Safety Recalls

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

Showing 151–200 of 17,395

• Medical Device Recall · August 21, 2026

  Philips North America Llc

  Ingenia 1.5T, Ingenia 1.5T CX and Ingenia 1.5T S; Model Numbers (REF): 1. 781315(1.5T), 2. 781341(1.5T), 3. 781396(1.5T), 4. 782101(1.5T), 5. 782115(1.5T), 6. 782140(1.5T), 7. 781261(1.5T CX), 8. 781

  A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.

  Class II

• Drug Recall · August 21, 2026

  VITRUVIAS THERAPEUTICS INC

  Thyroid Tablets, USP, 1/2 Grain (30 mg), Each tablet contains: levothyroxine (T4) 19 mcg, liothyronine (T3) 4.5 mcg, 100 Tablets, Rx only, Distributed by: Vitruvias Therapeutics, Auburn, AL 36830, Pro

  Superpotent Drug

  Class I

• Medical Device Recall · August 21, 2026

  Midmark Corporation

  Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal), and oxygen saturation (SpO2) for adult and pediatric patients

  A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

  Class II

• Drug Recall · August 21, 2026

  Golden State Medical Supply Inc.

  Prasugrel HCI, Tablets, USP, 10mg, 30-count bottle, Rx only, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA, NDC: 51407-445-30.

  Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution

  Class II

• Medical Device Recall · August 21, 2026

  Midmark Corporation

  Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal), and oxygen saturation (SpO2) for adult and pediatric patients

  A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

  Class II

• Medical Device Recall · August 21, 2026

  Philips North America Llc

  MR 7700 and Upgrade to MR 7700; Model Number (REF): 1. 782120, 2. 782153, 3. 782130 (Upgrade);

  A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.

  Class II

• Medical Device Recall · August 21, 2026

  Philips North America Llc

  MR 5300 Model Number (REF): 1. 782110, 2. 782152;

  A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.

  Class II

• Medical Device Recall · August 21, 2026

  Philips North America Llc

  Name (Model Number): 1. Intera 1.5T (781195), 2. Intera 1.5T (781295), 3. Intera 1.5T Achieva IT Nova (781175), 4. Intera 1.5T Achieva Nova (781172), 5. Intera 1.5T Achieva Nova-Dual (781173), 6. Inte

  A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.

  Class II

• Medical Device Recall · August 21, 2026

  Philips North America Llc

  Ingenia Ambition S and Ingenia Ambition X; Model Numbers (REF): 1. 781359 (S), 2. 782108 (S), 3. 782139 (S), 4. 781356 (X), 5. 782109 (X), 6. 782138 (X);

  A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.

  Class II

• Medical Device Recall · August 21, 2026

  Philips North America Llc

  Achieva XR; Model Numbers (REF): 1. 781153, 2. 781253;

  A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.

  Class II

• Vehicle Recall · August 21, 2026

  Kia America, Inc.

  2025 KIA EV9

  A child in the front seat may be at a greater risk of injury if the air bag deploys during a crash.

  Unclassified

• Vehicle Recall · August 21, 2026

  PACCAR Incorporated

  2027 KENWORTH T680

  A short circuit increases the risk of a fire.

  Unclassified

• Medical Device Recall · August 21, 2026

  Philips North America Llc

  Achieva 3.0T; Model Numbers (REF): 1. 781177, 2. 781277, 3. 781278, 4. 781344, 5. 781345;

  A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.

  Class II

• Medical Device Recall · August 21, 2026

  Midmark Corporation

  Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal), and oxygen saturation (SpO2) for adult and pediatric patients

  A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

  Class II

• Medical Device Recall · August 21, 2026

  Philips North America Llc

  SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T, SmartPath to dStream for XR and 3.0T, SmartPath to Ingenia Elition X; Model Numbers (REF): 1. 781260 (1.5T), 2. 782112 (1.5T), 3. 782146

  A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.

  Class II

• Medical Device Recall · August 21, 2026

  Philips North America Llc

  Ingenia Elition S and Ingenia Elition X; Model Numbers (REF): 1. 781357(S), 2. 782106(S), 3. 782137(S), 4. 781358(X), 5. 782107(X), 6. 782119(X), 7. 782136(X), 8. 782158(X);

  A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.

  Class II

• Medical Device Recall · August 21, 2026

  Philips North America Llc

  Evolution upgrade 1.5T and Evolution upgrade 3.0T; Model Numbers (REF): 1. 782116 (1.5T), 2. 782148 (1.5T), 3. 782117 (3.0T), 4. 782143 (3.0T);

  A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.

  Class II

• Medical Device Recall · August 21, 2026

  Midmark Corporation

  Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal), and oxygen saturation (SpO2) for adult and pediatric patients

  A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

  Class II

• Medical Device Recall · August 21, 2026

  Philips North America Llc

  Ingenia 3.0T and Ingenia 3.0T CX; Model Numbers (REF): 1. 781342(3.0T), 2. 781377(3.0T), 3. 782103(3.0T), 4. 781271(3.0T CX), 5. 782105(3.0T CX);

  A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.

