The Recall Desk

Archive

August 2025 recalls

523 recalls were announced in August 2025.

What the numbers show

Critical
39
Severe
106
High
239
Moderate
138
Low
1

Of the 523 recalls this month scored against our rubric, 7% are Critical, 20% are Severe.

301–400 of 523

  • ModerateFDA (Food)·H-0418-2025·2025-08-13

    Yoplait strawberry banana yogurt recalled after a shipping trailer temperature excursion

    Yoplait Original Strawberry Banana Yogurt, 6 oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 2 units are affected.

    Product
    Yoplait Original Strawberry Banana Yogurt, 6 OZ (170g), packaged in a plastic cup, UPC: 170470003136
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2252-2025·2025-08-13

    HVI cardiac robot packs contain an inadvertently resterilized visualization system

    HVI Cardiac Robot Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 20 units are affected.

    Product
    HVI CARDIAC ROBOT PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2249-2025·2025-08-13

    GS endoscopy packs contain an inadvertently resterilized visualization system

    GS Endoscopy Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 816 units are affected.

    Product
    GS ENDOSCOPY PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0416-2025·2025-08-13

    Velveeta sharp cheddar slices recalled after a shipping trailer temperature excursion

    Velveeta Slices Sharp Cheddar, 16 count, are being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Velveeta Slices Sharp Cheddar, 16 ct., NET WT 12 OZ (340g), packaged in plastic/cardboard, UPC: 021000044894
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0401-2025·2025-08-13

    Clover Valley 2% reduced fat milk recalled after a temperature excursion

    Clover Valley 2% Reduced Fat Milk in gallon and half gallon jugs is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 13 units affected.

    Product
    1) Clover Valley 2% Reduced Fat Milk, 1 GAL (3.78 L), packaged in a plastic jug, UPC: 070744002202 2) Clover Valley 2% Reduced Fat Milk, 1/2 GAL (1.89 L), packaged in a plastic jug, UPC: 070744009652
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2244-2025·2025-08-13

    daVinci TruCustom bundles contain an inadvertently resterilized visualization system

    DAVINCI TRUCUSTOM BUNDLE medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 626 units are affected.

    Product
    DAVINCI TRUCUSTOM BUNDLE. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2245-2025·2025-08-13

    daVinci urology kits contain an inadvertently resterilized visualization system

    DAVINCI UROLOGY medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 166 units are affected.

    Product
    DAVINCI UROLOGY. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0411-2025·2025-08-13

    Shamrock Farms protein shakes recalled after a shipping trailer temperature excursion

    Shamrock Farms Chocolate Rockin' Protein Builder Protein Shake, 12 fl oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 2 units affected.

    Product
    Shamrock Farms Chocolate Rockin' Protein Builder Protein Shake, 12 FL OZ (354 ML), packaged in a plastic bottle, UPC: 028300004054
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2259-2025·2025-08-13

    General robotic packs contain an inadvertently resterilized visualization system

    PACK GENERAL ROBOTIC medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 656 units are affected.

    Product
    PACK GENERAL ROBOTIC. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2238-2025·2025-08-13

    BD Trucount control kits carry incorrect standard deviation values for beads

    BD Trucount Controls 30 Test kits are being recalled because they contain incorrect standard deviation values for the low and high control beads, which compromises accurate bead count calculation. 629 kits affected.

    Product
    BD Trucount Controls, 30 Test - REF: 340335
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2254-2025·2025-08-13

    Laparoscopic GYN kits contain an inadvertently resterilized visualization system

    Laparoscopic GYN medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 18 units are affected.

    Product
    LAPAROSCOPIC GYN. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2269-2025·2025-08-13

    UniCel DxI 600 analyzer motor current resets below the required setting

    UniCel DxI 600 Access Immunoassay Analyzers are being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors. 271 systems are affected.

