Safety Recalls

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

Showing 601–650 of 17,395

• Drug Recall · July 24, 2026

  American Regent, Inc.

  niCARdipine Hydrochloride Injection, USP, 25 mg/10mL (2.5 mg/mL), packaged in a) 10 mL Single Dose Vial (NDC 72572-470-01) and b) 10x10 mL Single Dose Vials (NDC 72572-470-10), Rx Only, Mfd for: Civic

  Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

  Class II

• Drug Recall · July 24, 2026

  American Regent, Inc.

  Tralement (trace elements injection 4*, USP), packaged in a) 1mL Single Dose vials (NDC 0517-9305-01) and b) 5x1mL Single Dose vials (NDC 0517-9305-25), Rx only, AMERICAN REGENT, INC., SHIRLEY, NY 119

  Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

  Class II

• Medical Device Recall · July 24, 2026

  Biomerieux Inc

  VITEK 2 AST-N461 TEST KIT, GRAM NEGATIVE SUSCEPTIBILITY TESTING - AUTOMATED, Reference Number 424811

  The issue is related to card pouch damage associated with a portion of the lot which was produced on a specific card pouching device, in a specific timeframe, causing a potential risk of false resistant results. False resistant results may lead to the use of less effective antibiotic treatments or the association of multiple antibiotics having negative side effects, which could potentially impact patient s health.

  Class II

• Drug Recall · July 24, 2026

  American Regent, Inc.

  Papaverine HCl Injection, USP, 60 mg/2 mL (30 mg/mL), packaged in a) 2mL Single-Dose Vial (NDC 0517-4002-01), and b) 25x2mL Single-Dose Vials (NDC 0517-4002-25), Rx Only, AMERICAN REGENT, INC., SHIRLE

  Presence of Particulate Matter: Product contaminated with particulate matter identified as glass and/or paraformaldehyde

  Class I

• Drug Recall · July 24, 2026

  American Regent, Inc.

  ACETYLCYSTEINE SOLUTION, USP, 20% (200 mg/mL), packaged in a) 4 mL Vial NOT FOR INJECTION (NDC 0517-7604-01), and b) 25x4 mL Vials NOT FOR INJECTION (NDC 0517-7604-25), Rx only, AMERICAN REGENT, INC.,

  Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

  Class II

• Medical Device Recall · July 24, 2026

  Spectral Instruments Inc

  Lago X

  Momentary absence of On-Screen "X-Ray On" banner during run readiness check.

  Class II

• Medical Device Recall · July 24, 2026

  Spectral Instruments Inc

  Ami HTX

  Momentary absence of On-Screen "X-Ray On" banner during run readiness check.

  Class II

• 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

• Drug Recall · July 24, 2026

  Baxter Healthcare Corporation

  Cefazolin in Dextrose, Injection, USP, 2g / 100mL (20mg / mL) Single-Dose Infusion Bag in 100mL GALAXY Plastic Container, Frozen Premix, Sterile, Rx only, Manufactured by Baxter Healthcare Corporation

  Presence of Particulate Matter

  Class I

• Vehicle Recall · July 23, 2026

  BMW of North America, LLC

  2023 BMW S 1000 RR, 2024 BMW S 1000 RR, 2025 BMW S 1000 RR

  An engine stall or failure of electrical systems such as the instrument display or ABS, increases the risk of a crash.

  Unclassified

• Medical Device Recall · July 23, 2026

  Medical Action Industries, Inc. 306

  Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451; Blood Culture Kit 20/Cs, REF: 81834B; Blood Culture Collection Kit, REF: 81834C. All containing BD ChloraPrep Clear - 1 mL Applicators

  Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the component's sterile barrier and if used may lead to localized skin or soft tissue infection.

  Class II

• 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

• Medical Device Recall · July 23, 2026

  Medos International Sarl

  Velys Enabling Tech Robotic-Assist Station REF: 451611001

  Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning.

  Class II

• Medical Device Recall · July 23, 2026

  Medical Action Industries, Inc. 306

  Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules

  Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

  Class I

• 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

  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

  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

• Medical Device Recall · July 23, 2026

  Medical Action Industries, Inc. 306

  Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules

  Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

  Class I

• 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

• 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

  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

• 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

• 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

• 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

• Medical Device Recall · July 23, 2026

  Medline Industries, LP

  Medline Convenience Kit: OPEN HEART A PACK, Product Number DYNJ43008N

  The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach. Sterility of the product cannot be assured. If a compromised pouch seal is not identified prior to use and the cannula is used, there is a potential risk of infection or other complications associated with the use of a non-sterile device, including hemolysis, foreign body reaction, thromboembolism, and/or organ dysfunction.

  Class II

• Food Recall · July 22, 2026

  Lidl US TRADING

  ERIDANOUS GREEK STYLE Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling. Product is packed onto a plastic carton tray with outer paper sleeve, 330 g (weight), UPC: 4056489125839.

  The firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coconut).

  Class II

• Medical Device Recall · July 22, 2026

  AVID Medical, Inc.

  Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02

  Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.