  Class II

• Drug Recall · August 21, 2026

  Lexia LLC

  Broadway Joe's Pain Cream, (Histamine Dihydrochloride 0.025%), 1500mg CBD Isolate, 1000mg Hempseed oil, 2 oz-jar, Produced for Broadway Joe's, Franklin, TN, 37067, NDC 83088-8120-5, UPC 8 50041 64003

  CGMP Deviations: Potential contamination of raw material

  Class II

• Drug Recall · August 21, 2026

  Lexia LLC

  Broadway Joe's Pain Cream, 3000 gm CBD, (Histamine Dihydrochloride 0.025%) (CDB Isolate 3000mg, HempSeed Oil 2000mg),4 oz-jar, Produced for Broadway Joe's, Franklin, TN, 37067, NDC 83088-8120-6; UPC 8

  CGMP Deviations: Potential contamination of raw material

  Class II

• Drug Recall · August 20, 2026

  Sterling Pharmaceutical Services LLC

  TRP The Relief Products* Gentle Eyes Lubricant Eye Drops, Carboxymethylcellulose sodium 0.5%, Sterile Eye Drops, 0.5 FL OZ (15 mL) bottles, Manufactured exclusively for TRP Company, Inc. 1575 Delucci

  Lack of Assurance of Sterility

  Class II

• Drug Recall · August 20, 2026

  Sterling Pharmaceutical Services LLC

  AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Drops, Sterile, 0.5 FL OZ (15 mL) EACH, 1.0 FL OZ (30 mL) TOTAL, 2 count Twin Pack, Distributed by: AVKARE, Pulaski, TN, 38

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · August 20, 2026

  Wilson-Cook Medical Inc.

  Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Model/Catalog Number: HEMO-7, HEMO-10, HEMO-7-EU, HEMO-10-EU Software Version: N/A Product Description: Hemost

  Due to issue with endoscope adherence and inability to spray powder. Firm will provide an updated Instruction for Use (IFU).

  Class II

• Vehicle Recall · August 20, 2026

  Lucid USA, Inc.

  2023 LUCID AIR, 2024 LUCID AIR, 2025 LUCID AIR

  An overheated circuit increases the risk of a fire. A loss of the center brake light or front lights can also decrease visibility, increasing the risk of a crash.

  Unclassified

• Drug Recall · August 20, 2026

  Sterling Pharmaceutical Services LLC

  AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Drops, Sterile, 0.5 FL OZ (15 mL) bottle, Distributed by: AVKARE, Pulaski, TN, 38478, NDC 50268-068-15

  Lack of Assurance of Sterility

  Class II

• Consumer Product Recall · August 20, 2026

  Dreams Bedding Technology PTE. Ltd., of Singapore

  Koorlian Mattresses

  The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire.

  Unclassified

• Drug Recall · August 20, 2026

  Sterling Pharmaceutical Services LLC

  Reliable -1 Laboratories, Sodium Chloride Hypertonicity Ophthalmic Solution, 5%, Sterile, 0.5 FL OZ (15 mL) bottles, Distributed by: Reliable-1 Laboratories LLC, Valley Stream, NY, 11580, NDC 69618-07

  Lack of Assurance of Sterility

  Class II

• Drug Recall · August 20, 2026

  Sterling Pharmaceutical Services LLC

  Walgreens Lubricant Eye Drops, 0.5 FL OZ (15 mL) 1.0 FL OZ (30 mL) TOTAL, 2 count Twin Pack, Distributed by Walgreens Co., 200 Wilmot Road, Deerfield, IL 60015, NDC 0363-8833-15.

  Lack of Assurance of Sterility

  Class II

• Vehicle Recall · August 20, 2026

  General Motors, LLC

  2024 BUICK ENCORE GX, 2024 BUICK ENVISTA, 2024 CHEVROLET TRAILBLAZER, 2025 BUICK ENCORE GX, 2025 BUICK ENVISTA, 2025 CHEVROLET TRAILBLAZER, 2025 CHEVROLET TRAX

  A rearview image that does not display correctly reduces the driver's view behind the vehicle, increasing the risk of a crash.

  Unclassified

• Drug Recall · August 20, 2026

  Sterling Pharmaceutical Services LLC

  Walgreens Lubricant Eye Drops, Carboxymethylcellulose sodium 0.5%, Lubricant Eye Drops, Sterile, 0.5 OZ (15 mL) bottles, Distributed by Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-8833

  Lack of Assurance of Sterility

  Class II

• Drug Recall · August 20, 2026

  Sterling Pharmaceutical Services LLC

  Reliable-1 Laboratories Lubricating Tears, Sterile, 0.5 FL OZ (15 mL) bottles, Distributed by: Reliable-1 Laboratories LLC, Valley Stream, NY, 11580, www.reliable1labs.com, NDC 69618-076-55.

  Lack of Assurance of Sterility

  Class II

• Vehicle Recall · August 20, 2026

  Marathon Industries Inc.