    Product
    UniCel DxI 600 Access Immunoassay Analyzer, Part Number A30260
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2243-2025·2025-08-13

    daVinci urology and prostate packs contain a resterilized visualization system

    DA VINCI PACK URO/PROSTATE medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 21 units affected.

    Product
    DA VINCI PACK URO/PROSTATE. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0404-2025·2025-08-13

    Imperial vegetable oil spread recalled after a shipping trailer temperature excursion

    Imperial 48% Vegetable Oil Spread Margarine Sticks are being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 8 units are affected.

    Product
    Imperial 48% Vegetable Oil Spread Margarine Sticks, NET WT 16 OZ (1 LB) 453g, packaged in a cardboard box, UPC: 011115871324
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2237-2025·2025-08-13

    BD Trucount 664343 control kits carry incorrect standard deviation values

    BD Trucount Controls 30 Test kits, REF 664343, are being recalled because they contain incorrect standard deviation values for the low and high control beads. 10 kits are affected.

    Product
    BD Trucount Controls, 30 Test - REF: 664343, RxOnly, IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0395-2025·2025-08-13

    Checkers famous seasoned fries recalled after a temperature excursion

    Checkers Famous Seasoned Fries, 28 oz, are being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Checkers Famous Seasoned Fries, NET WT 28 OZ (1 LB 12 OZ) 793g, packaged in a plastic/vinyl bag, UPC: 043301305818
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0396-2025·2025-08-13

    Chobani Flip cookie dough yogurt recalled after a temperature excursion

    Chobani Flip Cookie Dough Greek Yogurt, 4.5 oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Chobani Flip Cookie Dough Greek Yogurt, NET WT. 4.5 OZ (128g), packaged in a plastic cup, UPC: 818290016652
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2263-2025·2025-08-13

    Robotic uro/gyn packs contain an inadvertently resterilized visualization system

    Robotic Uro/Gyn Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 372 units are affected.

    Product
    ROBOTIC URO/GYN PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0398-2025·2025-08-13

    Clover Valley shredded parmesan recalled after a temperature excursion

    Clover Valley Shredded Parmesan Cheese, 6 oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Clover Valley Shredded Parmesan Cheese, NET WT 6 OZ (170g), packaged in a plastic bag, UPC: 071505950428
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0414-2025·2025-08-13

    Simply Orange juice recalled after a shipping trailer temperature excursion

    Simply Orange Pulp Free Orange Juice in 46 fl oz and 11.5 fl oz bottles is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 2 units affected.

    Product
    1) Simply Orange Pulp Free Orange Juice, 46 FL OZ (1.4 QT) 1.36 L, packaged in a plastic bottle, UPC: 025000136788 2) Simply Orange Pulp Free Orange Juice, 11.5 FL OZ (340 mL), packaged in a plastic bottle, UPC: 025000000249
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2241-2025·2025-08-13

    Cardiac robot packs contain an inadvertently resterilized visualization system

    Cardiac Robot Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 20 units are affected.

    Product
    CARDIAC ROBOT PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0406-2025·2025-08-13

    Milo's extra sweet tea recalled after a shipping trailer temperature excursion

    Milo's Extra Sweet Tea, 1 gallon, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 3 units are affected.

    Product
    Milo's Extra Sweet Tea, 128 FL OZ (1 GAL) 3.78 L, packaged in a plastic jug, UPC: 091475931982
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2270-2025·2025-08-13

    DxI 600 immunoassay analyzer motor current resets below the required setting

    A DxI 600 Access Immunoassay Analyzer is being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors that could delay patient results.

    Product
    DxI 600 Access Immunoassay Analyzer W/Dual Gantry, Part Number A71461
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2246-2025·2025-08-13

    General laparoscopy packs contain an inadvertently resterilized visualization system

    Gen Laparoscopy Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 321 units are affected.

    Product
    GEN LAPAROSCOPY PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2266-2025·2025-08-13

    UniCel DxI 800 analyzer motor current resets below the required setting

    UniCel DxI 800 Access Immunoassay Analyzers are being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors that could delay patient results. 2,203 systems affected.

