The Recall Desk

Archive

August 2024 recalls

595 recalls were announced in August 2024.

What the numbers show

Critical
16
Severe
134
High
374
Moderate
69
Low
2

Of the 595 recalls this month scored against our rubric, 3% are Critical, 23% are Severe.

401–500 of 595

  • ModerateFDA (Food)·F-1637-2024·2024-08-14

    Maple Infused Simple Syrup Recalled Due to Potential Under-Processing

    Urban River Spirits recalls 3876 bottles of Maple Infused Simple Syrup distributed across multiple states. The product was manufactured in an unlicensed, uninspected facility and may be under-processed.

    Product
    Maple Infused Simple Syrup is a non-alcoholic cocktail mixer. Product is packaged in glass 5oz. bottle and sold under brand Urban River Spirits.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-1617-2024·2024-08-14

    Non-Alcoholic Beverage Mixer Recalled for Potential Under-Processing Concerns

    Urban River Spirits is recalling Watermelon Lemonade Splash non-alcoholic mixer due to potential under-processing. The product was manufactured in an unlicensed, uninspected facility, raising food safety concerns.

    Product
    Watermelon Lemonade Splash is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-2504-2024·2024-08-14

    Soltive Premium SuperPulsed Laser System Wireless Footswitch Pairing Difficulties

    The Soltive Premium SuperPulsed Laser System may experience difficulties pairing its wireless footswitch, potentially delaying surgical procedures. The recall affects units distributed worldwide.

    Product
    Soltive Premium SuperPulsed Laser System, Model TFL-PLS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1633-2024·2024-08-14

    Non-alcoholic cocktail mixer recalled due to unlicensed production facility

    Urban River Spirits is recalling Raspberry and Peach Melody non-alcoholic cocktail mixer due to concerns over potential under-processing. The product was manufactured in an unlicensed and uninspected facility.

    Product
    Raspberry and Peach Melody is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-2506-2024·2024-08-14

    Wireless Footswitch for Soltive Laser System Recalled for Pairing Difficulties

    Olympus Corporation of the Americas is recalling 1,838 units of the Soltive SuperPulsed Laser System Wireless Footswitch due to pairing difficulties that may delay surgical procedures.

    Product
    Soltive SuperPulsed Laser System Wireless Footswitch, Model TFL-AFSWL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1635-2024·2024-08-14

    Cinnamon Infused Syrup Recalled from Unlicensed Manufacturing Facility

    Urban River Spirits is recalling 3,876 bottles of Cinnamon Infused Simple Syrup due to manufacturing in an unlicensed, uninspected facility with potential under-processing concerns.

    Product
    Cinnamon Infused Simple Syrup is a non-alcoholic cocktail mixer. Product is packaged in glass 5oz. bottle and sold under brand Urban River Spirits.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-1624-2024·2024-08-14

    Non-alcoholic cocktail mixer recalled due to facility and processing concerns

    Urban River Spirits recalls Tropical Blackberry cocktail mixer (3,876 bottles) due to manufacturing in an unlicensed, uninspected facility with potential under-processing. No illnesses reported.

    Product
    Tropical Blackberry is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-1627-2024·2024-08-14

    Non-Alcoholic Cocktail Mixer Recalled Due to Facility Safety Concerns

    Cafe Caramel Delight, a non-alcoholic cocktail mixer, is being recalled because it was produced in an unlicensed, uninspected facility with potential under-processing concerns.

    Product
    Cafe Caramel Delight is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Drugs)·D-0627-2024·2024-08-14

    Acetaminophen 500mg Rapid Release Gelcaps Recalled for Carton Label Mix-up

    Walgreen Co. is recalling Acetaminophen 500mg Rapid Release Gelcaps (Lot #31670346AA, expires 12/31/2026) due to incorrect carton labeling. The 21,192 affected bottles were distributed to retailers in Illinois.

    Product
    Acetaminophen, USP 500mg, Pain Reliever/Fever Reducer, Extra Strength, Rapid Release Gelcaps, packaged in a 225-count HDPE bottle, further packaged in a carton, Distributed by Walgreen Co., 200 Wilmot Rd, Deerfield, IL 60015, Made in India
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1622-2024·2024-08-14

    Pear-Tini Mixer recalled due to production in unlicensed facility

    Urban River Spirits is recalling Pear-Tini Mixer because it was made in an unlicensed and uninspected facility. The product may not have been properly processed.

    Product
    Pear-Tini Mixer is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Drugs)·D-0629-2024·2024-08-14

    Methotrexate tablets may contain wrong medication, FDA says

    Amneal Pharmaceuticals recalls Methotrexate 2.5mg tablets (Lot BB29124) distributed nationwide due to potential presence of Fludrocortisone Acetate tablets. Patients should verify their lot number with their pharmacy.

