Safety Recalls

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

Showing 801–850 of 17,395

• Medical Device Recall · July 10, 2026

  Medline Industries, LP

  Medline convenience kits labeled as: 1) MAJOR PROCEDURE, Medline Kit SKU CDS982040U; 2) OPERATIVE LAP P&S SURGICAL, Medline Kit SKU DYNJ89608; 3) LAPAROSCOPY, Medline Kit SKU DYNJ903479L; 4)

  Kits contain a potentially contaminated component which were recalled by the manufacturer

  Class II

• Medical Device Recall · July 10, 2026

  Medline Industries, LP

  Medline convenience kits labeled as: 1) OPEN HEART PACK, Medline Kit SKU CDS840393P; 2) OPEN HEART PACK, Medline Kit SKU CDS840393Q; 3) OPEN HEART PROCEDURE, Medline Kit SKU CDS980895W; 4) VA

  Kits contain a potentially contaminated component which were recalled by the manufacturer

  Class II

• Medical Device Recall · July 10, 2026

  GE Medical Systems Information Technologies Inc

  GE Healthcare Portrait Core Services SW V 1.2.0, REF 5700592. patient monitoring system

  A software vulnerability may allow unauthorized persons to gain privileged access to the device, which could result in loss of patient monitoring, missed patient alarms, and/or access to Protected Health Information (PHI).

  Class II

• Medical Device Recall · July 10, 2026

  AVID Medical, Inc.

  Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).

  The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.

  Class II

• Medical Device Recall · July 10, 2026

  Medline Industries, LP

  Medline convenience kits labeled as: 1) MAJOR GYN PACK, Medline Kit SKU DYNJG001030C; 2) GYN LITHOTOMY PACK, Medline Kit SKU DYNJT8166; 3) OPEN HEART PACK, Medline Kit SKU DYNJ47638B; 4) EAST

  Kits contain a potentially contaminated component which were recalled by the manufacturer

  Class II

• Medical Device Recall · July 10, 2026

  Medline Industries, LP

  Medline convenience kits labeled as: MAJOR HEAD AND NECK PPS, Medline Kit SKU DYNJ9425991S

  Kits contain a potentially contaminated component which were recalled by the manufacturer

  Class II

• Medical Device Recall · July 10, 2026

  Medline Industries, LP

  Medline convenience kits labeled as: 1) C-SECTION, Medline Kit SKU DYNJ904612L; 2) C-SECTION, Medline Kit SKU DYNJ911755; 3) AHR C-SECTION KIT, Medline Kit SKU DYNJ912014.

  Kits contain a potentially contaminated component which were recalled by the manufacturer

  Class II

• Medical Device Recall · July 10, 2026

  Medline Industries, LP

  Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M

  Kits contain a potentially contaminated component which were recalled by the manufacturer

  Class II

• Medical Device Recall · July 9, 2026

  AVID Medical, Inc.

  Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

  Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

  Class II

• Medical Device Recall · July 9, 2026

  AVID Medical, Inc.

  Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR W/STATLOCK Model/Catalog Number: SAMM064-27

  Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

  Class II

• Medical Device Recall · July 9, 2026

  Henry Schein Inc.

  Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm, Product Codes: 1) 949-3594, Mfr Product Code 1840; Lots 2529604, 2538147, 2608145 2) 949-3595, Mfr Product Code 1841; Lots 253

  Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.

  Class II

• Drug Recall · July 9, 2026

  CareFusion 213, LLC

  BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol), 60 x 1 mL applicators/carton, 0.03fl oz (1 mL) each, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subs

  Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator

  Class II

• Medical Device Recall · July 9, 2026

  AVID Medical, Inc.

  Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

  Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

  Class II

• Medical Device Recall · July 9, 2026

  Boston Scientific Corporation

  Boston Scientific ENROUTE Transcarotid Neuroprotection System, Material Number SR-200-NPS; Percutaneous catheter

  Potential for arterial sheath tip separation or partial tip separation during use.

  Class I

• Vehicle Recall · July 9, 2026

  Volvo Trucks North America

  2026 VOLVO VNL (4)

  A loose steering arm can result in a loss of vehicle steering control, increasing the risk of a crash.

  Unclassified

• Consumer Product Recall · July 9, 2026

  Best Buy Purchasing LLC, of Richfield, Minnesota

  Insignia Front Control Gas Ranges

  The recalled ranges' front-mounted knobs can be activated accidentally by humans or pets, posing a risk of serious injury from a fire hazard.