  Class II

• Food Recall · July 22, 2026

  Coast Citrus Distributors

  Jalapeno Pepper packaged in bulk generic Coast Tropical cardboard packaging. Packaged in assorted bulk package sizes (10lbs, 40lbs, 35lbs, 20lbs, 38lbs 1 1/9 Bushel) ; Product of MX; Coast Tropical TX

  Potential Salmonella Javiana contamination

  Class I

• Vehicle Recall · July 22, 2026

  Volkswagen Group of America, Inc.

  2024 VOLKSWAGEN ATLAS, 2024 VOLKSWAGEN ATLAS CROSS SPORT, 2025 VOLKSWAGEN ATLAS, 2025 VOLKSWAGEN ATLAS CROSS SPORT

  A rearview camera that fails to display an image can reduce the driver’s view behind the vehicle, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · July 22, 2026

  AVID Medical, Inc.

  Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-01

  Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.

  Class II

• Medical Device Recall · July 22, 2026

  Boston Scientific Corporation

  Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1) DVI to HDMI Cable, (1) DisplayPort Cable REF: M0067933000, M006793300H0, M006

  A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path. As a result, the power adaptor may fail electrical safety testing during installation.

  Class II

• Medical Device Recall · July 22, 2026

  AVID Medical, Inc.

  Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02.

  Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides.

  Class I

• Food Recall · July 22, 2026

  Lidl US TRADING

  ERIDANOUS GREEK STYLE Shortbread Cookies with apricot filling and cocoa topping with coconut sprinkles. Product is packed onto a plastic carton tray with outer paper sleeve, 330 g (weight), UPC: 40564

  The firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coconut).

  Class II

• Medical Device Recall · July 22, 2026

  FUJIFILM Healthcare Americas Corporation

  FUJIFILM Synapse PACS software v7.4.310; radiological image processing system

  Software issue may cause the ruler measurement to be inaccurate.

  Class II

• 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 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

• 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

• Medical Device Recall · July 22, 2026

  Merge Healthcare, Inc.

  Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation

  Software issue may cause measurements to be displayed inaccurately.

  Class II

• Vehicle Recall · July 21, 2026

  Ford Motor Company

  2025 FORD EXPLORER, 2025 LINCOLN AVIATOR

  Unexpected movement of the driver’s seat back may trap a second-row occupant, increasing the risk of injury.

  Unclassified

• Medical Device Recall · July 20, 2026

  Medline Industries, LP

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE KIT 2 W/CONNECT DYNDH1487A

  Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

  Class II

• Medical Device Recall · July 20, 2026

  SDI Limited

  Dentsply Sirona Capsule Mixer Model No. 5546068

  Potential for electrical discharge from unit when unplugged.

  Class II

• Vehicle Recall · July 20, 2026

  Blue Bird Body Company

  2023 BLUE BIRD VISION SCHOOL BUS, 2024 BLUE BIRD VISION SCHOOL BUS, 2026 BLUE BIRD VISION SCHOOL BUS

  A brake fluid leak in the presence of an ignition source such as hot engine or exhaust components can increase the risk of a fire. Additionally, a brake fluid leak can extend the distance required to stop, increasing the risk of a crash.

  Unclassified

• Vehicle Recall · July 20, 2026

  Ford Motor Company

  2023 FORD BRONCO, 2024 FORD BRONCO

  A short circuit in the engine compartment can create heat or spark, increasing the risk of a fire.

  Unclassified

• Medical Device Recall · July 20, 2026

  Medline Industries, LP

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE PINK PERIPHERAL DYNDV1875 BOTTOM DRAWER ACC010972 DRAWER #4 ACC010479A DRAWER 2 ACC

  Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

  Class II

• Medical Device Recall · July 20, 2026

  Medline Industries, LP

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ADULT BLOOD CULTURE KIT DYNDH1444D BLOOD CULTR KT DIVRSN DEVICE DYNDH1866 BLOOD CULTURE KIT DYNDH1462B DYN

  Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

  Class II

• Medical Device Recall · July 20, 2026

  Medline Industries, LP

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators LABOR CDS CDS981762B VAG DELIVERY ADMISSION BAG DYKA1054F

  Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

  Class II

• Medical Device Recall · July 20, 2026

  Paragonix Technologies Inc.

  Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF# PRGNX-8008-001

  Due to a firmware defect, the portable organ transfer device datalogger may lose its configuration, resulting in a blank screen and loss of displayed preservation parameters.

  Class II

• Medical Device Recall · July 20, 2026

  Medline Industries, LP

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PATIENT ADMIN KIT DYKA1384B DYKA1384C WELCOME KIT DYKS1206D

  Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

  Class II

• Medical Device Recall · July 20, 2026

  Medline Industries, LP

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ORTHO ASPIRATION KIT DYKM1636A

  Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

  Class II

• Medical Device Recall · July 20, 2026

  Midmark Corporation

  Midmark IQecg Digital ECG, Model/Catalog Number: 4-000-0061, 4-000-0062 Software Version: Midmark IQecg Plugin versions starting with v10 and prior to v10.1.0.18.

  A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.

  Class II