The Recall Desk

Archive

June 2025 recalls

524 recalls were announced in June 2025.

What the numbers show

Critical
6
Severe
230
High
195
Moderate
85
Low
8

Of the 524 recalls this month scored against our rubric, 1% are Critical, 44% are Severe.

1–100 of 524

  • SevereNHTSA·25V434000·2025-06-30

    Volkswagen chassis, brake and suspension bolts may be incorrectly tightened

    Volkswagen is recalling certain 2023-2025 Atlas, Atlas Cross Sport and 2023-2024 ID.4 vehicles because bolts on the chassis, brake system and suspension may not have been correctly tightened in manufacturing.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ID.4, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V445000·2025-06-27

    Orange EV Recalls HUSK-E Trucks for Electrical Fire Risk

    Orange EV is recalling 2023-2025 HUSK-E terminal trucks because an incorrect washer size installed during a previous repair can cause electrical arcing and increase the risk of fire.

    Product
    ORANGE EV — ORANGE EV HUSK-E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V437000·2025-06-27

    Nissan and Infiniti VC-Turbo engine bearings may cause engine failure

    Nissan is recalling certain 2019-2024 Rogue, Altima, Infiniti QX50 and QX55 vehicles with VC-Turbo engines because engine bearing defects can lead to engine failure and, if the block is breached, an engine fire.

    Product
    NISSAN — NISSAN, INFINITI ROGUE, QX50, ALTIMA, QX55
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V443000·2025-06-27

    Ford Recalls 2017 GT Models for Rear Wing Hydraulic Leak Risk

    Ford is recalling 2017 GT vehicles previously repaired under recall 18V707 because the rear wing valve block may leak hydraulic fluid, increasing fire risk.

    Product
    FORD — FORD GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V428000·2025-06-27

    Audi Recalls 2025 E-Tron GT Vehicles Due to Suspension Strut Defect

    Volkswagen Group of America is recalling 2025 Audi E-Tron GT vehicles because a retaining ring on the front suspension strut may come loose, potentially causing air loss and loss of vehicle control.

    Product
    AUDI — AUDI E-TRON GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V438000·2025-06-27

    Ford Recalls 2025 F-150 Lightning BEV Due to Brake Hose Bracket Issue

    Ford is recalling 2025 F-150 Lightning BEV vehicles because front brake jounce hose bracket screws may loosen, causing a brake fluid leak that increases stopping distance.

    Product
    FORD — FORD F-150 LIGHTNING BEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V439000·2025-06-27

    Ford Expedition and Navigator passenger airbags may deploy with excessive force

    Ford is recalling certain 2025 Navigator and Expedition vehicles because the passenger side airbag may have been manufactured incorrectly and can deploy with excessive force during a crash.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V431000·2025-06-27

    Newmar motorhome baggage door skins can separate from the door frame

    Newmar is recalling certain 2016-2024 King Aire, 2023-2024 London Aire and Essex motorhomes because the baggage door skins may come loose and separate from the door frame.

    Product
    NEWMAR — NEWMAR KING AIRE, ESSEX, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V440000·2025-06-27

    Freightliner Recalls 2026 Cascadia Fifth Gen Trucks for Fuel Line Routing Defect

    Daimler Trucks North America is recalling 2026 Freightliner Cascadia Fifth Gen trucks because an incorrectly routed fuel line can damage brake lines and wiring, increasing crash and fire risks.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA FIFTH GEN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V441000·2025-06-27

    Ford Recalls 2022 Mustang Mach E Vehicles for Battery Contactor Overheating

    Ford is recalling 2022 Mustang Mach E vehicles with extended range batteries because high voltage contactors may overheat, potentially causing loss of drive power and increasing crash risk.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V442000·2025-06-27

    Ford rearview cameras may show a blank or persistent image

    Ford is recalling a wide range of 2018-2024 vehicles because a software error may cause the rearview camera to display a blank image, or leave the image on screen after backing has ended.

    Product
    FORD — FORD, LINCOLN EXPLORER, EXPEDITION, EDGE, ECOSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V444000·2025-06-27

    Oshkosh Recalls 2025 NGDV Vehicles for Detaching Air Bag Warning Label

    Oshkosh is recalling 2025 NGDV and NGDV Electric vehicles because the air bag warning label on the sun visor may detach, failing federal safety standards.

    Product
    OSHKOSH — OSHKOSH NGDV ELECTRIC, NGDV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V417000·2025-06-27

    Bowlus trailer manual omits hitch bolt retightening from maintenance schedule

    Bowlus is recalling certain trailers with an elongated hitch because the owner's manual does not include instructions to retighten the two hitch bolts in the maintenance schedule.

    Product
    BOWLUS — BOWLUS ENDLESS HIGHWAYS, TERRA FIRMA, VOLTERRA, RIVET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·024-2025·2025-06-27

    Gaiser's Recalls Ready-to-Eat Bologna Due to Undeclared Meat Ingredients

    Gaiser's European Style Provisions is recalling approximately 143,416 pounds of ready-to-eat bologna products because they contain undeclared meat or poultry ingredients.

