Safety Recalls

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

Showing 951–1,000 of 17,395

• Medical Device Recall · June 25, 2026

  Pride Mobility Products Corp.

  Brand Name: Quantum Rehab Product Name: Quantum 1450 Model/Catalog Number: Quantum 1450 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Comp

  If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

  Class II

• Food Recall · June 25, 2026

  Fresh & Ready Foods LLC

  Fresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10303, Net wt. 5.9oz. Product is refrigerated. UPC 1 00000 01030 3. Manufactured by LPK1 Renton, WA. Product was not sold at retail stores a

  Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.

  Class I

• Medical Device Recall · June 25, 2026

  Pride Mobility Products Corp.

  Brand Name: Quantum rehab Product Name: Q6 Edge 2.0 Model/Catalog Number: Q6 Edge 2.0 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Compon

  If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

  Class II

• Medical Device Recall · June 25, 2026

  C.R. Bard Inc

  Products that contain the Pericare Wipes: SureStep Intermittent Catheter Tray REF: INTP16 INTS14 INTS14C INTS16 INTS16C PEDINTS06 PEDINTS08 PEDINTS10 UDI code: 00801741183300¿ 10801741183307 00801741

  Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

  Class II

• Drug Recall · June 25, 2026

  Bell Pharmaceuticals, Inc

  LEADER, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), a) Kit -1 RUBBER BULB SYRINGE, 0.5 FL OZ DROPS, (NDC 70000-0689-1); b) 1 bottle (NDC 70000-0688-1), DIST. BY CARDINAL HEALTH, DUBLIN, OH 43017.

  SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

  Class II

• Consumer Product Recall · June 25, 2026

  Spector & Co., of Saint Laurent, of Quebec, Canada

  Super Off-Road 12,000 mAh Solar Wireless Power Banks

  The solar power bank's lithium-ion battery can swell and overheat, posing a burn hazard to consumers.

  Unclassified

• Medical Device Recall · June 25, 2026

  Pride Mobility Products Corp.

  Brand Name: Quantum Rehab Product Name: 4Front Model/Catalog Number: 4Front Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Contr

  If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

  Class II

• Medical Device Recall · June 25, 2026

  Pride Mobility Products Corp.

  Brand Name: Quantum Rehab Product Name: Q6 Edge 2.0 (ilevel) Model/Catalog Number: Q6 Edge 2.0 (ilevel) Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI)

  If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

  Class II

• Drug Recall · June 25, 2026

  Bell Pharmaceuticals, Inc

  QC Quality Choice, Carbamide Peroxide, 6.5%, 0.5 FL. OZ. (15 mL) a) Washer Bulb included (NDC 63868-026-15); b) 1 bottle (NDC 63868-027-16), Distributed by C.D.M.A., Inc., 43157 W. Nine Mile, Novi, MI

  SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

  Class II

• Consumer Product Recall · June 25, 2026

  Kith Retail Inc. of Brooklyn, New York

  Kids Kithmas Plaid Lounge Sets

  The recalled children's loungewear sets violate the mandatory flammability standards for children's sleepwear, posing a risk of serious burn injuries.

  Unclassified

• Consumer Product Recall · June 25, 2026

  Shield Line LLC, of Branchburg, New Jersey

  MedPride Baby Oil

  The baby oil contains low-viscosity hydrocarbons, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The baby oil's packaging is not child-resistant, posing a risk of serious injury or illness 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 · June 25, 2026

  Yongkang Ruihe Metal Products Co. Ltd., of China

  XW-A17 Electric Youth All-Terrain Vehicles (ATVs)

  The recalled youth ATVs violate the mandatory safety standard for ATVs because they are missing brake lights, reducing visibility of the youth ATV to other vehicles, posing a deadly crash hazard.

  Unclassified

• Medical Device Recall · June 25, 2026

  Pride Mobility Products Corp.

  Brand Name: Quantum Rehab Product Name: Quantum 4Front 2HD Model/Catalog Number: Quantum 4Front 2HD Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 89

  If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

  Class II

• Food Recall · June 25, 2026

  Publix Super Markets, Inc.

