18mm/152-31818; 20mm x 20mm/152-32020; 9mm x 7mm/15

  Bone fixation staple requires a new 510(k); the performance characteristics of this device have not been adequately established.

  Class II

• Vehicle Recall · July 15, 2026

  Nissan North America, Inc.

  2023 INFINITI QX80, 2023 NISSAN ARMADA, 2024 INFINITI QX80, 2024 NISSAN ARMADA, 2025 INFINITI QX80, 2025 NISSAN ARMADA, 2027 INFINITI QX80

  An overloaded vehicle can increase the risk of a crash.

  Unclassified

• Medical Device Recall · July 15, 2026

  Beckman Coulter Inc.

  Beckman Coulter DxC 500 AU Clinical Analyzer Modules using software version 1.5 or lower: 1) AU w/out ISE, Part Number C63519; 2) AU w/ISE, Part Number C63520; DxC 500 AU Clinical Chemistry Analy

  a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously modified by the user, upon import of a new Parameter Package version. As a result, usercustomized calculated test rules revert silently to their default expressions, potentially generating erroneous patient test results without an explicit error notification. The issue affects instruments running software version 1.5 or lower and only occurs when a new Parameter Package is imported to a system that already has an existing Parameter Package onboard; new installations are not affected.

  Class II

• Food Recall · July 15, 2026

  Prospector Popcorn, LLC

  Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.

  Inaccurately declared nutrients including Potassium (overstated), Calcium (overstated), and Iron (understated).

  Class III

• Food Recall · July 15, 2026

  Prospector Popcorn, LLC

  Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3.5oz

  Inaccurately declared nutrients including Potassium (overstated) and Calcium (overstated).

  Class III

• Medical Device Recall · July 15, 2026

  Beckman Coulter Inc.

  Beckman Coulter DxC 500i Clinical Analyzer Modules using software version 1.5 or lower: 1) DxC 500 AU Module w/ISE, DxC 500i, Part Number C63522; 2) DxC 500 AU Module, DxC 500i, Part Number C6352

  a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously modified by the user, upon import of a new Parameter Package version. As a result, usercustomized calculated test rules revert silently to their default expressions, potentially generating erroneous patient test results without an explicit error notification. The issue affects instruments running software version 1.5 or lower and only occurs when a new Parameter Package is imported to a system that already has an existing Parameter Package onboard; new installations are not affected.

  Class II

• Food Recall · July 15, 2026

  Prospector Popcorn, LLC

  Prospector Popcorn Belgian Chocolate Toffee Gourmet Popcorn 3.5oz

  Inaccurately declared nutrients including Iron (understated), and Vitamin D (overstated).

  Class III

• Drug Recall · July 15, 2026

  Asclemed USA Inc.

  Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use Only, Rx Only, Distributed by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC: 76420-760-01.

  Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan

  Class III

• Medical Device Recall · July 15, 2026

  BMC Medical Co., Ltd.

  BMC/REACTHEALTH Luna G3 APAP REF LG 3600

  Retroactive reporting for 2024 rework conducted at the 3B/React Health warehouse

  Class I

• Food Recall · July 15, 2026

  Prospector Popcorn, LLC

  Prospector Popcorn Chocolate Mocha Gourmet Popcorn 1.5 oz.

  Inaccurately declared nutrients including Carbohydrates (understated) and Cholesterol (understated).

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Optic Glow (naphazoline hydrochloride 0.03%, povidone 0.5%, propylene glycol 0.2%), Sterile, 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127,

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) NEWNAN SMR PACK, Catalog Number: SEN21SPPMB

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Medical Device Recall · July 14, 2026

  Fresenius Medical Care Renal Therapies Group, LLC

  NaturaLyte, Liquid Acid Concentrate for Bicarbonate Hemodialysis: Product Numbers: 08-1251-1, 08-2251-0, 08-2301-3, 08-3251-9, 08-3301-2, 13-2201-5, 13-2251-0, 13-3251-9; Liquid Acid Concentrate for

  Complaints of blue-green discoloration in product

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Dry Aid (povidone 0.68%, propylene glycol 0.3%), Sterile, TWIN PACK 0.34 FL OZ (10 mL) each, Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, U

  Lack of Assurance of Sterility

  Class II

• Vehicle Recall · July 14, 2026

  Ford Motor Company

  2023 FORD EXPLORER, 2023 LINCOLN AVIATOR, 2024 FORD EXPLORER, 2024 LINCOLN AVIATOR, 2025 FORD EXPLORER, 2025 LINCOLN AVIATOR

  A seat that moves unexpectedly may not properly restrain an occupant during a crash, increasing the risk of injury.

  Unclassified

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Cool Relief (naphazoline hydrochloride 0.012%, polysorbate 80 0.2%), Sterile, 0.4 FL OZ (13 mL) each, Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in V

  Lack of Assurance of Sterility

  Class II

• Vehicle Recall · July 14, 2026

  Hyundai Motor America

  2024 HYUNDAI KONA, 2024 HYUNDAI KONA ELECTRIC, 2025 HYUNDAI KONA, 2025 HYUNDAI KONA ELECTRIC

  A seat belt buckle that fails to properly restrain an occupant in a crash increases the risk of injury.

  Unclassified

• Medical Device Recall · July 14, 2026

  AVID Medical, Inc.

  Halyard IV Start Kit Non-Sterile REF: KRIV26-02

  Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal area.

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) BASIC PACK , Catalog Number: SBA73BPGCA; 2) SPINE PACK , Catalog Number: SNE11SPHKC; 3) SPINE PACK , Ca

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops ALL-IN-ONE (hypromellose 0.2%, tetrahydrozoline HCL 0.05%, zinc sulfate 0.25%), Sterile 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · July 14, 2026

  AVID Medical, Inc.

  Halyard IV START KIT NON-STERILE REF: KRIV26-02

  Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides

  Class I

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC27; 2) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC28; 3) CHI STD NEURO CRANI OPT 2 , Catal

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) SEPTO RHINO PACK , Catalog Number: SEN73NSKCF; 2) PACK NEURO MINOR CRANIOTOMY , Catalog Number: SNE30CNOHE; 3) NEURO MAJOR 2 PACK , Catal

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0.03%, polysorbate 90, 0.2%), Sterile 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietn

  Lack of Assurance of Sterility

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Dry Aid (povidone 0.68%, propylene glycol 0.3%), Sterile, 0.34 FL OZ (10 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310742011135

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT , Catalog Number: 21-4720B; 2) TRAY FAT GRAFT ADD , Catalog Number: 21-4720C; 3) KIT,BOSC MICROLARYNGOSCOPY , Catalog N

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Medical Device Recall · July 14, 2026

  Boston Scientific Corporation

  OverStitch Suture Cinch, 1pk. Endoscopic tissue approximation device.

  Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.

  Class II

• Medical Device Recall · July 14, 2026

  Hollister Ulc

  Onli 17cm Hydrophilic Urethral Intermittent Catheter, labeled as: 1) 82081 Ch08-17 Onli Hydrophilic Urethral Intermittent Catheter, SKU/REF 82081; 2) 82101 Ch10-17 Onli Hydrophilic Urethral Inter

  Hollister has identified that select lots of the catheters identified in the above table may exhibit a protrusion caused by a manufacturing defect which might lead to genitourinary trauma or bleeding.

  Class II