    Product
    Gaiser's European Style Provisions Inc. — Gaiser's European Style Provisions Inc. Recalls Ready-To-Eat Meat and Poultry Bologna Products Due to Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·25357·2025-06-26

    Western Saddle Cinches Recalled Due to Fall and Injury Hazards

    Total Saddle Fit is recalling about 10,000 Shoulder Relief Saddle Cinches because the cinch can come apart and cause the saddle to fall off, posing a fall risk to riders. The company has received 19 reports of this defect, including one incident in which a rider fractured their ribs.

    Product
    Shoulder Relief Saddle Cinches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V432000·2025-06-26

    GM Recalls 2018-2019 Trucks Due to Air Bag Inflator Defect

    General Motors is recalling specific 2018-2019 Chevrolet and GMC trucks because roof-rail air bag inflators may rupture or detach, posing an injury risk.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 2500, SILVERADO 3500, SILVERADO 1500, SIERRA 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V435000·2025-06-26

    Honda Recalls 2024 NC750X Motorcycles Due to Front Tire Defect

    Honda is recalling 2024 NC750X motorcycles because the front tire's inner structure may loosen, potentially causing a loss of vehicle control.

    Product
    HONDA — HONDA NC750X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25361·2025-06-26

    Boyro Baby Walkers Recalled Due to Fall Hazard and Lead Content

    About 1,500 Boyro Baby Walkers (model US-B01) are being recalled because they violate federal safety standards for infant walkers and contain excessive lead. The walkers can fit through doorways and fail to stop at steps, posing a risk of serious injury or death; no injuries have been reported.

    Product
    Boyro Baby Walkers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25362·2025-06-26

    Vevor Single Post Handrails Recalled Due to Welding Failure Injury Hazard

    Sanven Technology (Vevor) is recalling about 360 single post handrails for one or two step stairs because the welding can break while in use, posing an injury hazard. Five incidents of handrails breaking have been reported, including one head injury.

    Product
    Vevor Single Post Handrails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25360·2025-06-26

    LED Fireplace Lanterns Recalled for Coin Battery Ingestion Hazard

    Green Pastures Wholesale is recalling LED Fireplace Lanterns because the remote control's lithium coin battery can be easily accessed by children, creating a serious ingestion hazard. Swallowing coin batteries can cause internal chemical burns and death.

    Product
    LED Fireplace Lanterns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V430000·2025-06-26

    Jeep Grand Cherokee blower motor failure can disable windshield defrosting

    Chrysler is recalling certain 2023 Jeep Grand Cherokee and Grand Cherokee L vehicles because the blower motor may fail, leaving the defrosting and defogging system inoperative. This fails FMVSS 103.

    Product
    JEEP — JEEP GRAND CHEROKEE L, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25359·2025-06-26

    Bell Sports Bicycle Helmets Recalled Due to Head Injury Risk

    Bell Sports is recalling approximately 31,200 bicycle helmets because they fail to meet federal safety standards and may not protect wearers during a crash. Consumers should stop using the helmets immediately and contact Bell Sports for a refund.

    Product
    Bell Sports Bicycle Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V436000·2025-06-26

    Kenworth and Peterbilt trucks with lighting and axle control defect

    PACCAR is recalling 2024–2026 Kenworth and Peterbilt trucks. A software fault may prevent tail brake lights, headlights, reverse lights, and turn signals from illuminating properly, and may cause lift axles to unexpectedly raise or oscillate.

    Product
    PETERBILT — PETERBILT, KENWORTH 589, W990, T880, T680
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V354000·2025-06-26

    Temsa Recalls TS30, TS35, TS45, and TS45E Vehicles Due to Roof Hatch Defect

    Temsa is recalling specific 2022-2025 TS30, TS35, TS45, and TS45E vehicles because an incorrectly installed lock mechanism may cause the roof hatch release handle to break, potentially delaying emergency egress.

    Product
    TEMSA — TEMSA TS45, TS30, TS35, TS45E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25354·2025-06-26

    California Gold Nutrition Iron Supplements Recalled Due to Non-Child-Resistant Packaging

    iHerb is recalling three California Gold Nutrition iron supplement products because their bottles and blister packs do not meet federal child-resistant packaging standards, posing a risk of serious injury or death if swallowed by young children.

    Product
    California Gold Nutrition Iron Supplements: Daily Prenatal Multi, Ultamins Women's Multivitamin, and Ultamins Women's 50+ Multivitamin
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V429000·2025-06-26

    Great Dane Recalls 2026 Champion Trailers Due to Door Bolt Issue

    Great Dane is recalling 2026 Champion dry van trailers because roll-up door operator bolts may not be tightened, increasing the risk of injury.

    Product
    GREAT DANE — GREAT DANE CHAMPION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25353·2025-06-26

    Converta Camping Cots and Suspension Stretchers Recalled for Laceration and Amputation Hazards

    The Coleman Company is recalling Converta camping cots and suspension stretchers because the backrest fold mechanism can pinch fingers, causing lacerations and amputations. Seven finger-pinching incidents have been reported, including two fractured fingers.