  Organic Whole Blueberries, Net Wt 10 oz (284g) plastic bag, packed in 8 bags per case of 10 oz each. Keep Frozen UPC 41415-06453

  Due to potential E. coli O145:H28 contamination

  Class I

• Drug Recall · June 25, 2026

  Bell Pharmaceuticals, Inc

  Clinere, Carbamide Peroxide, a) 2 bottles of Clinere Carbamide Peroxide (2 x 0.50 mL) 6.5%, 0.5 fl. oz. (15 mL); b) 1 bottle of Clinere Carbamide Peroxide (0,50 fl. oz. (15 mL), Dist. by: Quest Produc

  SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

  Class II

• Consumer Product Recall · June 25, 2026

  Lesonic Technology Co., Ltd., dba Small Fish, of China

  Small Fish Montessori Busy Board Toys

  The busy boards violate the mandatory safety standard for toys because magnets can detach, posing a deadly ingestion hazard. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

  Unclassified

• Consumer Product Recall · June 25, 2026

  Shenzhen Qicheng Trading Co., Ltd., dba Carina and Rambo, of China

  Raychy Children's Light Sneakers Unisex

  The recalled sneakers violate the mandatory standard for consumer products with button cell and coin batteries because the lithium coin 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 · June 25, 2026

  Southern Telecom Inc., of New York

  Lomi Roll-On Waxing Kits

  The roll-on warmers' power cord can overheat and short circuit, posing a risk of serious injury or death from fire, burn and electrical shock hazards.

  Unclassified

• Drug Recall · June 25, 2026

  Bell Pharmaceuticals, Inc

  TopCare Health, CARBAMIDE PEROXIDE 6.5%, 0.5 FL OZ (15 mL) a) Kit - WASHER BULB & DROPS INCLUDED (NDC 36800-835-33); b) 1 bottle (NDC 36800-835-34), DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELK GROVE VILL

  SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

  Class II

• Consumer Product Recall · June 25, 2026

  Treatlife Technology Co. Ltd., of China

  Treatlife Smoke and Carbon Monoxide (CO) Detectors

  The recalled detectors can fail to alert consumers of a fire, posing a risk of serious injury or death from smoke inhalation or burns.

  Unclassified

• Medical Device Recall · June 25, 2026

  C.R. Bard Inc

  Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Foley Catheter REF: 947314 947316 947318 UDI codes: 00801741024924¿ 10801741024921 00801741024931¿ 108017410249

  Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

  Class II

• Medical Device Recall · June 25, 2026

  Pride Mobility Products Corp.

  Brand Name: Quantum Rehab Product Name: Quantum Rival Model/Catalog Number: Quantum Rival Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Co

  If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

  Class II

• Medical Device Recall · June 25, 2026

  Pride Mobility Products Corp.

  Brand Name: Quantum Rehab Product Name: Q6 Edge 4 Model/Catalog Number: Q6 Edge 4 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component:

  If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

  Class II

• Consumer Product Recall · June 25, 2026

  Daikin Comfort Technologies Manufacturing, Inc., of Houston, Texas

  Amana Window-Room-Air-Conditioners (WRAC) and Through the Wall (TTW) air conditioners or heat pumps

  The heating element can remain energized during a ground fault, despite being turned off, posing a risk of fire or burn injury to consumers.

  Unclassified

• Consumer Product Recall · June 25, 2026

  ABGA Advanced Trading Co., Ltd., of Walnut, California

  Honlyne LED Party Favors

  The LED party favors violate the mandatory safety standard for consumer products because the battery compartment within the light-up products contains button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

  Unclassified

• Medical Device Recall · June 25, 2026

  Pride Mobility Products Corp.

  Brand Name: Quantum Rehab Product Name: R-TRAK Model/Catalog Number: R-TRAK Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Contr

  If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

  Class II

• Medical Device Recall · June 25, 2026

  Pride Mobility Products Corp.

  Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.38

  If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

  Class II

• Food Recall · June 25, 2026

  Publix Super Markets, Inc.

  Organic Whole Mixed Berries, Net Wt. 48 oz (3Lb) plastic bag. packed in 6 bags per case of 10 oz each. Keep Frozen. UPC 41415-12153

  Due to potential E. coli O145:H28 contamination

  Class I

• Medical Device Recall · June 25, 2026

  C.R. Bard Inc

  Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes: 00801741024801¿ 10801741024808 00801741024818¿ 10801741024815 00801741024

  Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

  Class II

• Food Recall · June 25, 2026

  Fresh & Ready Foods LLC

  Fresh to You Burger Chicken Fillet, SKU 10150, Net wt. 5oz. Product is refrigerated. UPC 1 00000 01015 0. Manufactured By LPK1 Renton, WA. Product was not sold at retail stores and sold only to emplo

  Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Fillet sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.

  Class I

• Medical Device Recall · June 25, 2026

  C.R. Bard Inc

  Products that contain the Pericare Wipes: (Canada Only) SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300314AC UDI-DI code: 00801741143243 SureStep" Foley Tray System Bardex¿ IC Complet

  Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

  Class II

• Food Recall · June 25, 2026

  Publix Super Markets, Inc.