    Product
    UniCel DxI 800 Access Immunoassay Analyzer, Part Number 973100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2258-2025·2025-08-13

    Major thoracoscopy basins contain an inadvertently resterilized visualization system

    Major Thoracoscopy Basin medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 128 units are affected.

    Product
    MAJOR THORACOSCOPY BASIN. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0403-2025·2025-08-13

    Clover Valley vitamin D whole milk recalled after a temperature excursion

    Clover Valley Vitamin D Whole Milk in gallon and half gallon jugs is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 43 units affected.

    Product
    1) Clover Valley Vitamin D Whole Milk, 1 GAL (3.78 L), packaged in a plastic jug, UPC: 070744002196 2) Clover Valley Vitamin D Whole Milk, 1/2 GAL (1.89 L), packaged in a plastic jug, UPC: 070744009645
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0573-2025·2025-08-13

    Recombinate antihemophilic factor vials exposed to temperatures outside labeled storage

    Recombinate [Antihemophilic Factor (Recombinant)] 5 mL vials are being recalled because of CGMP deviations: the product was exposed to temperatures outside its labeled storage requirements. 3 units affected.

    Product
    RECOMBINATE, [Antihemophilic Factor (Recombinant)], 5 mL vials, Rx Only, Takeda Pharmaceuticals USA, Cambridge, MA 02142, NDC: 00944-2843-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2261-2025·2025-08-13

    Partial nephrectomy packs contain an inadvertently resterilized visualization system

    Partial Nephrectomy Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 52 units are affected.

    Product
    PARTIAL NEPHRECTOMY PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Drugs)·D-0571-2025·2025-08-13

    Xolair auto-injectors exposed to temperatures outside labeled storage requirements

    Xolair (omalizumab injection) 150 mg/mL auto-injectors are being recalled because of CGMP deviations: the product was exposed to temperatures outside its labeled storage requirements. 6 units affected.

    Product
    XOLAIR — XOLAIR (OMALIZUMAB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2271-2025·2025-08-13

    DxI 600 with Spot B analyzer motor current resets below requirement

    DxI 600 Access Immunoassay Analyzers with Spot B are being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors. 177 systems are affected.

    Product
    DxI 600 Access Immunoassay Analyzer W/Spot B, Part Number A71460
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2267-2025·2025-08-13

    DxI 800 immunoassay analyzer motor current resets below the required setting

    A DxI 800 Access Immunoassay Analyzer is being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors that could delay patient results.

    Product
    DxI 800 Access Immunoassay Analyzer W/Dual Gantry, Part Number A71457
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2257-2025·2025-08-13

    LAVH packs contain an inadvertently resterilized visualization system

    LAVH Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 292 units are affected.

    Product
    LAVH PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0393-2025·2025-08-13

    Cesarina sesame seed cookies omit sesame from the contains statement

    Cesarina Sesame Seed Cookies, 16 oz, are being recalled because sesame is not listed in the Contains statement. 40 cases are affected.

    Product
    SESAME SEED COOKIES Cesarina Cookies, Net Weight. 16 oz. (454g), packaged in plastic clam shell containers, 12 packages per master case. Dry storage.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2265-2025·2025-08-13

    T4 Total ELISA kit box expiry exceeds the standards' shelf life

    T4 Total ELISA kits are being recalled because the expiration date on the kit box label and Certificate of Analysis exceeded the shelf life of the standards and control solutions by two months. 47 units affected.

    Product
    Brand Name: T4 Total ELISA Product Name: T4 Total ELISA Model/Catalog Number: EIA-4568 Product Description: T4 Total ELISA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0400-2025·2025-08-13

    Clover Valley chocolate milk recalled after a shipping trailer temperature excursion

    Clover Valley 1% Low Fat Chocolate Milk, half gallon, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Clover Valley 1% Low Fat Chocolate Milk, 1/2 GAL (1.89 L), packaged in a plastic jug, UPC: 070744009942
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2250-2025·2025-08-13

    GYN laparoscopy packs contain an inadvertently resterilized visualization system

    GYN Laparoscopy Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 346 units are affected.