  Unclassified

• Consumer Product Recall · July 9, 2026

  shenzhenshiyuezhangwangluokejiyouxiangongsi (Shenzhen Yuezhang Network Technology Co., Ltd.), doing business as YUEZHANG, of China

  Moodooy 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 9, 2026

  Zhangzhoushi Jingqu Trading Co., Ltd., dba Wonder Stone Toys, of China

  WonderStone Infant 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 risk of serious injury or death due to a fall hazard.

  Unclassified

• Medical Device Recall · July 9, 2026

  AVID Medical, Inc.

  Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

  Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

  Class II

• Consumer Product Recall · July 9, 2026

  Conair LLC, of Stamford, Connecticut, dba Cuisinart

  Cuisinart Propel+ Four Burner 3-in-1 Gas Grill with pizza oven

  The tempered glass window in the pizza oven can shatter during use, posing a risk of serious injury from laceration hazard.

  Unclassified

• Consumer Product Recall · July 9, 2026

  iDecoz Inc. dba Flaunt, of Brooklyn, New York

  Flaunt MagSafe Battery Chargers

  The lithium-ion battery in the recalled power banks (chargers) can overheat and ignite, posing a risk of serious injury or death from fire and burn hazards.

  Unclassified

• Consumer Product Recall · July 9, 2026

  Jomani International Inc., of Monterey Park, California

  BBRKIN and MouTec Biometric Firearm Safes

  The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.

  Unclassified

• Consumer Product Recall · July 9, 2026

  Greenworks North America, LLC, dba Greenworks Tools, of Mooresville, North Carolina

  Kobalt 24V and 48V Trimmers, Blowers, Mowers, Chainsaws and Pruning Saws with USB-C Batteries

  Charging the lithium-ion batteries through the USB-C port, while the batteries are inserted in the yard power tools can cause the batteries to short-circuit, posing a risk of serious injury from fire hazard.

  Unclassified

• Medical Device Recall · July 9, 2026

  AVID Medical, Inc.

  Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

  Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

  Class II

• Medical Device Recall · July 9, 2026

  Boston Scientific Corporation

  Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus, Material Number SR-250-NPS; Percutaneous catheter

  Potential for arterial sheath tip separation or partial tip separation during use.

  Class I

• Medical Device Recall · July 9, 2026

  AVID Medical, Inc.

  Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

  Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

  Class II

• Medical Device Recall · July 9, 2026

  Henry Schein Inc.

  Structur 2 SC Temporary Resin Cartridge Refill 75Gm, Product Codes: 1) 114-3933, Mfr Product Code 1479; Lots 2536179, 2606429 2) 114-3934, Mfr Product Code 1480; Lot 2539064 3) 114-3935, Mfr Pro

  Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.

  Class II

• Medical Device Recall · July 9, 2026

  AVID Medical, Inc.

  Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

  Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

  Class II

• Food Recall · July 9, 2026

  Pack'n Fresh LLC

  "***Hondashi 0.25oz***" seasoning packed in silver plastic/metallic pouch, pouches packed in brown paperboard cartons (600 packets/carton), Carton label reads in part as "***Hondashi 0.25oz*600bags/ct

  Allergen missing from contains statement: fish

  Class II

• Medical Device Recall · July 8, 2026

  Tobii Dynavox Llc

  TD Navio Maxi Speech Generating Device Model/Catalog Number: 1000799

  Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an internal short circuit. This may cause localized heating and gas venting within the device enclosure.

  Class II

• Medical Device Recall · July 8, 2026

  Fort Defiance Industries, LLC

  Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131

  The Automated Field Steam Sterilizer's water recovery system 120V Amphenol connector may experience an intermittent loss of ground continuity, which could result in an unreliable fault current return path.

  Class II

• Medical Device Recall · July 8, 2026

  Medline Industries, LP

  Medline medical convenience kits, labeled as: 1) CRANIOTOMY PACK, Medline Kit SKU DYNJT6545; 2) ORTHO SPINE PACK, Medline Kit SKU DYNJ88056A; 3) ENT SINUS PACK, Medline Kit SKU DYNJ89001; 4)

  Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of endotoxin of the neurosponges.

  Class II

• Vehicle Recall · July 8, 2026

  KTM North America, Inc.

  2024 HUSQVARNA FE 350S

  Cracks or breaks in the rear brake caliper can reduce braking ability, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · July 8, 2026

  Medline Industries, LP

  Medline medical convenience kits, labeled as: 1) LAMINECTOMY PACK, Medline Kit SKU DYNJT6548; 2) ORTHO SPINE PACK, Medline Kit SKU DYNJ44504G; 3) NEURO SPINE PACK, Medline Kit SKU DYNJ45419F;

  Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of endotoxin of the neurosponges.

  Class II

• Food Recall · July 8, 2026

  Man Fon, Inc.

