The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

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All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

7401–7425 of 89525

  • HighFDA (Devices)·Z-1592-2025·2025-04-23

    Medline Sterile Convenience Kits Recalled for Potential Weak Seals

    Medline Industries is recalling multiple sterile surgical convenience kits because purchased breather pouches used in packaging may have open or weak seals, which could compromise sterility.

    Product
    Medline Convenience kits used for various procedures: 1) DR. KHAN CABG ADDS PACK, Model Number: DYNJ59310D; 2) CARDIAC STERNAL PACK, Model Number: DYNJ32436A; 3) VEIN CLOSURE PACK, Model Number: DYNJ35586G; 4) ABLATION PACK-LF, Model Number: DYNJ55343B; 5) ABLATION PACK-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1552-2025·2025-04-23

    BD Pyxis MedBank Receiving Cabinet Software Medication Dispensing Safety Issue

    CareFusion 303 is recalling certain BD Pyxis MedBank Receiving Cabinet Software versions because a "Clear All" function may bypass pharmacist validation, potentially allowing incorrect medication dispensing without authorization.

    Product
    MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLEX 2.0, REF: 1139-00; MEDBANK TOWER MAIN, REF: 1145-00; MEDBANK MINI MAIN, REF: 1147-00 BD PYXIS MEDBANK Facility Software, REF: 139090-01; BD PYXS MEDBNK TWR MN 2HH1FH2HM2FM2FG1FF, REF: 169-100; BD PYXIS MEDBANK MINI 1HH-1F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0713-2025·2025-04-23

    Tony's Chocolonely Everything Bar recalled for foreign objects

    Tony's Chocolonely Inc is recalling Tony's Chocolonely Everything Bar products nationwide due to the presence of stones in the chocolate bars.

    Product
    Tony's Chocolonely Everything Bar
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1614-2025·2025-04-23

    Medline Sterile Procedure Kits recalled for potential seal issues

    Medline Industries is recalling multiple sterile procedure kits due to potential open or weak seals on breather pouches used for packaging. The affected kits were distributed worldwide including the US and several other countries.

    Product
    Medline Convenience kits used for various procedures: 1) ED CRASH C-SECTION TRAY, Model Number: MNS13635A; 2) C-SECTION PCH-LF, Model Number: DYNJ81281; 3) C-SECTION PACK-LF, Model Number: OBK387M; 4) C-SECTION PCH-LF, Model Number: DYNJ81281; 5) NHS - C-SECTION SCG, Mod
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1555-2025·2025-04-23

    GE Venue Go Ultrasound Systems Battery Risk Recall

    GE Medical Systems is recalling certain Venue Go ultrasound system models worldwide due to potential battery internal failure that could result in smoke or fire.

    Product
    Venue Go Models: R2 (Model Number H45181VG), R3 (Model Number H45193VG), R4 (Model Number H45114VG), R5 (Model Numbers H45135VG, H45135VGW), R3 Surgery for China (Model Number H45113VGSU), R3 PeriOP for China (Model Number H45113VGPO), R3 Expert for China (Model Number H45113VGEX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0710-2025·2025-04-23

    Salvadorena Quesadilla de Queso Recalled for Undeclared Milk

    Panaderia Salvadorena Ii is recalling Quesadilla de Queso products that contain undeclared milk, a common allergen that poses a risk to consumers with milk allergies.

    Product
    PANADERIA/BAKERY Salvadorena; Quesadilla de Queso; Ingredients: Rice, Wheat Flour, soy, eggs, sugar, butter, baking powder, salt, water, sour cream, sesame seeds; UPC 0 21651 16499 6; NET WEIGHT APPROX 14 OZ
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1611-2025·2025-04-23

    Medline Convenience Kits for Obstetrical Procedures Recalled for Weak Seals

    Medline Industries is recalling 21,935 units of sterile convenience kits used for labor, delivery, and vaginal delivery procedures due to potential open or weak seals on breather pouches. The defective packaging could compromise product sterility.

    Product
    Medline Convenience kits used for various procedures: 1) LABOR AND DELIVERY PACK-LF, Model Number: DYNJ26971L; 2) VAGINAL DELIVERY PACK-LF, Model Number: DYNJ0378319P; 3) VUWC OB PACK, Model Number: DYNJ64017B; 4) OB PROTECTION PACK NO GAUZE, Model Number: DYNJHTLD04A; 5
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1612-2025·2025-04-23

    Medline Convenience Kits Recalled for Potential Open Breather Pouch Seals

    Medline Industries is recalling select sterile convenience kits (Model DYNJ80807B, Lot 24IBH993) due to potential open or weak seals on breather pouches used for packaging. Compromised seals may affect product sterility.

    Product
    Medline Convenience kits used for various procedures: 1) CW PERI GYN, Model Number: DYNJ80807B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0704-2025·2025-04-23

    Trader Joe's Hot Honey Mustard Dressing Recalled for Undeclared Allergens

    Trader Joe's Hot Honey Mustard Dressing (12 fl. oz., Use By Date 5/27/25) is being recalled because bottles labeled as Hot Honey Mustard actually contain Thai Style Peanut Dressing with undeclared peanuts, soy, sesame, and wheat.