    Product
    GYN LAPAROSCOPY PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2253-2025·2025-08-13

    Lap chole packs contain an inadvertently resterilized visualization system

    Lap Chole Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 85 units are affected.

    Product
    LAP CHOLE PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2268-2025·2025-08-13

    DxI 800 with Spot B analyzer motor current resets below requirement

    DxI 800 Access Immunoassay Analyzers with Spot B are being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors. 451 systems are affected.

    Product
    DxI 800 Access Immunoassay Analyzer W/Spot B, Part Number A71456
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2240-2025·2025-08-13

    Laparoscopic trays contain an inadvertently resterilized visualization system

    Laparoscopic Tray medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 40 units are affected.

    Product
    LAPAROSCOPIC TRAY. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2247-2025·2025-08-13

    General laparoscopy trays contain an inadvertently resterilized visualization system

    General Laparoscopy Tray medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 574 units are affected.

    Product
    GENERAL LAPAROSCOPY TRAY. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0415-2025·2025-08-13

    Twister fruit punch recalled after a shipping trailer temperature excursion

    Twister Fruit Punch, 59 fl oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 2 units are affected.

    Product
    Twister Fruit Punch, 59 FL OZ (1.84 QT) 1.75 L, packaged in a paper carton, UPC: 048500021231
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0407-2025·2025-08-13

    Milo's famous sweet tea recalled after a shipping trailer temperature excursion

    Milo's Famous Sweet Tea, 1 gallon, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 2 units are affected.

    Product
    Milo's Famous Sweet Tea, 128 FL OZ (1 GAL) 3.78 L, packaged in a plastic jug, UPC: 091475511009
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0409-2025·2025-08-13

    Minute Maid tropical punch recalled after a shipping trailer temperature excursion

    Minute Maid Tropical Punch, 59 fl oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 3 units are affected.

    Product
    Minute Maid Tropical Punch, 59 FL OZ (1.8 QT) 1.75 L, packaged in a paper carton, UPC: 025000047695
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0402-2025·2025-08-13

    Clover Valley lactose free milk recalled after a temperature excursion

    Clover Valley Lactose Free 2% Reduced Fat Milk, 64 fl oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Clover Valley Lactose Free 2% Reduced Fat Milk, 64 FL OZ (2 QTS) 1.89 L, packaged in a paper carton, UPC: 070744010085
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0410-2025·2025-08-13

    Pillsbury cinnamon rolls recalled after a shipping trailer temperature excursion

    Pillsbury Cinnamon Rolls with Original Icing, 8 count, are being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Pillsbury Cinnamon Rolls Original Icing, 8 ct., NET WT 12.4 OZ (351g), packaged in a cardboard and aluminum tube, UPC: 018000005017
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0413-2025·2025-08-13

    Silk vanilla almondmilk recalled after a shipping trailer temperature excursion

    Silk Vanilla AlmondMilk, 64 fl oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Silk Vanilla AlmondMilk, 64 FL OZ (2 QT) 1.89 L, packaged in a paper carton, UPC: 025293000995
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0388-2025·2025-08-13

    Boar's Head chevre goat cheese packages carry an incorrect use by date

    Boar's Head Chevre Goat Cheese Cranberry Cinnamon, 4 oz, is being recalled because the package has an incorrect use by date. 372 cases are affected.

