Latest U.S. recalls (page 4)
500 recalls.
- VOCSN+Pro recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - BAMAMON Recalls LED Projecting Finger Light Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Consumer productReported October 22, 2026 · None reported. - Lithonia Lighting Recalls RSX Luminaires with Adjustable Tilt Arm Mountings Due to Risk of Serious Injury from Impact Hazard
Consumer productReported October 22, 2026 · The knuckle of the recalled adjustable tilt arm mountings can fail, allowing the luminaire to fall from the mounting arm, posing a risk of serious injury due... - Costway Recalls Convertible High Chairs Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory Standard for High Chairs
Consumer productReported October 22, 2026 · The convertible high chairs violate the mandatory safety standard for high chairs because they do not contain a passive restraint system and a child can slip... - VQQQ Gas Patio Heaters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Consumer productReported October 22, 2026 · Components on the recalled patio heaters can malfunction, causing gas to be released, posing a risk of serious injury or death from fire and burn hazards. - FoShanShiNanHaiQuNuoAiTongZhuangShangHang Recalls CIYTI Light-Up Princess Costumes Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Consumer productReported October 22, 2026 · The costumes violate the mandatory safety standard for toys because the button cell batteries can be accessed easily by children, posing a deadly ingestion... - Pur Aqua Sparkling Frost Cherry Limeade 17 oz. recall (Refresco Beverages US Inc)
FoodClass IIIReported October 21, 2026 · May contain undeclared aspartame. - Stewarts Shops Vanilla Heavenly Medley 1/2 Gallon recall (Stewart's Shops Corp.)
FoodClass IIReported October 21, 2026 · Foreign object: May contain pieces of metal - Stewarts Shops Vanilla chocolate Strawberry Ice Cream 1/2 gallon recall (Stewart's Shops Corp.)
FoodClass IIReported October 21, 2026 · Foreign object: May contain pieces of metal - Deano's Pasta recall (DEANO'S PASTA)
FoodClass IReported October 21, 2026 · Undeclared Lobster - Made From Plants recall (DARING FOODS INC)
FoodClass IIReported October 21, 2026 · defective packaging; packaging can rupture/explode during cooking. - J. HIGGS Loaded Bacon & Cheddar Potato Chips recall (Saratoga Potato Chips LLC)
FoodClass IIReported October 21, 2026 · Undeclared soy. - Holsum Spinach Flour Tortillas Large recall (Holsum De Puerto Rico, Inc.)
FoodClass IIReported October 21, 2026 · Undeclared colors (FD&C Blue No. 1 and FD&C Yellow No. 5) - Metoclopramide Tablets recall (American Health Packaging)
DrugClass IIReported October 21, 2026 · Presence of Foreign Tablets/Capsules - Sermorelin recall (Houston Rx LLC)
DrugClass IIReported October 21, 2026 · Lack of process control - Tirzepatide/Niacinamide 2mL vial recall (Houston Rx LLC)
DrugClass IIReported October 21, 2026 · Lack of assurance of sterility. - Hydrocortisone Sodium Succinate for Injection recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIReported October 21, 2026 · Failed Impurities/Degradation Specifications. - Metoclopramide Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported October 21, 2026 · Presence of Foreign Tablets/Capsules - The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists recall (Radiometer Medical ApS)
Medical deviceClass IIReported October 21, 2026 · In vitro diagnostic analyzer had a risk of potentially inaccurate results requiring changes to instructions for use and: 1) Sample types, including whole blood... - Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Discrepancy in the shelf-life of a component - Vinyl Instrument Guards recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported October 21, 2026 · Labeling not compliant with 21 CFR 801 and steam sterilization IFU has been updated. - Scout MD recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported October 21, 2026 · The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use. - IntelePACS recall (INTELERAD MEDICAL SYSTEMS INCORPORATED)
Medical deviceClass IIReported October 21, 2026 · Following a Chromium-based web-browser, report and displayed images may not match. - Convenience Kits containing CONMED AirSeal Access Ports KIT ROBOTICS UROLOGY... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports CHN GYN ONCOLOGY ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports GENERAL DAVINCI ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports HERNANDEZ DAVINCI ACC... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Medline surgical convenience kits labeled as: 1) SPINAL CDS recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: OPEN HEART recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) NEURO-SPINE BASIN PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A & recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) CV BASIN PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) MAIN/LAPAROSCOPY TRANSPLA PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) EAR recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: VEIN HARVESTING PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) VEIN HARVESTING PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - 1) Product Name AUD OPEN HEART PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: CABG AUXILIARY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - TS Misc. Instruments Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - Triathlon Hinge Femoral Prep Tray. Catalog Number: 6543-6-514. recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - TS Femoral Prep Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - TS Universal Baseplate Finishing Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - Williams Cystoscopic Injection Needles recall (Cook Incorporated)
Medical deviceClass IIReported October 21, 2026 · The female Luer lock adapter component in the affected device lots may not have been correctly seated due to misalignment and inadequate torquing during... - LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762. recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIIReported October 21, 2026 · In kit sub-lot 2530M-01 the date of expiration printed on the outer labeling may indicate the wrong expiration date of July 22, 2026 while the correct... - IQ200 SPRINT recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported October 21, 2026 · The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however... - DxU 840m Iris recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported October 21, 2026 · The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however... - MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control recall (Microgenics Corporation)
Medical deviceClass IIReported October 21, 2026 · Vial-to-vial variability in MAS¿ Omni"IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, Lot OPRO29061A results in low Parathyroid Hormone... - Generic Name: GORE VIABIL Short Wire Biliary Endoprosthesis recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported October 21, 2026 · The potential for the devices to be mislabeled with the incorrect length. - REF: P65 ST862 CoLag SCREW recall (In2bones USA, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to labeling error, bone screws specified as fully threaded, are actually partially threaded screws. - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture recall (Ethicon, LLC)
Medical deviceClass IIReported October 21, 2026 · Silk sutures, indicated for use in cardiovascular, ophthalmic and neurological procedures, packaged with alcohol-based fluid, not part of product design, that... - Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 ... recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported October 21, 2026 · Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift... - Generic Name: BioFire¿ Joint Infection recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel... recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - Generic Name: FilmArray¿ Pneumonia Panel Generic Name: FilmArray¿ Pneumonia Panel ... recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - FORWARD Gunshot Wound Kit recall (INTEGRATED MEDCRAFT LLC)
Medical deviceClass IIReported October 21, 2026 · Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device's sterile pad, potentially causing the... - iFuse TORQ Implant System Model/Catalog Number: 10055T recall (SI-BONE, Inc.)
Medical deviceClass IIReported October 21, 2026 · The pelvic fixation screws failed to meet acceptance criteria for tube packaging seal integrity testing; therefore, sterility assurance cannot be ensured. - Power F2 Powered Fastening System recall (Ferno-Washington Inc)
Medical deviceClass IIReported October 21, 2026 · Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system... - Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack recall (Sarnova HC, Llc)
Medical deviceClass IIReported October 21, 2026 · Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula. - NaviFlex LW Pusher recall (Boston Scientific Corporation)
Medical deviceClass IIReported October 21, 2026 · Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this... - NeuroStar Advanced Therapy System. Contains the NeuroStar HP Coil Assembly Part Number... recall (Neuronetics, Inc.)
Medical deviceClass IIReported October 21, 2026 · Cables are not in conformance with the product specifications required in the production of the HP Coil Assembly. - Brand Name: IOMAX Product Name: IOMAX Cortical Module Model/Catalog Number:... recall (Cadwell Industries Inc)
Medical deviceClass IIReported October 21, 2026 · Stimulator device contains a defective printed circuit board assembly (PCBA) that may cause the device to unintentionally deliver electrical stimulation to the... - BD Phoenix Panel NMIC-306. Catalog Number: 449292. recall (Becton Dickinson & Co.)
Medical deviceClass IIReported October 21, 2026 · Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. - BD Phoenix Panel NMIC-312. Catalog Number: 449082. recall (Becton Dickinson & Co.)