    Product
    Methotrexate Tablets, USP, 2.5mg, 100-count Bottle, RX Only, Distributed By: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC# 69238-1423-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1621-2024·2024-08-14

    Non-Alcoholic Cocktail Mixer Recalled for Potential Under-Processing Issue

    Urban River Spirits is recalling 3876 bottles of Blackberry and Lime Mixer manufactured in an unlicensed, uninspected facility with potential under-processing. Consumers across 11 states should not consume the product.

    Product
    Blackberry and Lime Mixer is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-2505-2024·2024-08-14

    Surgical Laser System Recalled Due to Wireless Footswitch Pairing Difficulties

    Olympus Corporation is recalling the Soltive Pro SuperPulsed Laser System due to difficulties pairing its wireless footswitch, which could delay surgical procedures. The recall affects 253 units worldwide.

    Product
    Soltive Pro SuperPulsed Laser System, Model TFL-SLS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1636-2024·2024-08-14

    Vanilla Infused Simple Syrup Recalled Over Potential Under-Processing Risk

    Urban River Spirits Vanilla Infused Simple Syrup is being recalled. The product was made in an unlicensed and uninspected facility with potential under-processing, raising food safety concerns.

    Product
    Vanilla Infused Simple Syrup is a non-alcoholic cocktail mixer. Product is packaged in glass 5oz. bottle and sold under brand Urban River Spirits.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-1618-2024·2024-08-14

    Non-Alcoholic Cocktail Mixer Recalled for Facility Safety and Under-Processing Concerns

    Urban River Spirits is recalling 3,876 bottles of Spicy Cool-aid: Watermelon & Jalapeno due to potential under-processing. The product was manufactured in an unlicensed and uninspected facility.

    Product
    Spicy Cool-aid: Watermelon & Jalapeno is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-1634-2024·2024-08-14

    Urban River Spirits Cocktail Mixer Recalled for Potential Under-Processing

    Urban River Spirits Crisp Cucumber and Mint cocktail mixer recalled due to production in an unlicensed, uninspected facility. Potential under-processing poses a safety risk.

    Product
    Crisp Cucumber and Mint is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-1625-2024·2024-08-14

    Non-Alcoholic Cocktail Mixer from Urban River Spirits Recalled for Potential Under-Processing

    Urban River Spirits is recalling Peppered Peach Bliss, a non-alcoholic cocktail mixer, due to potential under-processing risks. The product was manufactured in an unlicensed and uninspected facility.

    Product
    Peppered Peach Bliss is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-1619-2024·2024-08-14

    Urban River Spirits Grapefruit Mixer Recalled for Potential Under-Processing

    Urban River Spirits is recalling Ruby-Red Grapefruit Mixer due to potential under-processing of the non-alcoholic beverage made in an unlicensed facility. No illnesses have been reported.

    Product
    Ruby-Red Grapefruit Mixer is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-1652-2024·2024-08-14

    Frozen Cornbread Muffins Recalled Due to Manufacturing and Sanitation Violations

    Frozen Food Processors recalls frozen cornbread muffins manufactured without state license and in unsanitary conditions. The recall affects approximately 1,862 cases distributed in MS, TN, LA, AR, and AL.

    Product
    Frozen Food Processors - Regular Cornbread Muffins packaged in 2oz corrugated cardboard boxes lined with food grade plastic bags. Keep frozen at 0F or lower until time of use. 96 individual muffins per case.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-1653-2024·2024-08-14

    Frozen Jalapeno Cornbread Muffins Recalled for Unsanitary Manufacturing

    Frozen Food Processors recalls Jalapeno Cornbread Muffins due to manufacturing without state license and in unsanitary conditions. 259 cases were distributed to five states.

    Product
    Frozen Food Processors - Jalapeno Cornbread Muffins packaged in 2oz corrugated cardboard boxes lined with food grade plastic bags. Keep frozen at 0F or lower until time of use. 96 individual muffins per case.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-1628-2024·2024-08-14

    Non-Alcoholic Cocktail Mixer Recalled Due to Potential Under-Processing in Unlicensed Facility

    Urban River Spirits' Spicy Orange and Mango Fusion non-alcoholic cocktail mixer is recalled due to production in an unlicensed, uninspected facility with potential under-processing. Approximately 3,876 bottles were distributed across 11 states.

    Product
    Spicy Orange and Mango Fusion is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-1626-2024·2024-08-14

    Non-alcoholic cocktail mixer recalled for potential under-processing

    Urban River Spirits is recalling Lush Lavender & Wildberry Spritz non-alcoholic mixer due to potential under-processing. The product was manufactured in an unlicensed and uninspected facility.