    Product
    Converta camping cots and Converta camping suspension stretchers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25706·2025-06-26

    Peg Perego Tatamia 3-in-1 Infant Products Recalled for Suffocation Risk

    Peg Perego is recalling about 950 Tatamia 3-in-1 recliners, swings, and high chairs sold from November 2022 through January 2025 due to suffocation risk and safety standard violations. Consumers should stop using them immediately and contact Peg Perego for a refund.

    Product
    Peg Perego Tatamia 3-in-1 Recliner, Swings and High Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25358·2025-06-26

    Professional's Choice Equine Swivel Port Bits Recalled for Fall Hazard

    Professional's Choice Sports Medicine Products is recalling Swivel Port equine bits from the Bob Avila collection because the bits can break during use, posing a fall hazard to riders. The company has received five reports of bits breaking but no injuries have been reported.

    Product
    Swivel Port equine bits from Bob Avila collection
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25355·2025-06-26

    DR Power Lithium-Ion Battery Packs Recalled for Fire and Burn Hazards

    DR Power is recalling about 13,200 LiPRO rechargeable lithium-ion battery packs (5.0 Ah) because they can short-circuit and ignite, posing fire and burn hazards. The firm has received two reports of fire and/or overheating incidents, though no injuries have been reported.

    Product
    DR Power LiPRO rechargeable lithium-ion battery packs (5.0 Ah)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1944-2025·2025-06-25

    Dexcom G7 Glucose Receiver recalled due to defective foam or assembly error

    Dexcom, Inc. is recalling Dexcom G7 Glucose Receiver units due to defective foam or assembly error that may cause the speaker to lose contact with the circuit board, preventing audible alerts for low or high blood glucose.

    Product
    Dexcom G7 Glucose Receiver, SKUs (part number): STK-AT-011(MT26403-0), STK-AT-012 (MT26403-0), STK-AT-013 (MT26403-0), STK-GT-001 (MT26403-1), STK-GT-008 (MT26403-5), STK-GT-013 (MT26403-1) , STK-GT-019 (MT26403-4) , STK-GT-100 (MT26403-2), STK-GT-109 (MT26403-2) , STK-GT-113 (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1946-2025·2025-06-25

    Dexcom One Continuous Glucose Monitoring System Receiver Speaker Defect

    Dexcom, Inc. is recalling Dexcom One Continuous Glucose Monitoring System receivers due to potential defective foam or assembly errors that may cause the speaker to lose contact with internal components, resulting in missed audible alerts for dangerous blood glucose levels.

    Product
    Dexcom One Continuous Glucose Monitoring System, SKUs(Part Number): STK-DO-006 (MT27409-1), STK-DO-013 (MT27409-1), STK-DO-103 (MT27409-2), STK-DO-109 (MT27409-2)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1945-2025·2025-06-25

    Dexcom One+ Continuous Glucose Monitoring System Receiver Speaker Defect

    Dexcom, Inc. is recalling 26,291 units of the Dexcom One+ Continuous Glucose Monitoring System due to defective foam or assembly errors that may prevent audible alerts for low or high blood glucose levels, potentially leading to seizures, loss of consciousness, or death.

    Product
    Dexcom One+ Continuous Glucose Monitoring System, SKU(Part Number): STK-D7-013 (MT28285-1), STK-D7-014 (MT28285-1), STK-D7-103 (MT28285-2)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0057-2025·2025-06-25

    Ginger Beer Juice Soda Recalled for Potential Salmonella Contamination

    RGB Soda, LLC is recalling Refrigerated Cucumber X Tarragon Ginger Beer distributed in Washington due to potential Salmonella contamination. The affected batches were produced on 11/4/2024 and 11/25/2024.

    Product
    Refrigerated Cucumber X Tarragon Ginger Beer (ginger juice). Product is juice soda and distributed in 5gal. pony keg. The kegs were distributed to the firm's own stores where they were served to glasses. The kegs were labeled with the name of the product and the day it was made.
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·021-2025-EXP·2025-06-25

    Starway Recalls Ineligible Frozen Siluriformes Fish Products Imported from Vietnam

    Starway International Group is expanding a recall for frozen fish products from an ineligible Vietnamese establishment. No adverse reactions have been reported.

    Product
    Starway International Group LLC Expands Recall for Ineligible Frozen Siluriformes Fish Products Imported from Vietnam
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1902-2025·2025-06-25

    Cook Beacon Tip Angiographic Catheters Recalled for Tip Separation Risk

    Cook Incorporated is recalling specific lots of Beacon Tip 5.0 Fr Angiographic catheters due to the risk that the catheter tip may separate during use. The affected catheters were distributed worldwide.

    Product
    Beacon Tip 5.0 Fr Angiographic catheters are designed to facilitate diagnostic and therapeutic procedures. Catheters are available in various configurations. Configurations include different shaft lengths and tip curves and some catheters are manufactured with a hydrophilic coati
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·H-0053-2025·2025-06-25

    Vegetable Bowls and Trays Recalled for Potential Salmonella Contamination

    GBC Food Services is recalling vegetable bowls and vegetable ranch trays due to potential Salmonella contamination. Affected products were purchased between May 8 and May 21, 2025.