    Product
    Boar's Head Chevre Goat Cheese Cranberry Cinnamon, Net Wt 4 oz (113g). UPC 0 42421-15231 9. Keep Refrigerated. Distributed By: Brunckhorst Co., NY, NY 11206-3886.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0417-2025·2025-08-13

    Yoplait Harvest Peach yogurt recalled after a shipping trailer temperature excursion

    Yoplait Original Harvest Peach Yogurt, 6 oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Yoplait Original Harvest Peach Yogurt, 6 OZ (170g), packaged in a plastic cup, UPC: 170470003075
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2256-2025·2025-08-13

    Laparoscopy packs contain an inadvertently resterilized visualization system

    Laparoscopy Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 452 units are affected.

    Product
    LAPAROSCOPY PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • SevereNHTSA·25V525000·2025-08-12

    Heil Recalls 2018-2020 Front End Loader Garbage Trucks Due to Fire Risk

    The Heil Co. is recalling 2018-2020 front end loader garbage trucks because excessive vibrations may cause hydraulic tubes to leak, increasing the risk of fire.

    Product
    HEIL — HEIL FRONT END LOADER GARBAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V522000·2025-08-12

    IC Bus school bus parking brake springs may corrode and break

    International is recalling certain 2024-2026 IC Bus CESB and 2025 EVSB school buses because the parking brake tension spring may corrode and break, disengaging the parking brake. 3,230 buses affected.

    Product
    IC BUS — IC BUS CESB, EVSB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V524000·2025-08-12

    Heil Recalls 2021-2022 Front End Loader Garbage Trucks Due to Weld Defect

    The Heil Co. is recalling 2021-2022 front end loader garbage trucks because missing vertical welds on the automatic front loader arm may cause it to crack and fall, increasing injury risk.

    Product
    HEIL — HEIL FRONT END LOADER GARBAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V523000·2025-08-12

    Heil Recalls 2024 Front End Loader Garbage Trucks for Fuel Solenoid Defect

    The Heil Co. is recalling 2024 front end loader garbage trucks because a fuel shutoff solenoid may fail, causing the engine to stall while driving and increasing crash risk.

    Product
    HEIL — HEIL FRONT END LOADER GARBAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V520000·2025-08-11

    Volvo New VN Trucks Recalled Due to Potential Loss of Steering Control

    Volvo Trucks North America is recalling certain 2025-2026 Volvo New VN trucks because the dynamic steering and oversteer guidance feature may malfunction, increasing the risk of a crash.

    Product
    VOLVO — VOLVO VNL (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V513000·2025-08-08

    Ford Recalls 2021 Mustang Mach-E for Brake Software Update

    Ford is recalling 2021 Mustang Mach-E vehicles to update ABS software that may disable power brake assist and stability controls, increasing crash risk.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V514000·2025-08-08

    Land Rover Recalls 2014-2017 Range Rovers for Suspension Defect

    Jaguar Land Rover is recalling 2014-2017 Range Rover and Range Rover Sport vehicles because a front suspension part may crack, risking loss of control.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V512000·2025-08-08

    Ford Recalls 2023-2025 F-150 Trucks for Rear Axle Hub Bolt Defect

    Ford is recalling 2023-2025 F-150 trucks with specific towing packages because a rear axle hub bolt may break, potentially causing loss of drive power or vehicle rollaway.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V518000·2025-08-08

    Lincoln Nautilus power windows may not reverse correctly after obstruction

    Ford is recalling certain 2024-2025 Lincoln Nautilus vehicles repaired incorrectly under a previous recall because the window automatic reversal system may not react correctly to an obstruction. 482 vehicles affected.