    Product
    Lush Lavender & Wildberry Spritz is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    11 states
  • LowFDA (Devices)·Z-2535-2024·2024-08-14

    NavaClick Syringe and Needle Model LIN02 Recalled for Incorrect Carton GTIN Label

    Lineage Biomedical is recalling NavaClick Syringe and Needle Model LIN02 due to an incorrect GTIN number on carton packaging. The recall affects 215 cartons distributed in Michigan and South Carolina.

    Product
    NavaClick Syringe and Needle, Model Number LIN02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0625-2024·2024-08-14

    Sevelamer Carbonate for Oral Suspension missing lot and expiration date labels

    Dr. Reddy's Laboratories is recalling Sevelamer Carbonate for Oral Suspension packets missing lot number and expiration date information. Approximately 5,136 cartons were distributed nationwide.

    Product
    SEVELAMER CARBONATE FOR ORAL SUSPENSION — SEVELAMER CARBONATE FOR ORAL SUSPENSION (SEVELAMER CARBONATE FOR ORAL SUSPENSION)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V608000·2024-08-13

    BMW Recalls Multiple Models Due to Water Pump Electrical Fire Risk

    BMW is recalling 720,796 vehicles from 2012-2018 because an improperly sealed water pump connector may short circuit, increasing the risk of a fire.

    Product
    BMW — BMW X4, 328I, 228XI, Z4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V606000·2024-08-13

    Cruiser Stryker Travel Trailers Recalled for Generator Venting Defect

    Cruiser RV is recalling 2024-2025 Stryker travel trailers with optional Onan 5.5 generators due to improper venting that may cause overheating or trapped exhaust.

    Product
    CRUISER — CRUISER STRYKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V607000·2024-08-13

    Motorhome Overhead Cabinet Fasteners May Break and Cause Detachment

    Motorhomes with HappiJac drop-down beds have front overhead cabinet fasteners that can break and detach while in motion. This can distract drivers and increase crash risk.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER FLAIR, STORM, ADMIRAL XE, PACE ARROW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V599000·2024-08-12

    Blue Bird Recalls 2018-2021 Vision School Buses for Fuel Line Defect

    Blue Bird is recalling 2018-2021 Vision school buses with 6.8L gasoline engines because improperly applied fuel line coating may cause leaks and fire risk.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V600000·2024-08-12

    Blue Bird Recalls 2018-2021 Vision Transit Buses for Fuel Line Defect

    Blue Bird is recalling 2018-2021 Vision transit buses with 6.8L gasoline engines because improperly applied fuel line coating may cause leaks and fire risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V602000·2024-08-12

    Motiv Recalls 2020-2023 Electric School Buses for Software Defect

    Motiv Power Systems is recalling 2020-2023 electric school buses because a software error could shut down high-voltage batteries, causing a loss of steering and brake power assist.

    Product
    MOTIV — MOTIV E-450 BEV CHASSIS SCHOOL BUS, F-59 BEV CHASSIS SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V603000·2024-08-12

    Motiv Recalls 2021-2023 E-450 School Buses Due to Wiring Defect

    Motiv Power Systems is recalling 2021-2023 E-450 school buses because damaged CAN signal wires could cause a loss of drive power, increasing crash risk.

    Product
    MOTIV — MOTIV E-450 BEV CHASSIS SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V593000·2024-08-09

    2024 Ford Mustang Rear Suspension Knuckle Casting Defect Recall

    Ford is recalling certain 2024 Mustang vehicles because the rear suspension knuckles may have a casting defect that causes loss of handling and steering control, increasing crash risk.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V598000·2024-08-09

    2020-2022 Ford Explorer Engine Compartment Fire Risk Recall

    Certain 2020-2022 Ford Explorers may experience engine failures that release oil and fuel vapors, risking engine compartment fires. Ford will update the engine control software and inspect for bearing damage.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E067000·2024-08-09

    Cruise Recalls 1,194 Autonomous Vehicles for Software Braking Defect

    Cruise LLC is recalling 1,194 autonomous vehicles due to a software defect that may cause unexpected braking when vehicles or cyclists approach from behind.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V597000·2024-08-09

    2024 Ford Ranger Power Windows May Not Reverse When Detecting Objects

    Ford is recalling 2024 Ranger vehicles because power windows may fail to automatically reverse when detecting an object, risking pinching injuries to occupants.

    Product
    FORD — FORD, LINCOLN RANGER, NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V594000·2024-08-09

    Ford windshield wiper motor failure recall affects Mach-E and other models

    Ford is recalling certain 2023–2024 Mustang Mach-E, Maverick, and Bronco Sport vehicles because the windshield wiper motor may become inoperative, reducing visibility and increasing crash risk. Dealers will replace the motor free of charge.