    Product
    Vegetable Bowl $5 13oz 850065403380 Purchase Dates: 05/08/2025 to 05/21/2025 Vegetable Bowl $10 26 oz 860010507131 Purchase Dates: 05/08/2025 to 05/21/2025 Vegetable Ranch Tray No Dip Small 19.50 oz 850054894335 Purchase Dates: 05/08/2025 to 05/21/2025 Large Vegetable Tray
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Drugs)·D-0493-2025·2025-06-25

    UMOVY ACIDO HIALURONICO supplement recalled for undeclared prescription drugs

    UMOVY ACIDO HIALURONICO dietary supplement has been recalled because it contains undeclared prescription ingredients Dexamethasone and Diclofenac. The product was marketed without FDA approval.

    Product
    UMOVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7503046054134
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V414000·2025-06-25

    International CV brake pressure sensor can leak fluid causing fire

    International is recalling certain 2019-2025 CV vehicles because the brake pressure sensor assembly may leak brake fluid into the pressure switch and short circuit. Owners are advised to park outside until repaired.

    Product
    INTERNATIONAL — INTERNATIONAL CV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V433000·2025-06-25

    Chevrolet Blazer EV parking brake wiring can trigger or lose the brake

    General Motors is recalling certain 2024-2025 Chevrolet Blazer EV vehicles because a damaged or corroded rear parking brake harness can activate the parking brake while driving, or disable it while parked.

    Product
    CHEVROLET — CHEVROLET BLAZER EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1943-2025·2025-06-25

    Dexcom G6 Glucose Receiver recalled for missed audible alerts

    Dexcom G6 Glucose Receiver units may have defective foam or assembly errors that disable audible alerts for dangerously low or high blood glucose, risking seizures, loss of consciousness, or death.

    Product
    Dexcom G6 Glucose Receiver, SKUs (Part Number): STK-FM-001 (MT27408-1) & STK-FR-001 (MT27408-1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0492-2025·2025-06-25

    UNAVY ACIDO HIALURONICO supplement recalled for undeclared pharmaceutical ingredients

    UNAVY ACIDO HIALURONICO hyaluronic acid supplement is being recalled because it contains three undeclared pharmaceutical ingredients: Dexamethasone, Diclofenac, and Omeprazole. The product was marketed without FDA approval and poses health risks from the unlisted drugs.

    Product
    UNAVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7 503046 054295
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0046-2025·2025-06-25

    Lancaster LF Authentic Greek Salad Kit Recalled for Salmonella Risk

    Reser's Fine Foods is recalling Lancaster LF Authentic Greek Salad Kits distributed in MA and PA because the cucumbers may be contaminated with Salmonella. The kits are implicated in an ongoing Salmonella outbreak.

    Product
    Lancaster LF Authentic Greek Salad Kit, 2/7.125lb. packages, net wt. 14.25lb., Item Code 407079, UPC 13454.38482. This is wholesale kit consisting of pre-packaged components in a corrugated box for assembly by retail delis. Kit contains sealed bags of cut produce (sliced cucum
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0052-2025·2025-06-25

    Cucumber bowls and snack cups recalled due to Salmonella contamination risk

    GBC Food Services, LLC is recalling cucumber products sold between May 8 and May 21, 2025, due to potential Salmonella contamination. Affected products include Cucumber Bowl with Ranch dip, Cucumber Slices with Tajin, and Cucumber with Ranch Snack Cup.

    Product
    Cucumber Bowl with Ranch dip 15oz UPC 850054894519 Purchase Dates: 05/08/2025 to 05/21/2025 Cucumber Slices W/Tajin 10 oz UPC 85005368569 Purchase Dates: 05/08/2025 to 05/21/2025 Cucumber w/ Ranch Snack Cup 9.5 oz UPC 850065403144 Purchase Dates: 05/08/2025 to 05
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·H-0054-2025·2025-06-25

    Ready-to-eat salads recalled for potential Salmonella contamination

    GBC Food Services is recalling multiple ready-to-eat salad products due to potential Salmonella contamination. The affected salads were purchased between May 8 and May 21, 2025.

    Product
    Chef Salad 11oz 850065403328 Purchase Dates: 05/08/2025 to 05/21/2025 Family Cobb Salad 22OZ 850054894625 Purchase Dates: 05/08/2025 to 05/21/2025 Individual Garden Salad 12OZ 850054894618 Purchase Dates: 05/08/2025 to 05/21/2025 Individual Greek Salad 12OZ 850054894649 Purchase
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·H-0056-2025·2025-06-25

    Cucumber Carrot Ranch Pack 20oz recalled for Salmonella contamination

    GBC Food Services is recalling Cucumber Carrot Ranch Pack 20oz due to potential Salmonella contamination. The affected products were purchased between May 8 and May 21, 2025, and distributed across nine states.

    Product
    Cucumber Carrot Ranch Pack 20oz 850065403557 Purchase Dates: 05/08/2025 to 05/21/2025
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·F-0938-2025·2025-06-25

    Afghani Corn Bread Doda Recalled for Undeclared Wheat and Sesame

    Ariana Sweets Inc. is recalling Afghani Corn Bread "Doda" because the product contains undeclared wheat and sesame allergens, which are not listed on the label.