  Organic Whole Mixed Berries, Net Wt. 10 oz (284 g) plastic bags, packed in 8 bags per case of 10 oz each. Keep Frozen. UPC 41415-06753

  Due to potential E. coli O145:H28 contamination

  Class I

• Medical Device Recall · June 25, 2026

  C.R. Bard Inc

  Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley Catheter REF: A153200 UDI code: 00801741121067¿ 10801741121064 SureStep" Foley Tray System Complete Care¿ Add-A-Fole

  Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

  Class II

• Drug Recall · June 25, 2026

  Bell Pharmaceuticals, Inc

  meijer, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Washer Bulb included, NDC 41250-835-33, DIST. BY MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544.

  SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

  Class II

• Medical Device Recall · June 25, 2026

  Pride Mobility Products Corp.

  Brand Name: Quantum Rehab Product Name: Quantum Outback Model/Catalog Number: Quantum Outback Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860

  If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

  Class II

• Food Recall · June 25, 2026

  Publix Super Markets, Inc.

  Organic Whole Blueberries, Net Wt. 48 oz (3Lb) plastic bag, packed in 6 bags per case of 10 oz each. Keep Frozen. UPC 41415-12053

  Due to potential E. coli O145:H28 contamination

  Class I

• Drug Recall · June 25, 2026

  Bell Pharmaceuticals, Inc

  GOOD NEIGHBOR PHARMACY, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), a) Kit - Washer Bulb Included, (NDC 46122-556-05); b) 1 bottle (NDC 46122-557-05), Distributed by: AmerisourceBergen, 1 West First A

  SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

  Class II

• Drug Recall · June 25, 2026

  Bell Pharmaceuticals, Inc

  Foster & Thrive, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), NDC 70677-1154-01, Distributed by: McKesson Corp., via SSSL, Memphis, TN 38141.

  SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

  Class II

• Food Recall · June 25, 2026

  GELLERT GLOBAL GROUP

  Fusia, Asian Inspirations, Kimchi & Tofu Kimbap, 8.1 OZ (230 g), Paper Film Wrapper, 12 packages per case , 6 ea: Kimchi & Tofu Kimbap / 6 ea Spicy Tuna with Gochujang Kimbap, Keep Frozen-Do Not Th

  Undeclared Allergen (Fish)

  Class I

• Medical Device Recall · June 24, 2026

  Covidien, LP

  Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU 75CM C14 88861799-31

  Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if in ophthalmic utilization, or prolonged surgery.

  Class II

• Medical Device Recall · June 24, 2026

  Maquet Critical Care AB

  Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530 Flow-i C40 6888540 Flow-c 6887700 Flow-e 6887900

  Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient receiving insufficient anesthesia and may lead to intraoperative awareness.

  Class II

• Medical Device Recall · June 24, 2026

  Covidien, LP

  V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22 GS-25 VLOCM0436 VLOCM0436 VLOCM0003 V-LOC* 90 4-0 CLR 15CM P12X12 VLOCM0003 VLOCM0013 V

  Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if in ophthalmic utilization, or prolonged surgery.

  Class II

• Medical Device Recall · June 24, 2026

  Medtronic Perfusion Systems

  EOPA 3D Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 78222

  Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dysfunction.

  Class II

• Medical Device Recall · June 24, 2026

  Medtronic Perfusion Systems

  EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77722

  Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dysfunction.

  Class II

• Vehicle Recall · June 24, 2026

  Ford Motor Company

  2023 FORD BRONCO, 2024 FORD BRONCO

  A detached fender flare can become a road hazard and increase the risk of a crash.

  Unclassified

• Medical Device Recall · June 24, 2026

  Covidien, LP

  Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX

  Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if in ophthalmic utilization, or prolonged surgery.

  Class II

• Medical Device Recall · June 24, 2026

  Medtronic Perfusion Systems

  EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77622

  Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dysfunction.

  Class II

• Medical Device Recall · June 24, 2026

  ICU Medical Inc.

  Hotline Fluid Warming Set, single use device, is designed to warm blood and intravenous fluids and deliver them to the patient's intravenous access site at normothermic temperatures under gravity flow

  ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate solvent application at the tubing to return connector bond.

  Class II

• Medical Device Recall · June 24, 2026

  Medtronic Perfusion Systems

  EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77522

  Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dysfunction.

  Class II

• Food Recall · June 24, 2026

  Lehi Valley Trading Company, Inc

  High Valley Orchard Chocolate Covered Raisins, net wt. 15oz. per package, each case contains 12/15oz. bags. Product is packaged in clear plastic container. UPC on retail container: 0 952348 80170 0.

  Undeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packaging.

  Class I