    Product
    FORD — FORD BRONCO SPORT, MAVERICK, MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V590000·2024-08-09

    2022 Ford Maverick Electrical System Defect Increases Crash Risk

    Ford is recalling certain 2022 Mavericks due to a defect in body and power train control modules that may fail to detect changes in 12-volt battery charge, potentially resulting in loss of hazard lights or drive power and increasing the risk of crashes.

    Product
    FORD — FORD MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E066000·2024-08-08

    GM Recalls Buick Envision All-Weather Floor Mats Due to Pedal Trap Risk

    General Motors is recalling 2024 Buick Envision vehicles with specific all-weather floor mats because the accelerator pedal may become trapped, increasing crash risk.

    Product
    BUICK — BUICK ALL-WEATHER FLOOR LINER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V587000·2024-08-08

    Toyota Recalls 2025 Lexus UX300h for Wire Harness Defect

    Toyota is recalling 2025 Lexus UX300h vehicles because a wire harness defect may cause a loss of drive power, increasing the risk of a crash.

    Product
    LEXUS — LEXUS UX HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V588000·2024-08-08

    BMW Recalls 2018 540D xDrive Vehicles for Engine Fire Risk

    BMW is recalling 2018 540D xDrive vehicles previously repaired under recall 22V-614 because the EGR cooler may leak, causing coolant to mix with soot and increasing the risk of an engine fire.

    Product
    BMW — BMW 540D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24335·2024-08-08

    Samsung Slide-In Electric Ranges Recalled Due to Fire Hazard

    Samsung is recalling about 1.12 million slide-in electric ranges because front-mounted knobs can be accidentally activated by humans or pets, causing fires and injuries. Samsung will provide free knob locks or covers.

    Product
    Slide-in Electric Ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V586000·2024-08-08

    2024 Jeep Grand Cherokee child seat tether welds may be insufficient

    Chrysler is recalling certain 2024 Jeep Grand Cherokee L vehicles because child seat tether welds may be insufficient, reducing restraint during crashes. Dealers will reinforce the welds at no charge.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V589000·2024-08-08

    2023-2024 Cadillac LYRIQ recalled for brake control defect

    General Motors is recalling 2023-2024 Cadillac LYRIQ all-wheel drive vehicles because the anti-lock brake system may activate unexpectedly and release brake pressure, potentially causing loss of braking ability.

    Product
    CADILLAC — CADILLAC LYRIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V585000·2024-08-08

    2024 Jeep Wrangler Recalled for Obstructed Tail Lights

    Chrysler is recalling 2024 Jeep Wrangler vehicles because incorrect tail lights may be obstructed by the spare tire, reducing visibility to other drivers.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·24334·2024-08-08

    SMEG Refrigerators Recalled Due to Detachable Door Injury Hazard

    SMEG USA is recalling about 900 SMEG-branded retro refrigerators because the door can detach and fall off, posing an injury hazard. The firm has received nine reports of doors falling off but no injuries have been reported.

    Product
    SMEG Refrigerators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24337·2024-08-08

    Finger-Ease Guitar String Lubricants Recalled Due to Skin Irritation Risk

    Chem-Pak is recalling Finger-Ease Guitar String Lubricants because one production batch contains a contaminant that poses a risk of skin irritation. One report of minor skin irritation has been received.

    Product
    Finger-Ease Guitar String Lubricants
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1535-2024·2024-08-07

    Diamond Shruumz Gummies Recalled for Toxic Levels of Muscimol

    Diamond Shruumz Gummies (Micro Dose Sour Peach Apple) manufactured by Prophet Premium Blends, LLC, are being recalled by the FDA due to toxic levels of muscimol. The Class I recall affects approximately 248,007 products distributed nationwide.

    Product
    Diamond Shruumz Gummies - Micro Dose Sour Peach Apple UPC 755003861386
    Category
    Food
    Distribution
    51 states
  • CriticalFDA (Drugs)·D-0620-2024·2024-08-07

    Dietary Supplement Recalled for Undeclared Diclofenac and Omeprazole

    SoloVital's Umary Hyaluronic Acid supplement was recalled because FDA testing found it contains undeclared Diclofenac and Omeprazole. The product, marketed without approved NDA/ANDA, affected 1,331 bottles distributed nationwide.

    Product
    Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count bottles.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1540-2024·2024-08-07

    Diamond Shruumz Gummies recalled for toxic muscimol levels

    Diamond Shruumz Gummies Mega/Extreme Dose Peach Paradise contain toxic levels of muscimol. The FDA is recalling all 248,007 units distributed nationwide.