    Product
    AFGHANI CORN BREAD "Doda"; INGREDIENTS: Corn Flour, Sugar, Vegetable Oil, Eggs, Milk, Black Seeds, Caardamom; ALLERGEN STATEMENT: This product contains eggs, milk, and may contain traces of nuts. NET WT 24.0 oz (680g); Keep Cool. Reheat in oven if desired.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1988-2025·2025-06-25

    Optima Coil System embolization coils recalled for defective radiopaque marker

    BALT USA is recalling the Optima Coil System because the radiopaque marker was not visible during angiography and was not manufactured to specification.

    Product
    Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851 OPTI0258BLK 00810068568929 OPTI0212BLK 00810068568912 OPTI0206BLK 00810068568905 OPTI0310BLK 00810068568943 OPTI0320BLK 00810068568950 OPTI0151HSS10 008
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1991-2025·2025-06-25

    ICU Medical Plum Solos Infusion Pump Software Safety Defect Recall

    ICU Medical is recalling Plum Solos infusion pumps (Item 400011001) with software version 1.1.1 due to a workflow that may bypass the Maximum Dose Limit alert, which is designed to prevent overdose. The defect affects 214 units distributed across nine US states and the Philippines.

    Product
    ICU Medical Plum Solos, Item number 400011001; infusion pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0045-2025·2025-06-25

    Big Y Deli Sandwiches Recalled for Salmonella-Contaminated Cucumber

    Big Y Supermarkets has recalled various made-to-order deli sandwiches because cucumbers used in the products were contaminated with Salmonella. The recall affects sandwiches sold on May 20 and 21 at Big Y locations in Massachusetts and Connecticut.

    Product
    Big Y various sandwiches made to order at deli counter (Subs (small, large, supersub), wrap, panini, grinders); UPC Codes: 22172700000, 22178100000, 22247700000, 22314200000, 22314300000, 22314400000, 22314500000, 22314600000, 22314700000, 22314800000, 22314900000, 22315000000,
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1992-2025·2025-06-25

    Fresenius 5008X HDF Hemodialysis Blood Tubing Sets recalled for potential blood leaks

    Fresenius Medical Care is recalling 5008X HDF Hemodialysis Blood Tubing Sets due to potential blood leaks between the venous chamber and tubing. The recall affects hemodialysis, hemodiafiltration, hemofiltration, and isolated ultrafiltration procedures nationwide.

    Product
    5008X HDF Hemodialysis Blood Tubing Set, 24 units per case, with the following models: a. 5008X Standard HDF Bloodline, Model Number: 03-5100-7. b. 5008X Standard HDF Bloodline w/CLIC, Model Number: 03-5100-7C. c. 5008X Standard HDF Bloodline w/ Twister, Model Number: 03-5150-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1981-2025·2025-06-25

    UROSKOP Omnia X-ray System Model 10094910 Frequency Inverter Overheating Recall

    Siemens is recalling 95 units of the UROSKOP Omnia X-ray system nationwide due to a resistor in the frequency inverter that may overheat and potentially ignite the plastic housing.

    Product
    UROSKOP Omnia. Model Number: 10094910
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1977-2025·2025-06-25

    Fitbone Trochanteric Nail may bend during insertion and require replacement

    Orthofix Srl is recalling Fitbone Trochanteric Nails (Lot B4771336 and B4771337) because the implant may bend at the distal tail during insertion, potentially requiring replacement.

    Product
    REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1987-2025·2025-06-25

    Biomet 3i Certain-Compatible 4.1mm Milled Titanium Dental Abutments

    Preat Corp is recalling Biomet 3i Certain-compatible 4.1mm Milled Titanium Abutments (Model 9001767-F) due to manufacturing defects that may cause improper screw engagement. The screw seat was positioned too high, potentially compromising the attachment of mating screws to the underlying implant.

    Product
    Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single-unit or multi-unit prosthetic restorations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1982-2025·2025-06-25

    Siemens UROSKOP Omnia Max frequency inverter fire risk recalled

    Siemens is recalling UROSKOP Omnia Max medical devices due to a resistor in the frequency inverter that may overheat and ignite the plastic housing. Twenty-five units distributed nationwide are affected.

    Product
    UROSKOP Omnia Max. Model Number: 10762473
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0055-2025·2025-06-25

    Fruit and Veg Tray 64oz Recalled for Potential Salmonella Contamination

    GBC Food Services, LLC is recalling Fruit and Veg Tray 64oz products due to potential Salmonella contamination. The affected products were distributed to multiple states and purchased between May 8 and May 21, 2025.

    Product
    Fruit and Veg Tray 64oz 850065403748 Purchase Dates: 05/08/2025 to 05/21/2025
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-1980-2025·2025-06-25

    Portable Oxygen Concentrator with Erroneous Calibration Values

    Ohio Medical Corporation is recalling 36 units of the GCE HEALTHCARE Zen-O lite portable oxygen concentrator due to erroneous calibration values that may cause the device's alarm for low oxygen purity to function incorrectly as the device ages.