  2025 FORD F-650 SD

  A liftgate that falls unexpectedly increases the risk of injury.

  Unclassified

• Medical Device Recall · August 20, 2026

  ICU Medical, Inc.

  CADD Yellow Medication Cassette Reservoir with NRFit connector US Product Codes: 21-7600-24, 21-7609-24 OUS Product Codes: 21-7609-24 21-7600-24 21-7600-24 21-7600-24 21-7609-24 21-7609-24

  Reservoirs may exhibit medication leakage at the joint between luer connector and tubing. Issue could result in delay or interruption of therapy, under delivery of medication, exposure to infectious or toxic agents, or air embolus.

  Class II

• Consumer Product Recall · August 20, 2026

  CCM Hockey U.S., Inc., of Maple Grove, Illinois

  FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories

  The recalled hockey visors and replacement visor accessories can crack upon impact, posing a risk of injury due to laceration or impact hazards.

  Unclassified

• Consumer Product Recall · August 20, 2026

  Shenzhen Jinhe Trade Co., Ltd., dba Mystic ZO, of China

  JINHEZO Mini Waterproof LED Tea Lights

  The LED Tea Lights 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 20, 2026

  KTM North America Inc., of Amherst, Ohio

  GASGAS and Husqvarna Off-Road Motorcycles

  The rear brake caliper can crack or break, reducing the brake system's effectiveness, posing a risk of serious injury or death due to crash hazard.

  Unclassified

• Consumer Product Recall · August 20, 2026

  Modine Manufacturing Company, of Racine, Wisconsin

  Ventilation Fans in ClassMate® DX Cooling and Air Source Heat Pumps and SchoolMate® Water/Ground Source Heat Pumps

  The ventilation fan motor in the heat pumps can short circuit if water gets on the circuit board, causing the units to overheat and posing a fire hazard.

  Unclassified

• Medical Device Recall · August 20, 2026

  DeRoyal Industries Inc

  REF: 81-030415 Myocardial Probe Non-Pyrogenic , 400 Series

  Myocardial temperature probes contain an incorrect needle. Specifically, an 18mm needle was included instead of a 15mm needle.

  Class II

• Consumer Product Recall · August 20, 2026

  Goal Zero, of Draper, Utah

  Goal Zero YETI 3000X Portable Power Stations

  The recalled power station's circuit board can overheat, posing a risk of serious injury from fire and burn hazards.

  Unclassified

• Consumer Product Recall · August 20, 2026

  Guangzhou Ao Lian Ya Wang Luo Ke Ji You Xian Gong Si, dba Workbless, of China

  Workbless Electric Pressure Washers

  The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing serious risks of injury or death from shock and electrocution hazards.

  Unclassified

• Drug Recall · August 20, 2026

  Sterling Pharmaceutical Services LLC

  Lubricant Eye Drops-Cameron Pharmaceuticals, Carboxymethylcellulose Sodium 0.5%, Eye Lubricant, 0.5 FL OZ (15 mL) bottles, Distributed by Cameron Pharmaceuticals, LLC, Louisville, KY, 40245, NDC 42494

  Lack of Assurance of Sterility

  Class II

• Drug Recall · August 20, 2026

  Sterling Pharmaceutical Services LLC

  Major LubriFresh P.M. Nighttime Ointment, Net wt. 0.125 oz. (3.5 g) tubes, Distributed by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, NDC 0904-6488-38

  Lack of Assurance of Sterility

  Class II

• Drug Recall · August 19, 2026

  American Health Packaging

  Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC#: 60687-481-21, (Individual Dose NDC: 60687-481-

  Labeling: Label Mix-up

  Class III

• Medical Device Recall · August 19, 2026

  Olympus Corporation of the Americas

  Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector. Model/Catalog Number: CD-B622LA.

  Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.

  Class II

• Medical Device Recall · August 19, 2026

  Stryker Sustainability Solutions

  REF:B11LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 11X100MM

  Reusable access port system may crack or seperate during use.

  Class II

• Medical Device Recall · August 19, 2026

  Olympus Corporation of the Americas

  Olympus BiCOAG Hemostasis Probe 10Fr Fixed Pin Connector. Model/Catalog Number: CD-B612LA.

  Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.

  Class II

• Medical Device Recall · August 19, 2026

  BD SWITZERLAND SARL

  BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter, Back Check Valve, 3 SmartSite Y-sites 10015861A 10885403232626 50885403232624 BD Ala

  Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.

  Class I

• Food Recall · August 19, 2026

  United Sugar Producers and Refiners

  Powdered Sugar, Packaged in the following configurations: 1. United 6X, Net Wt. 50 lbs. (22.68kg), Item Number 810087. UPC 7 85921-07090 4. Distributed by: United Sugar Producers & Refiners, Min

  Potential Wheat Kernel contamination.

  Class II

• Medical Device Recall · August 19, 2026

  SEASPINE ORTHOPEDICS CORPORATION

  SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head, Attached Gimbal, 12mm REF: MD1-300010-12

  The proximal thread depth of the spinal device is out of design specification.

  Class II