    Product
    LINCOLN — LINCOLN NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V517000·2025-08-08

    Ford Recalls 2022 F-150s for Flickering Parking Lights

    Ford is recalling 2022 F-150 vehicles previously repaired under recall 22V686 because the parking lights may flicker when headlights are activated.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V511000·2025-08-08

    Mercedes-Benz Recalls 2024 GLA Models for Headlight Aim Markings

    Mercedes-Benz is recalling 2024 GLA 250 and AMG GLA 35 4MATIC vehicles because missing headlight aim markings may cause improper aiming, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLA 35 4MATIC, GLA 250 4MATIC, GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V515000·2025-08-08

    Ford Recalls 2022 F-150s for Flickering Parking Lights

    Ford is recalling 2,361 2022 F-150 vehicles because incorrectly repaired parking lights may flicker, reducing visibility and increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V510000·2025-08-08

    Lincoln Corsair rearview cameras can take in water at the connectors

    Ford is recalling certain 2020-2022 Lincoln Corsair vehicles because water may enter the rearview camera connectors, causing the image not to appear or to display distorted. 41,875 vehicles affected.

    Product
    LINCOLN — LINCOLN CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V509000·2025-08-08

    Altec Recalls 2025 AP Series Vehicles Due to Brake Line Defect

    Altec is recalling 2025 AP Series vehicles because brake air line fittings may not be tightened correctly, potentially causing the emergency brakes to engage unexpectedly.

    Product
    ALTEC — ALTEC AP SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V516000·2025-08-08

    One Ford Mustang instrument cluster may fail to illuminate at startup

    Ford is recalling one 2024 Mustang that was repaired incorrectly under a previous recall because the Instrument Panel Cluster may not illuminate at startup or while driving.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V519000·2025-08-08

    Ford and Lincoln LED driver modules may contain a burnt diode

    Ford is recalling certain 2025 Lincoln Nautilus, Mustang Mach E and Mustang vehicles because LED Driver Modules may contain a burnt diode, causing headlights and other exterior lights to fail. 3,270 vehicles affected.

    Product
    FORD — FORD, LINCOLN MUSTANG, MUSTANG MACH E, NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25428·2025-08-07

    Altafit af28 smartwatch charging pads can overheat and catch fire

    Altafit af28 smartwatches are being recalled because the wireless charging pad can overheat and ignite. Thirty-nine reports include six burns to hands and property damage. About 2,900 units affected.

    Product
    Altafit af28 Smartwatches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25425·2025-08-07

    LeymanKids children's pajama sets fail the sleepwear flammability standard

    LeymanKids children's two-piece pajama sets are being recalled because they violate the mandatory flammability standards for children's sleepwear. About 600 units are affected.

    Product
    LeymanKids Children's Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25426·2025-08-07

    Séfralls minoxidil hair serum lacks the required child-resistant packaging

    Séfralls Hair Generation Serum is being recalled because it contains minoxidil, which must be in child-resistant packaging under the Poison Prevention Packaging Act. About 21,300 units affected.

    Product
    Séfralls Minoxidil Hair Generation Serum
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25427·2025-08-07

    La Ligne Enfant children's pajamas fail the sleepwear flammability standard

    La Ligne Enfant Bonne Nuit children's cotton pajama sets are being recalled because they violate mandatory standards for children's sleepwear flammability. About 1,185 units are affected.

    Product
    La Ligne Enfant Bonne Nuit Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25424·2025-08-07

    Monica Vinader gold mini heart jewelry can contain excess cadmium

    Monica Vinader 14k Yellow Gold Mini Heart bracelets, necklaces and stud earrings are being recalled because the jewelry can contain excess levels of cadmium. About 300 units are affected.

    Product
    Monica Vinader 14k Yellow Gold Mini Heart Jewelry
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V507000·2025-08-07

    Mitsubishi Outlander PHEV liftgate gas spring cylinders corrode unexpectedly

    Mitsubishi is recalling certain 2018–2022 Outlander PHEV and 2014–2020 Outlander vehicles because liftgate gas spring cylinders may corrode, lose pressure, rupture, or cause the liftgate to fall unexpectedly, creating injury risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V505000·2025-08-07

    Suzuki Recalls Motorcycles for Excessively Bright Headlights

    Suzuki is recalling 2020-2025 DL1050 and 2020/2024 GSX-S1000S motorcycles because the upper headlight beam may be too bright, potentially blinding oncoming drivers.