    Product
    Diamond Shruumz Gummies - Mega/Extreme Dose Peach Paradise UPC 810133320384
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1523-2024·2024-08-07

    Diamond Shruumz Cones Sprinkles Recalled for Toxic Muscimol Levels

    Prophet Premium Blends, LLC is recalling Diamond Shruumz Infused Cones Sprinkles due to toxic levels of muscimol. The recall affects approximately 248,007 products distributed nationwide.

    Product
    Diamond Shruumz Infused Cones Sprinkles UPC 810133320063
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1532-2024·2024-08-07

    Diamond Shruumz Gummies Recalled for Toxic Muscimol Levels

    Diamond Shruumz Gummies - Micro Dose Blue Raz Watermelon are being recalled nationwide due to toxic levels of muscimol. All lots are affected.

    Product
    Diamond Shruumz Gummies - Micro Dose Blue Raz Watermelon UPC 755003861362
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1545-2024·2024-08-07

    Friendly's Celebration Ice Cream Cake Recalled Due to Listeria Contamination Risk

    Friendly's Celebration Ice Cream Cake is being recalled due to possible Listeria monocytogenes contamination. Consumers should discard or return affected products.

    Product
    Friendly's Celebration Ice Cream Cake 60 fl oz, UPC 29839000920. Packaged in cardboard box, 4 boxes per case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1522-2024·2024-08-07

    Diamond Shruumz Infused Cones Recalled for Toxic Muscimol Levels

    Diamond Shruumz Infused Cones Double Chocolate Chip are recalled due to toxic levels of muscimol. Approximately 248,007 units were distributed nationwide and should not be consumed.

    Product
    Diamond Shruumz Infused Cones Double Chocolate Chip UPC 810133320001
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1524-2024·2024-08-07

    Diamond Shruumz Infused Cones Recalled for Toxic Levels of Muscimol

    Diamond Shruumz Infused Cones Mint Chocolate Chip are recalled due to toxic levels of muscimol. The product was distributed nationwide.

    Product
    Diamond Shruumz Infused Cones Mint Chocolate Chip UPC 810133320049
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1521-2024·2024-08-07

    Diamond Shruumz Infused Cones Recalled for Toxic Muscimol Levels

    Diamond Shruumz Infused Cones Cookies and Cream are being recalled due to toxic levels of muscimol. The FDA Class I recall affects approximately 248,007 units distributed nationwide.

    Product
    Diamond Shruumz Infused Cones Cookies and Cream UPC 810133320025
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1541-2024·2024-08-07

    Diamond Shruumz Gummies Recalled for Toxic Levels of Muscimol

    Diamond Shruumz Gummies are being recalled due to toxic levels of muscimol. The FDA Class I recall affects approximately 248,007 units distributed nationwide.

    Product
    Diamond Shruumz Gummies - Mega/Extreme Dose Radical Rainbow UPC 810133320407
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1528-2024·2024-08-07

    Diamond Shruumz Chocolate Bars Cinnamon Bar Recalled for Toxic Muscimol Levels

    Prophet Premium Blends is recalling Diamond Shruumz Chocolate Bars Cinnamon Bar products nationwide due to toxic levels of muscimol. Approximately 248,007 units were affected.

    Product
    Diamond Shruumz Chocolate Bars Cinnamon Bar UPC 755003858836
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1537-2024·2024-08-07

    Diamond Shruumz Micro Dose Gummies recalled for toxic muscimol levels

    Prophet Premium Blends is recalling Diamond Shruumz Gummies - Micro Dose Strawberry Kiwi nationwide because the product contains toxic levels of muscimol.

    Product
    Diamond Shruumz Gummies - Micro Dose Strawberry Kiwi UPC 755003861409
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Drugs)·D-0622-2024·2024-08-07

    Clonazepam Tablets Recalled Due to Carton Labeling Error

    Endo Pharmaceuticals is recalling 8,139 cartons of Clonazepam Orally Disintegrating Tablets due to carton labeling errors. The carton labels incorrectly state 0.125 mg while the actual tablets inside contain 0.25 mg.

    Product
    CLONAZEPAM — CLONAZEPAM (CLONAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1533-2024·2024-08-07

    Diamond Shruumz Grape Lemonade Gummies recalled for toxic muscimol levels

    Diamond Shruumz Gummies - Micro Dose Grape Lemonade (UPC 755003861584) are being recalled by the FDA due to toxic levels of muscimol. The product was distributed across all U.S. states, affecting approximately 248,007 units.

    Product
    Diamond Shruumz Gummies - Micro Dose Grape Lemonade UPC 755003861584
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1526-2024·2024-08-07

    Diamond Shruumz Chocolate Bars Recalled for Toxic Muscimol Contamination

    Diamond Shruumz Chocolate Bars Cookies & Cream are being recalled due to toxic levels of muscimol. The FDA Class I recall affects approximately 248,007 products distributed nationwide.