    Product
    GCE HEALTHCARE Zen-O lite, Portable Oxygen Concentrator, Model RS-00608-X-S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1990-2025·2025-06-25

    ICU Medical Plum Duo Infusion Pump Software Dose Limit Issue

    ICU Medical is recalling Plum Duo infusion pumps with software version 1.1.1 because a workflow may bypass the Maximum Dose Limit alert, potentially allowing unsafe medication doses to be programmed.

    Product
    ICU Medical Plum Duo, Item numbers: 1) 400020401, 2) 400021001 , and 3) 400021003; infusion pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1989-2025·2025-06-25

    Prestige Coil System implantable devices recalled for manufacturing defect

    BALT USA is recalling Prestige Coil System implantable embolization devices because radiopaque markers on some units were not manufactured to specification and were not visible during angiography.

    Product
    Prestige Coil System REFs/UDI-DI codes: PRES0153CXPPLT 00810068567311 PRES1045CPKPLT 00810068567663 PRES1245CPKPLT 00810068567694 PRES1445CPKPLT 00810068567724 PRES0103CXPPLT 00810068567304 PRES2512CXPPLT 00810068567397 PRES0258CXPPLT 00810068567380 PRES0212CXPPLT 0081006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1985-2025·2025-06-25

    Surgical Mesh Recalled for Potential Residual Adhesive Material

    Chamberlain Technologies LLC is recalling SURGIMESH XB surgical mesh due to potential residual adhesive material on the mesh surface. The affected product was distributed to Illinois, Nebraska, and California.

    Product
    SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·H-0047-2025·2025-06-25

    Pain Train Salsa Creamy Avocado Spicy Recalled for Undeclared Milk

    Pain Train Salsa - Creamy Avocado Spicy (12 oz, refrigerated) is recalled due to undeclared milk allergen. The product was distributed in Texas.

    Product
    Pain Train Salsa - Creamy Avocado Spicy Refrigerated. Shelf Life 90 days. 12 oz Flexible Plastic containers. UPC: 19589339802
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0050-2025·2025-06-25

    Great Plains Bentonite Herbal Detox Capsules Recall

    Yerba Prima Inc is recalling Great Plains Bentonite + Herbal Detox Capsules due to potential contamination with Pseudomonas aeruginosa. Affected bottles have Lot # 05051 with expiration date 02/2028.

    Product
    Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle, white plastic cap and tamper proof seal. Case GTIN code:100 46352 00518 5. Retail package UPC code: 0 46352 00518 8. Yerba Prima, Inc. 740 Jefferson Ave Ashland, Oregon 97520 USA
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·H-0048-2025·2025-06-25

    Topo Chico Mineral Water Recalled for Pseudomonas Contamination

    The Coca-Cola Company is recalling Topo Chico Mineral Water 16.9 fl oz bottles due to potential Pseudomonas contamination. Product was distributed to Arizona, Louisiana, New Mexico, Nevada, and Texas.

    Product
    Topo Chico MINERAL WATER CARBONATED 16.9 FL OZ (500mL) Bottle UPC 0 21136 18061 9, Case UPC 0 21136 18062 6 MADE IN MEXICO BY: CIA. TOPO CHICO, S. DE R.L. DE C.V. MONTERREY NO. 6500 COL. TOPO CHICO, MTY.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1984-2025·2025-06-25

    Surgical Mesh Product Recalled Due to Residual Adhesive Material

    Chamberlain Technologies is recalling SURGIMESH XB surgical mesh due to potential residual adhesive material on the mesh surface. The product was distributed to facilities in Illinois, Nebraska, and California.

    Product
    SURGIMESH XB, Polymeric Surgical Mesh, 14m x 15cm Flat Sheet with Silicone Barrier, Model/Catalog Number: Tintra R-1415
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1941-2025·2025-06-25

    Lago X X-ray instrument recall due to labeling discrepancies

    Spectral Instruments Inc is recalling the Lago X X-ray instrument because its safety and manufacturing date labels do not match FDA requirements.

    Product
    Lago X
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1983-2025·2025-06-25

    Surgical Mesh Recalled for Potential Residual Adhesive Material

    Chamberlain Technologies LLC is recalling SURGIMESH WN Polymeric Surgical Mesh due to potential residual adhesive material on the mesh surface. The 60-unit recall affects medical facilities in Illinois, Nebraska, and California.

    Product
    SURGIMESH WN, Polymeric Surgical Mesh, Large Flat Sheet, Model/Catalog Number: T3030
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1993-2025·2025-06-25

    STA-Owren Koller Buffer Solution Recall Due to Clotting Time Concerns

    Diagnostica Stago is recalling STA-Owren Koller buffer solution (Lot 270902) because it may produce shorter clotting times in certain tests, potentially leading to a 1% overestimate of clotting results.

    Product
    STA - Owren Koller. Model/Catalog Number: 00360 STA - Owren-Koller is a buffer solution intended for use as a diluent for reagents and human plasmas in coagulation tests performed with analyzers of the STA-R, STA Compact, STA Satellite and ST art families.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1978-2025·2025-06-25

    MiniDock Integrated Nucleic Acid Testing Device Recall

    Guangzhou Pluslife Biotech is recalling the MiniDock Integrated Nucleic Acid Testing Device (Model PM001) because it was distributed in the U.S. without required FDA premarket authorization.