    Product
    Trader Joe's Hot Honey Mustard Dressing (SKU #80152), packaged in glass bottle with tamper overwrap on plastic cap, net wt. 12 fl. oz. UPC 0080 1522. DIST. & SOLD Exclusively by: Trader Joe's Monrovia, CA. These 12oz. bottles were sold directly to consumers. The master cases we
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-1562-2025·2025-04-23

    Welch Allyn Connex Wall System blood pressure cuffs recalled for undeclared rubber

    Baxter Healthcare is recalling certain Welch Allyn Connex Integrated Wall System blood pressure cuff configurations due to an undeclared natural rubber band in the packaging that may cause allergic reactions in individuals with latex sensitivity.

    Product
    Welch Allyn Connex Integrated Wall System, Product Code/Part Numbers: 1) 84MTVE2-4; 2) 84MTVE2-6; 3) 84MTVE2-B; 4) 84MTVE2-US; 5) 84MTVEC-6; 6) 84MTVEC-B; 7) 84MTVEP-B; 8) 84MTVEX-4; 9) 84MTVX2-4; 10) 84MTVX2-6; 11) 84MTVX2-B; 12) 84MTVX2-US; 13) 84MTVX
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1621-2025·2025-04-23

    Guide Wire with Ruler Tube metal ring detachment recall

    Stryker GmbH is recalling Guide Wire with Ruler Tube 3x1000 mm DIA devices because the metal ring at the end may detach during surgery.

    Product
    Guide Wire with Ruler Tube 3x1000 mm DIA; Catalog number/REF: 2351-3100S;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V270000·2025-04-23

    Ford Recalls 2015 Models for Rearview Camera Defect

    Ford is recalling 2015 F-Series, Expedition, Navigator, and MKC vehicles because a loose rearview camera connector may cause a blank or distorted image, increasing crash risk.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR, MKC, redundant F-250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V268000·2025-04-22

    Utilimaster Aeromaster Recall for Improperly Tightened Seat Fasteners

    Shyft Group is recalling 2022-2025 Utilimaster Aeromaster vehicles because suspension seat mounting fasteners may be improperly tightened, increasing injury risk in a crash.

    Product
    UTILIMASTER — UTILIMASTER AEROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V266000·2025-04-22

    IC school bus driver seat belt anchor bolts may come loose

    International is recalling certain 2025-2026 IC CESB and 2025 EVSB school buses because the driver's seat belt anchor bolt may come loose, so the belt may not restrain the driver in a crash.

    Product
    IC BUS — IC BUS CESB, EVSB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25C006000·2025-04-22

    Dorel Safety 1st Child Seat Recall for Loose Headrest Foam

    Dorel Juvenile Group is recalling Safety 1st Grow & Go Sprint child seats because the headrest foam pad is not adequately secured, posing a choking hazard.

    Product
    CHILD SEAT:MATERIAL/PADDING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V262000·2025-04-21

    Motiv Recalls 2020 F-59 School Buses Due to Power Bracket Defect

    Motiv Power Systems is recalling 2020 F-59 BEV chassis school buses because a support bracket may break, causing an electrical short and loss of drive power.

    Product
    MOTIV — MOTIV F-59 BEV CHASSIS SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V265000·2025-04-21

    Highland Ridge Recalls 2025 GO Play Travel Trailers for Label Errors

    Highland Ridge RV is recalling 2025 GO Play travel trailers because incorrect weight and tire labels may lead to overloading and crashes.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT GO PLAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-04192025-01·2025-04-19

    Cargill Pork Carnitas Recalled for Possible Metal Contamination

    USDA FSIS issued a public health alert for Cargill pork carnitas potentially contaminated with metal pieces. No injuries have been reported.

    Product
    Cargill Meat Solutions — FSIS Issues Public Health Alert for Pork Carnitas Products Due to Possible Extraneous Material Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V263000·2025-04-18

    Motorhome slide-room floor may not retain seat belts in a crash

    Forest River is recalling certain 2025 East to West Bravado BRC33DSF motorhomes because the slide-room floor may detach in the open position and may not properly retain the seat belts during a crash.

    Product
    EAST TO WEST — EAST TO WEST BRAVADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V261000·2025-04-18

    Motiv Recalls F-53 and F-59 Chassis Due to Bracket Failure Risk

    Motiv Power Systems is recalling 2019-2022 F-53 and F-59 chassis vehicles because a support bracket may break, causing an electrical short and loss of drive power.

    Product
    MOTIV — MOTIV F-53 BEV CHASSIS, F-59 BEV CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V264000·2025-04-18

    Forest River trailer accent lights and awning wiring lack circuit protection

    Forest River is recalling certain 2024-2025 Aurora and Coachmen Catalina travel trailers because the front accent lights, awning and auto-levelling system may be incorrectly wired without overcurrent protection.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN AURORA, CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V256000·2025-04-17

    Mack Recalls 2025 Anthem Trucks Due to Engine Gear Bracket Defect

    Mack Trucks is recalling 2025 Anthem vehicles because improperly tightened idler gear bracket fasteners may allow the gear to detach, potentially causing an engine stall and increasing crash risk.

    Product
    MACK — MACK ANTHEM (AN)
    Category
    Vehicle
    Distribution
    Distributed nationwide