    Product
    SUZUKI — SUZUKI GSX-S1000S, DL1050
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25422·2025-08-07

    TEMI Go Basketball toys contain small balls banned for young children

    TEMI Toys Go Basketball children's toys are being recalled because the toy contains small balls and is intended for children under three, violating the small ball ban. About 660 units affected.

    Product
    TEMI Go Basketball Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25421·2025-08-07

    Pet Zone laser pointer toys expose button cell batteries when broken

    Pet Zone Laser Pointer & LED Ball pet toys are being recalled because the LED sphere can break on impact, making the button cell batteries easily accessible to children. About 15,400 units affected.

    Product
    Pet Zone Laser Pointer & LED Ball Pet Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V508000·2025-08-07

    2025 Nissan Frontier Daytime Running Lights Software Error

    Nissan is recalling certain 2025 Nissan Frontier vehicles due to a software logic error that may cause daytime running lights to dim unexpectedly when the idle start-stop feature cycles the engine, posing a crash risk.

    Product
    NISSAN — NISSAN FRONTIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0332-2025·2025-08-06

    Sheehan Brothers spicy chicken sandwiches recalled over undeclared sesame

    Sheehan Brothers Vending Spicy Chicken Sandwiches, 6.5 oz, are being recalled because of undeclared sesame. 600 individual units are affected.

    Product
    Sheehan Brothers Vending Spicy Chicken Sandwich, 6.5 oz (184g), individually wrapped in plastic, UPC: 100000222539
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·H-0335-2025·2025-08-06

    Sheehan Brothers chili cheese coneys recalled over undeclared sesame

    Sheehan Brothers Vending Chili Cheese Coneys, 4.3 oz, are being recalled because of undeclared sesame. 377 individual units are affected.

    Product
    Sheehan Brothers Vending Chili Cheese Coney, 4.3 oz (120g), in a red and white paper boat and individually wrapped in plastic, UPC: 100000222027
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2158-2025·2025-08-06

    SafeStar 90 Plus breathing filters show a slow rising CO2 curve

    SafeStar 90 Plus bidirectional breathing system filters are being recalled following reports of a slow increase of the CO2 curve when the gas sample is taken from the filter's gas sampling port. 669,838 units affected.

    Product
    SafeStar 90 Plus Filter. Bidirectionally breathing system filter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0348-2025·2025-08-06

    Lespoir cookies recalled over undeclared milk on the label

    Lespoir cookies, net weight 1.41 oz, are being recalled because of undeclared milk. 32 units are affected.

    Product
    Lespoir cookie, net weight: 1.41 oz. UPC# 4 942737 200147
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·H-0426-2025·2025-08-06

    Newly Weds panko bread crumbs recalled over potential Listeria contamination

    Newly Weds Panko Japanese Style Untoasted Bread Crumbs in 25 lb units are being recalled because of potential Listeria monocytogenes contamination. 73,750 lbs are affected.

    Product
    Newly Weds A60447-PANKO JAPANESE STYLE UNTOASTED BREAD CRUMBS-NET WT 25 LBS.
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-2164-2025·2025-08-06

    Automated Impella Controllers may not detect a connected Impella pump

    The Automated Impella Controller, used with left heart support blood pumps, is being recalled because of a potential issue with the controller not detecting an Impella pump when it is connected. 11,031 units affected.

    Product
    Automated Impella Controller (AIC), used in left heart support blood pump, including the following: 1. Impella Controller, Packaged, AU; Product Code: 0042-0000-AU. 2. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 3. Impella Controller, Packaged, EU; Pr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V503000·2025-08-06

    IC Bus CESB School Buses Brake Pressure Switch Fire Risk Recall

    International Motors is recalling certain 2016–2024 IC Bus CESB school buses because the brake pressure switch assembly may leak brake fluid into electrical components, causing a short circuit and fire risk while driving or parked.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide

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