    Product
    Brand Name: MiniDock Product Name: Integrated Nucleic Acid Testing Device Model/Catalog Number: PM001 Software Version: N/A Product Description: 1. Product Overview 1.1 Product Name: Integrated Nucleic Acid Testing Device Brand Name: MiniDock 1.2 Model: PM001 2.Pr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0051-2025·2025-06-25

    Pizza Shoppe Pink Stuff Creamy Garlic Salad Dressing Recalled for Potential Spoilage

    La Fontanella Food Products LLC is recalling Pizza Shoppe The "Pink Stuff" World-Famous Creamy Garlic Salad Dressing (12 oz bottles) due to detected increased lactic acid levels indicating potential product spoilage.

    Product
    Pizza Shoppe The "Pink Stuff" World-Famous Creamy Garlic Salad Dressing, net wt. 12oz, UPC 896537002019 packaged in clear plastic bottle with twist lid. Bottles are packed 6/case.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1979-2025·2025-06-25

    Pluslife SARS-CoV-2 Card Test Kits Recalled for Lack of FDA Authorization

    Pluslife SARS-CoV-2 Card nucleic acid testing kits were distributed in the U.S. without required FDA premarket authorization. The FDA is recalling approximately 1,850 boxes distributed nationwide and internationally.

    Product
    Brand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid Testing Card Model/Catalog Number: RM1010202 Software Version: N/A Product Description: 1. Product Overview Product Name: SARS-CoV-2 Nucleic Acid Testing Card Trade Name: Pluslife SARS-CoV-2 Card 2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0472-2025·2025-06-25

    Gentamicin Injection Pediatric Vials Recalled for Failed Stability Tests

    Eugia US LLC is recalling Gentamicin Injection, USP (Pediatric), 20 mg per 2 mL due to failed color absorbance test results during 12-month stability analysis. The recall affects 48,000 vials distributed nationwide.

    Product
    GENTAMICIN — GENTAMICIN (GENTAMICIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0471-2025·2025-06-25

    Amazon Basic Care Acetaminophen 325 mg Tablets Recalled Due to Discoloration

    Aurobindo Pharma USA Inc is recalling Amazon Basic Care Acetaminophen 325 mg tablets due to confirmed consumer complaints of brown surface discoloration on tablets, a cGMP deviation.

    Product
    AMAZON BASIC CARE ACETAMINOPHEN — AMAZON BASIC CARE ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0098-2025·2025-06-25

    CPK Tequila Lime Base Recalled for Possible Wood Contamination

    Bakkavor Foods USA, Inc. is recalling CPK Tequila Lime Base because the product may contain pieces of wood. The affected 1 lb bags were distributed to Alabama, California, Florida, and Maryland.

    Product
    CPK TEQUILA LIME BASE ALLERGENS: MILK NET WEIGHT: 1 LB Case UPC FG15453558 Manufactured for California Pizza Kitchen, Inc.***Los Angeles, CA
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1986-2025·2025-06-25

    Surgical Mesh Recalled Due to Residual Adhesive Material Concern

    Chamberlain Technologies LLC is recalling SURGIMESH WN polymeric surgical mesh due to potential residual adhesive material on the mesh surface. The recall affects 20 units distributed to Illinois, Nebraska, and California.

    Product
    SURGIMESH WN, Polymeric Surgical Mesh, 14cm x 15cm Flat Sheet, Model/Catalog Number: T1415
    Category
    Medical Device
    Distribution
    3 states
  • LowFDA (Devices)·Z-1976-2025·2025-06-25

    AcoSound LW12-BTE-M Hearing Aid Labeling and UDI Information Errors

    Hangzhou AcoSound Technology Co., Ltd. is recalling 120 units of the AcoSound Model LW12-BTE-M hearing aid due to labeling errors, including incorrect manufacturer attribution, missing manufacturer business address, and incomplete UDI information.

    Product
    AcoSound. Model Number: LW12-BTE-M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V380000·2025-06-23

    GEM Recalls 2022-2025 Electric Vehicles Due to Ball Joint Separation Risk

    GEM is recalling 2022-2025 e2, e4, e6, and eLXD vehicles because improperly tightened fasteners may cause the front lower ball joint to separate, potentially leading to a loss of steering control.

    Product
    GEM — GEM E4, E6, ELXD, E2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V384000·2025-06-23

    Keystone Recalls 2025 Toy Haulers Due to Missing Rear Gate Pins

    Keystone is recalling 2025 Carbon, Fuzion, and Raptor toy haulers because missing rear gate pins or leg support brackets may allow the gate to shift, increasing injury risk.

    Product
    KEYSTONE — KEYSTONE CARBON, FUZION, RAPTOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V326000·2025-06-23

    Western Star battery to starter stud can short circuit

    Daimler Trucks is recalling certain 2020-2026 Western Star 49X and 2021-2026 47X vehicles because a stud connecting the battery to the starter at the frame rail may have been incorrectly installed.