  Wonton Wrappers packed into clear flexible plastic bag and sold as 40 units (16oz bags)/case. Wonton Wrappers packed into "Wonton Noodles Net Wt. 5 LBS" plastic bags and sold as 10 units (4-lb bags)/

  No labeling. Undeclared wheat and colors: Yellow#5, Yellow#6.

  Class II

• Medical Device Recall · July 8, 2026

  Medline Industries, LP

  Medline medical convenience kits, labeled as: 1) NEURO CDS, Medline Kit SKU CDS985246J; 2) NEURO PACK, Medline Kit SKU DYNJ32770V; 3) NEURO BUNDLE-LF, Medline Kit SKU DYNJ40095D; 4) NEURO PAC

  Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of endotoxin of the neurosponges.

  Class II

• Vehicle Recall · July 8, 2026

  PACCAR Incorporated

  2026 PETERBILT 579, 2027 KENWORTH T680

  An incorrectly installed quick release valve that does not function properly can increase the risk of a crash.

  Unclassified

• Drug Recall · July 8, 2026

  Ascend Laboratories, LLC

  Amlodipine and Olmesartan Medoxomil Tablets, 10 mg/20 mg, 30 Tablets per bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC., Parsnippany, NJ 07

  Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications

  Class II

• Vehicle Recall · July 8, 2026

  Forest River, Inc.

  2027 FOREST RIVER WILDWOOD

  Referencing the incorrect GVWR may lead to unintentionally overloading the vehicle, increasing the risk of a crash.

  Unclassified

• Food Recall · July 8, 2026

  Green Jeeva LLC

  Organic Moringa Powder; 15kg/bag (bulk); Product code: GJ96

  Moringa Powder ingredient positive for salmonella

  Class I

• Food Recall · July 8, 2026

  Man Fon, Inc.

  Man Fon Inc. Won Ton Wrappers Extra Thin; Net Wt. 10 oz; UPC# 757168 977315, Keep Refrigerated, Can be Frozen. Sold in 48 units (10oz)/case.

  Undeclared colors: Yellow#5, and Yellow#6.

  Class II

• Medical Device Recall · July 8, 2026

  Tobii Dynavox Llc

  TD Navio Midi Speech Generating Device Model/Catalog Number: 1000798

  Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an internal short circuit. This may cause localized heating and gas venting within the device enclosure.

  Class II

• Medical Device Recall · July 8, 2026

  Medline Industries, LP

  Medline medical convenience kits, labeled as: 1) SINUS PACK-LF, Medline Kit SKU DYNJ0966146F; 2) ENT PACK, Medline Kit SKU DYNJ40154D; 3) ENT PACK, Medline Kit SKU DYNJ40154F; 4) ENT SCOPE PA

  Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of endotoxin of the neurosponges.

  Class II

• Medical Device Recall · July 7, 2026

  Olympus Corporation of the Americas

  Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual display unit designed for displaying graphical information in color.

  Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities.

  Class II

• Vehicle Recall · July 7, 2026

  Subaru of America, Inc.

  2023 SUBARU ASCENT, 2024 SUBARU ASCENT, 2025 SUBARU FORESTER, 2025 SUBARU ASCENT

  An incorrect GAWR label may lead to an overloaded vehicle, increasing the risk of a crash.

  Unclassified

• Vehicle Recall · July 7, 2026

  Tesla, Inc.

  2024 TESLA MODEL 3

  A noncompliant vehicle may have reduced occupant protections, increasing the risk of injury during a crash.

  Unclassified

• Medical Device Recall · July 7, 2026

  INTEGRATED MEDCRAFT LLC

  Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affected One-piece Guedel airway components: 1. Size 00, ISO 5.0, blue. Product Code: 1100050. 2. Size 000, IS

  Devices could potentially contain an occluded or partially occluded Guedel Airway tip.

  Class II

• Medical Device Recall · July 7, 2026

  INTEGRATED MEDCRAFT LLC

  FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12). REF Number: 1011-40002. Containing the affected One-piece Guedel airway components: 1. Size 00, ISO 5.0, blue. Product Code: 1100050.

  Devices could potentially contain an occluded or partially occluded Guedel Airway tip.

  Class II

• Medical Device Recall · July 6, 2026

  PI CARDIA LTD

  Pi-Cardia Inc. ShortCut REF: Z-A-20.003-US

  Transfemoral catheter, positing arm may detached due to weld issue.

  Class II

• Medical Device Recall · July 6, 2026

  Waldemar Link GmbH & Co. KG (Mfg Site)

  Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, Rotating Hinge Item Number 15-0027/16

  The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a prolonged or modified surgery as the plateau cannot be inserted and an alternative product would be needed. If the incorrect plateau were to be implanted, this is associated with increased risk of wear, which could result in a reduced standing time of the implant.

  Class II