    Product
    Diamond Shruumz Chocolate Bars Cookies & Cream UPC 755003858782
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1536-2024·2024-08-07

    Diamond Shruumz Gummies Micro Dose Rainbow Recalled for Toxic Muscimol Levels

    Prophet Premium Blends is recalling Diamond Shruumz Gummies Micro Dose Rainbow nationwide due to toxic levels of muscimol. The FDA classified this as a Class I recall.

    Product
    Diamond Shruumz Gummies - Micro Dose Rainbow UPC 755003861614
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1539-2024·2024-08-07

    Diamond Shruumz Lemon Lime Gummies Recalled for Toxic Muscimol

    Diamond Shruumz Gummies are recalled nationwide due to toxic levels of muscimol contamination. All lots are affected, totaling 248,007 units.

    Product
    Diamond Shruumz Gummies - Mega/Extreme Dose Lucid Lemon Lime UPC 810133320360
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Drugs)·D-0619-2024·2024-08-07

    Potassium Chloride Extended-Release Capsules Recalled Over Failed Dissolution

    Amerisource Health Services LLC is recalling 61,231 bottles of Potassium Chloride Extended-Release Capsules nationwide due to failed dissolution specifications. The medication may not release properly, potentially affecting dosing accuracy.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1542-2024·2024-08-07

    Diamond Shruumz Gummies recalled for toxic muscimol levels

    FDA recalls Diamond Shruumz Gummies Watermelon Wonderland (UPC 810133320421) due to toxic levels of muscimol. Approximately 248,007 units distributed across the United States are affected.

    Product
    Diamond Shruumz Gummies - Mega/Extreme Dose Watermelon Wonderland UPC 810133320421
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1538-2024·2024-08-07

    Diamond Shruumz Gummies Blue Razz recalled for toxic muscimol levels

    Prophet Premium Blends is recalling Diamond Shruumz Gummies Blue Razz containing toxic levels of muscimol. The product has been distributed nationwide across all U.S. states and territories.

    Product
    Diamond Shruumz Gummies - Mega/Extreme Dose Blue Razz Euphoria UPC 810133320346
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1525-2024·2024-08-07

    Diamond Shruumz Infused Cones Recalled for Toxic Muscimol Levels

    Diamond Shruumz Infused Cones Strawberry Cheesecake are recalled due to toxic levels of muscimol. The FDA Class I recall affects approximately 248,007 units distributed nationwide.

    Product
    Diamond Shruumz Infused Cones Strawberry Cheesecake UPC 810133320087
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1529-2024·2024-08-07

    Diamond Shruumz Chocolate Bars Recalled for Toxic Muscimol Levels

    Prophet Premium Blends is recalling Diamond Shruumz Chocolate Bars Birthday Cake due to toxic levels of muscimol. The recall affects 248,007 products distributed nationwide.

    Product
    Diamond Shruumz Chocolate Bars Birthday Cake UPC 75503858867
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1527-2024·2024-08-07

    Diamond Shruumz Chocolate Bars Recalled for Toxic Muscimol Levels

    Diamond Shruumz Chocolate Bars Cookie Butter are recalled due to toxic levels of muscimol. The product was distributed nationwide to all U.S. states and Puerto Rico.

    Product
    Diamond Shruumz Chocolate Bars Cookie Butter UPC 755003858751
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1534-2024·2024-08-07

    Diamond Shruumz Gummies Recalled for Toxic Muscimol Levels Nationwide

    Prophet Premium Blends is recalling Diamond Shruumz Gummies (Micro Dose Hawaiian Punch) due to toxic levels of muscimol. The recall affects 248,007 units distributed nationwide.

    Product
    Diamond Shruumz Gummies - Micro Dose Hawaiian Punch UPC 755003861850
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1531-2024·2024-08-07

    Diamond Shruumz Chocolate Bars Recalled Due to Toxic Muscimol Levels

    Prophet Premium Blends is recalling Diamond Shruumz Chocolate Bars Fruity Cereal due to toxic levels of muscimol contamination. Products have been distributed nationwide across the United States.

    Product
    Diamond Shruumz Chocolate Bars Fruity Cereal UPC 755003858799
    Category
    Food
    Distribution
    51 states
  • SevereFDA (Food)·F-1530-2024·2024-08-07

    Diamond Shruumz Chocolate Bars recalled for toxic muscimol contamination

    Prophet Premium Blends, LLC is recalling Diamond Shruumz Chocolate Bars Dark Chocolate due to toxic levels of muscimol. All lots distributed nationwide should not be consumed.