Medical deviceClass IIReported October 21, 2026 · Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. - Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined... recall (Medtronic Sofamor Danek USA Inc)
Medical deviceClass IIReported October 21, 2026 · Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to... - Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined... recall (Medtronic Sofamor Danek USA Inc)
Medical deviceClass IIReported October 21, 2026 · Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related... - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - HemoslL AcuStar HIT-lgG recall (Instrumentation Laboratory)
Medical deviceClass IReported October 21, 2026 · Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples. - HemoslL AcuStar HIT-lgG recall (Instrumentation Laboratory)
Medical deviceClass IReported October 21, 2026 · Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples. - usOpal Recalls Xalirium Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
Consumer productReported October 15, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped... - Primark Recalls 101 Dalmatians Faux Leather Children’s Coin Purses Due to Phthalate Levels and Risk of Ingestion
Consumer productReported October 15, 2026 · The coin purses contain higher phthalate concentration levels. Phthalates can be harmful if young children are exposed to sufficient amounts, including through... - Papablic, of USA Recalls Convertible Bedside Sleepers Due to Risk of Serious Injury or Death from Entrapment, Suffocation and Fall Hazards; Violate Mandatory Standard for Play Yards
Consumer productReported October 15, 2026 · The bedside sleepers with play yard extensions violate the mandatory safety standard for play yards because the mattress can become displaced, causing a baby... - Loving Thyself Rocks Recalls Crystal Glass Cups Due to Risk of Serious Injury from Ingestion and Laceration Hazards
Consumer productReported October 15, 2026 · Glass can break inside the recalled cups while in use, posing a risk of serious injury from ingestion and laceration hazards. - HatsanUSA Recalls Blitz Air Rifles Due to Risk of Serious Injury or Death from Projectile Hazard
Consumer productReported October 15, 2026 · The recalled air rifles can fire unexpectedly when releasing the bolt before the air rifle is fully cocked, posing a risk of serious injury or death from... - 3M Company Recalls Scotch™ Thermal Laminators Due to Risk of Serious Injury or Death from Fire Hazard
Consumer productReported October 15, 2026 · The recalled thermal laminators can overheat, posing a fire hazard. - SIERRA NEVADA CHEESE GRAZIERS RAW MILK SHARP CHEDDAR recall (Sierra Nevada Cheese Company, Inc)
FoodNot Yet ClassifiedReported October 14, 2026 · Potential contamination due to E. coli O26:H11. - Croissant recall (J K Patisserie & Bakery LLC)
FoodClass IIReported October 14, 2026 · Egg was not declared in the Contains statement. - Chocolate Chip Cookies packaged in a cardboard box recall (J K Patisserie & Bakery LLC)
FoodClass IIReported October 14, 2026 · Soy was not declared in the Contains statement. - Lemon Blueberry Loaf packaged in a cardboard box recall (J K Patisserie & Bakery LLC)
FoodClass IIReported October 14, 2026 · Product contains undeclared soybean oil and soy lecithin in the Ingredient Statement. Soy was not declared in the Contains statement. - Saint Francis Apizza Frozen Supreme Pizza recall (Saint Francis Apizza LLC)
FoodClass IIReported October 14, 2026 · Undeclared soy allergen: soybean oil and soy lecithin - Saint Francis Apizza Frozen Mushroom & Onion Pizza recall (Saint Francis Apizza LLC)
FoodClass IIReported October 14, 2026 · Undeclared soy allergen: soybean oil and soy lecithin - Saint Francis Apizza Frozen Cheese Pizza recall (Saint Francis Apizza LLC)
FoodClass IIReported October 14, 2026 · Undeclared soy allergen: soybean oil and soy lecithin - Saint Francis Apizza Frozen Pepperoni Pizza recall (Saint Francis Apizza LLC)
FoodClass IIReported October 14, 2026 · Undeclared soy allergen: soybean oil and soy lecithin - Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC. Product... recall (SWEET SENSI)
FoodClass IIReported October 14, 2026 · Staphylococcus aureus detected in product. - biQ-FEL recall (A&P CREATIONS)
FoodClass IReported October 14, 2026 · Product contains undeclared Sildenafil and Tadalafil. - X10 Natural Enhancement Supplement recall (A&P CREATIONS)
FoodClass IReported October 14, 2026 · Product contains undeclared Sildenafil and Tadalafil. - QUESO PALMITA. Generic Name: Pastel de Queso recall (QUESO PALMITA GP LLC)
FoodClass IIReported October 14, 2026 · Undeclared milk, cheese declared - Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black... recall (GIAS FOOD INC.)
FoodClass IReported October 14, 2026 · Contamination with Listeria monocytogenes - Berlin Seeds Alfalfa Sprouting Seeds recall (Berlin Seeds)
FoodClass IReported October 14, 2026 · Product contains alfalfa seed recalled by the supplier due to potential E. coli and/or Salmonella contamination. - Cranberry Chicken Salad Wedge 4.5 oz package in Wedge plastic and clear container with... recall (FRESHPOINT CENTRAL FLORIDA, INC.)
FoodClass IIReported October 14, 2026 · The chicken salad sandwich has an improperly declared allergen (egg). While egg is included in the ingredients list on the package label, it is not included in... - Donutful Chocolate Dipped Vanilla Cake Donuts - 7.05oz/10ct.Case Configuration 5... recall (The Better Bakehouse Snack Company)
FoodClass IReported October 14, 2026 · Undeclared Milk. - 28 oz. Gatorade Lemon Lime recall (Pepsico Inc)
FoodClass IIReported October 14, 2026 · Undeclared Yellow No. 6 and/or Yellow No. 5 - WinCo Foods Salsa Bean Dip Express Tray is packaged in a foil bottom container with... recall (WinCo Foods LLC)
FoodClass IIReported October 14, 2026 · Bean Dip Trays contains recalled Peperoncini (pepper) which was recalled due to pest issue.