    Product
    WESTERN STAR — WESTERN STAR 47X, 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V425000·2025-06-20

    Travel trailer patio door transit latch cannot be opened from inside

    Forest River is recalling certain 2025-2026 Wildwood and Salem travel trailers because the exterior transit latch on the rear patio door cannot be unlocked from inside the vehicle.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-06202025-01·2025-06-20

    USDA Issues Public Health Alert for Uninspected Thompson's Meat Sauce Products

    USDA FSIS issued a public health alert for Thompson's meat sauce products produced without federal inspection. Consumers in Illinois and Indiana are urged to discard the items.

    Product
    FSIS Issues Public Health Alert for Meat Sauce Products Produced Without the Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·25V423000·2025-06-20

    2026 Forest River Spirit travel trailers recalled for defective safety chains

    Forest River is recalling certain 2026 Spirit travel trailers because the installed safety chains may not meet the actual Gross Vehicle Weight Rating, posing a risk of trailer separation from the tow vehicle.

    Product
    FOREST RIVER — FOREST RIVER SPIRIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V424000·2025-06-20

    2026 Forest River Sabre Fifth Wheel Griddle Fire Risk Recall

    Forest River is recalling 2026 Sabre fifth wheel recreational trailers because the exterior griddle may be incorrectly installed, allowing it to be stowed while still connected to LPG, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER SABRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V385000·2025-06-19

    Vanguard Recalls 2021-2023 VXP Trailers Due to Hook Box Defect

    Vanguard is recalling 2021-2023 VXP 28-Foot Pup trailers because the pintle hook box assembly may crack or break, reducing stability while being towed.

    Product
    VANGUARD — VANGUARD VXP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V422000·2025-06-19

    Honda Recalls 2013 Accord Vehicles for Driveshaft Corrosion Risk

    Honda is recalling 2013 Accord vehicles with 4-cylinder engines and CVTs in 23 states and D.C. because the driveshaft may corrode and break, potentially causing a loss of drive power or vehicle rollaway.

    Product
    HONDA — HONDA ACCORD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V419000·2025-06-19

    Subaru Forester child seat anchor bolts may come loose

    Subaru is recalling certain 2025 Forester vehicles because the child seat anchor bolts may have been improperly tightened, allowing them to come loose.

    Product
    SUBARU — SUBARU FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V405000·2025-06-19

    Shyft Recalls 2024-2025 Utilimaster Aeromaster for Camera Display Defect

    Shyft Group is recalling 2024-2025 Utilimaster Aeromaster vehicles because the 360-degree camera monitor may not display the correct image at startup, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER AEROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V421000·2025-06-19

    Supreme Recalls 2025 Wabash Trucks Due to Liftgate Pin Seizure Risk

    Supreme is recalling 2025 Wabash trucks because insufficient lubrication on the liftgate pin may cause it to seize, leading to liftgate failure and injury risk.

    Product
    SUPREME — SUPREME WABASH TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25345·2025-06-18

    TADAKAZU Baby Loungers Recalled for Suffocation Fall and Entrapment Hazards

    TADAKAZU Baby Loungers violate federal infant sleep product standards, posing risks of suffocation, falls, and entrapment. The CPSC recommends immediate discontinuation and contact with TADAKAZU for refund.

    Product
    TADAKAZU Baby Loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25342·2025-06-18

    AstroAI 4-Liter/6-Can Minifridges Recalled Due to Fire and Burn Hazards

    AstroAI is recalling approximately 249,100 minifridges because the electrical switch can short circuit, causing fires and burn hazards. At least 70 incidents of smoking, burning, melting, or fire have been reported, including two fires that caused more than $360,000 in property damage.

    Product
    4 Liter/6 Can Minifridges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V413000·2025-06-18

    Mazda CX-50 airbag module software may cause improper deployment

    Mazda is recalling certain CX-50 Hybrid and CX-50 vehicles because incorrectly configured module software may cause the airbag to deploy improperly. All affected vehicles are under dealer control.

    Product
    MAZDA — MAZDA CX-50 HYBRID, CX-50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1952-2025·2025-06-18

    Tecfen Medical 2.8mm Slit Knife Angled Sterility Assurance Recall

    Tecfen Medical is recalling 2.8mm Slit Knife, Angled (Model QKN2808) ophthalmic surgical instruments due to sterility assurance concerns. Affected units were distributed in the US and internationally.

    Product
    Brand Name: Tecfen Medical Product Name: 2.8mm Slit Knife, Angled Model/Catalog Number: QKN2808 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile (gamma radiation) and packaged individually in Tyvek 1059B. Slit knive
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0033-2025·2025-06-18

    Jean's Classy Fresh Salsa Hot recalled due to Salmonella contamination

    TGD Cuts, LLC is recalling Jean's Classy Fresh Salsa, Hot (6/12 oz. plastic tubes) due to Salmonella contamination. The affected product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.

    Product
    Jean's Classy Fresh Salsa, Salsa, Hot 6/12 oz., Plastic tube, 6 per case .
    Category
    Food
    Distribution
    5 states

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