    Product
    Diamond Shruumz Chocolate Bars Dark Chocolate UPC 755003858829
    Category
    Food
    Distribution
    51 states
  • HighFDA (Food)·F-1608-2024·2024-08-07

    Dolcezza Peanut Butter Stracciatella Gelato Recalled for Possible Listeria Contamination

    Dolcezza Peanut Butter Stracciatella Gelato is being recalled due to possible contamination with Listeria monocytogenes. The recall affects 2,355 cases distributed nationwide with best-by dates between May 20, 2024 and June 20, 2025.

    Product
    Dolcezza Peanut Butter Stracciatella Gelato 16 fl oz/1 pint, UPC 857838006090. Packaged in paper containers, 8 containers per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1570-2024·2024-08-07

    Chipwich Ice Cream Sandwich Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling Chipwich Double Chocolate Chip Ice Cream Sandwiches due to possible Listeria monocytogenes contamination. The recall affects 6,722 cases distributed nationwide with best-by dates from February 23, 2025 to December 21, 2025.

    Product
    Chipwich Double Chocolate Chip Ice Cream Sandwich 4 fl oz, UPC 810493030329. Individually plastic wrapped sandwiches packaged in a carboard box. 12 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1583-2024·2024-08-07

    LaSalle Butter Pecan Ice Cream recalled for possible Listeria contamination

    Totally Cool, Inc. is recalling LaSalle Butter Pecan Ice Cream nationwide due to possible Listeria monocytogenes contamination. Affected consumers should return or discard the product.

    Product
    LaSalle Butter Pecan Ice Cream 16 fl oz/1 pint, UPC 671891374091. Packaged in paper containers, 8 containers per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1550-2024·2024-08-07

    Hershey's Ice Cream Cake Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling Hershey's Ice Cream Vanilla & Chocolate Flavored Ice Cream Cake due to possible Listeria monocytogenes contamination. The recall affects 16,027 cases distributed nationwide.

    Product
    Hershey s Ice Cream Vanilla & Chocolate Flavored Ice Cream Cake 38 fl oz 7", UPC 24682060008. Packaged in cardboard box, 4 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1563-2024·2024-08-07

    Jeni's Ice Cream Sandwiches Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling Jeni's Ice Cream Sandwiches Triple Berry Tart due to possible Listeria monocytogenes contamination. The affected products were distributed nationwide.

    Product
    Jeni's Ice Cream Sandwiches Triple Berry Tart 3.5 fl oz UPC 858241006851. Individually wrapped in plastic and packaged in cardboard box, 3 sandwiches per box. 8 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1564-2024·2024-08-07

    Hershey's Ice Cream Cones Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling 197,701 cases of Hershey's Ice Cream Cookies and Cream Cones due to possible Listeria monocytogenes contamination. Affected codes 3174–4047 were distributed nationwide.

    Product
    Hershey's Ice Cream Cookies and Cream Ice Cream Cone 4 fl oz UPC 24682313067. Individually packaged in paper. 3 sandwiches per box. 24 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1586-2024·2024-08-07

    LaSalle Dulce De Leche Ice Cream Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling LaSalle Dulce De Leche Ice Cream due to possible Listeria monocytogenes contamination. The recall affects 6,043 cases distributed nationwide.

    Product
    LaSalle Dulce De Leche Ice Cream 16 fl oz/1 pint, UPC 671891374152. Packaged in paper containers, 8 containers per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2457-2024·2024-08-07

    Arctic Sun Temperature Management System software failure may disable critical safety alarms

    Arctic Sun Temperature Management Systems may fail to reach target temperature and critically fail to alert clinicians. The software defect affects approximately 10,507 units worldwide and risks hypothermia or hyperthermia.

    Product
    Arctic Sun Temperature Management Systems, Name/REF: Arctic Sun STAT, NA/6000-00-00; Arctic Sun STAT Loaner, NA/6000-00-00L; Arctic Sun Stat EU UK/600001; Arctic Sun Stat Taiwan/600006; Arctic Sun Stat Japan/600020; Arctic Sun 5000, NA/5000-00-00; Arctic Sun 5000, NA w/ T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1593-2024·2024-08-07

    Marco Dulce De Leche & Cookies Ice Cream recalled for possible Listeria contamination

    Totally Cool, Inc. is recalling Marco Dulce De Leche & Cookies Ice Cream due to possible Listeria monocytogenes contamination. Approximately 17,633 cases were distributed nationwide.

    Product
    Marco Dulce De Leche & Cookies Ice Cream 16 fl oz/1 pint, UPC 860006880514. Packaged in paper containers, 8 containers per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1599-2024·2024-08-07

    Dolcezza Sugar Cookie Dough Gelato recalled for possible Listeria contamination

    Totally Cool, Inc. is recalling Dolcezza Sugar Cookie Dough Gelato due to possible contamination with Listeria monocytogenes. Consumers should not consume the product and should discard it or return it to the retailer.

    Product
    Dolcezza Sugar Cookie Dough Gelato 16 fl oz/1 pint, UPC 857838006618. Packaged in paper containers, 8 containers per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1554-2024·2024-08-07

    Yelloh! Ice Cream Sandwiches Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling Yelloh! Chocolate Chip Ice Cream Sandwiches nationwide for possible Listeria monocytogenes contamination. Do not consume; dispose of or return the product (codes 6T3115–6T4171).

    Product
    Yelloh! Chocolate Chip Ice Cream Sandwich With Vanilla Ice Cream 24 fl oz UPC 810038685106. Individually wrapped in plastic. 6 sandwiches packaged in cardboard box, 12 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1601-2024·2024-08-07

    Dolcezza Dark Chocolate Fudge Gelato recalled for possible Listeria contamination

    Dolcezza Dark Chocolate Fudge Gelato 16 fl oz containers distributed nationwide are being recalled due to possible contamination with Listeria monocytogenes. No illnesses have been reported.

    Product
    Dolcezza Dark Chocolate Fudge Gelato 16 fl oz/1 pint, UPC 857838006014. Packaged in paper containers, 8 containers per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1575-2024·2024-08-07

    Frozen Farms Watermelon Sorbet Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling The Frozen Farms Farm Crafted Watermelon Sorbet for possible Listeria monocytogenes contamination. Affected products were distributed nationwide with Best by Dates between 09/05/25 and 07/30/26.

    Product
    The Frozen Farms Farm Crafted Watermelon Sorbet 16 fl oz/1 pint, UPC 850023398024. Packaged in paper containers, 8 containers per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1603-2024·2024-08-07

    Dolcezza Dark Chocolate Gelato Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling Dolcezza Dark Chocolate Gelato due to possible Listeria monocytogenes contamination. Affected products have Best By dates between May 20, 2024 and June 20, 2025.

    Product
    Dolcezza Dark Chocolate Gelato 16 fl oz/1 pint, UPC 857838006083. Packaged in paper containers, 8 containers per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1547-2024·2024-08-07

    Frozen ice cream cake recalled for possible Listeria contamination

    Totally Cool, Inc. is recalling Abilyn's Frozen Bakery Ice Cream Cake due to possible Listeria monocytogenes contamination. The recall affects 12,586 cases distributed nationwide.

    Product
    Abilyn s Frozen Bakery Ice Cream Cake Vanilla & Chocolate 6", UPC 851545008002. Packaged in cardboard box, 3 boxes per case. Abilyn s Frozen Bakery Ice Cream Cake Vanilla & Chocolate 8", UPC 851545008019. Packaged in cardboard box, 2 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1543-2024·2024-08-07

    Hill Country Fare Mustard Potato Salad recalled due to plastic contamination

    Reser's Fine Foods is recalling Hill Country Fare Mustard Potato Salad because some containers may contain plastic foreign material. Consumers in Texas should not consume this product.

    Product
    Hill Country Fare Mustard Potato Salad refrigerated product is packaged in clear square plastic container with printed white plastic lid, net 48oz (3lb) 1.36 KG. UPC 4122003165. Distributed by H-E-B, San Antonio, TX 78204. There are 6 containers per case.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1551-2024·2024-08-07

    Hershey's ice cream sheet cake recalled for possible Listeria contamination

    Totally Cool, Inc. is recalling Hershey's ice cream sheet cake due to possible contamination with Listeria monocytogenes. The FDA Class II recall affects 14,180 cases distributed nationwide.

    Product
    Hershey s Ice Cream Vanilla & Chocolate Flavored Ice Cream Sheet Cake 110 fl oz, UPC 24682060152. Packaged in cardboard box, 3 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1610-2024·2024-08-07

    Dolcezza Swiss Chocolate ice cream recalled due to possible Listeria contamination

    Totally Cool, Inc. is recalling Dolcezza Swiss Chocolate ice cream (16 oz) due to possible Listeria monocytogenes contamination. The 6,338 cases affected were distributed nationwide.

    Product
    Dolcezza Swiss Chocolate 16 fl oz/1 pint, UPC 857838006342. Packaged in paper containers, 8 containers per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1549-2024·2024-08-07

    Abilyn's Frozen Ice Cream Cake Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling Abilyn's Frozen Bakery Ice Cream Cake 'For the Love of Chocolate' due to possible Listeria monocytogenes contamination. The recall affects approximately 2,993 cases distributed nationwide with best-by dates from May 20, 2024 through May 28, 2025.

    Product
    Abilyn s Frozen Bakery Ice Cream Cake For the Love of Chocolate 6", UPC 851545008057. Packaged in cardboard box, 4 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide

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