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 the agency’s own highest classification or reported deaths or serious injuries, 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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3651–3675 of 39747

  • CriticalFDA (Food)·F-0217-2025·2024-11-27

    Frozen U-BAKE Apple Pie recalled for undeclared egg allergen

    Grand Central Bakery FRE Co Inc is recalling 150 packages of U-BAKE Apple Pie due to undeclared egg. The product label declares wheat and milk but not egg, posing a serious risk to consumers with egg allergies.

    Product
    U-BAKE Apple Pie, frozen product and packaged in LDPE bag, net wt. 2lbs. 9oz. Made by Grand Central Baking Company. Label declares Wheat and Milk.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0143-2025·2024-11-27

    Chicken Alfredo Kit Recalled Due to Listeria Contamination

    Joseph Seviroli, LLC is recalling Chicken Alfredo Kit due to potential Listeria monocytogenes contamination in the chicken. The product was distributed across multiple states.

    Product
    Chicken Alfredo Kit
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Devices)·Z-0373-2025·2024-11-27

    Peritoneal Dialysis Transfer Set Recalled for PCB Contamination Risk

    Baxter Healthcare recalls peritoneal dialysis transfer sets (Part Number 5C4482) due to potential contamination with polychlorinated biphenyls (PCBs). The recall affects 2.7 million units distributed worldwide.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V896000·2024-11-27

    Chrysler Recalls 2017-2018 Ram Trucks Due to Brake Control Unit Failure

    Chrysler is recalling 2017-2018 Ram 2500, 3500, 4500, and 5500 trucks because the hydraulic control unit may fail, disabling anti-lock brakes and stability controls.

    Product
    RAM — RAM 5500, 2500, 4500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0381-2025·2024-11-27

    Baxter MiniCap PD Transfer Set Recalled for Potential Chemical Exposure Risk

    Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to polychlorinated biphenyls.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0218-2025·2024-11-27

    Frozen Pie Crust and Bulk Dough Recalled for Undeclared Egg

    Grand Central Bakery is recalling U-BAKE frozen pie crust and bulk pie dough because they contain undeclared egg. The recall affects products distributed in Oregon and Washington.

    Product
    U-BAKE Pie Crust (Pastry Round), frozen product and packaged in LDPE bag, 2-10.5 inch pie crust per package, net wt. 20oz. Made by Grand Central Baking Company. Label declares Wheat and Milk. Bulk pie dough rolls, packaged in plastic wrap and parchment paper, net wt. 10lbs.…
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0379-2025·2024-11-27

    Baxter MiniCap Dialysis Transfer Sets Recalled for PCB Exposure Risk

    Baxter is recalling MiniCap Extended Life PD Transfer Sets used in peritoneal dialysis due to potential exposure to polychlorinated biphenyls (PCBs). About 62,394 units distributed worldwide may be affected.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4483; use in Peritoneal Dialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0375-2025·2024-11-27

    Baxter peritoneal dialysis transfer set recalled for PCB exposure risk

    Baxter MiniCap Extended Life PD Transfer Sets (Part 5C4482S) are being recalled due to potential exposure to polychlorinated biphenyls (PCBs). The FDA Class I recall affects 151,020 units distributed worldwide.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0380-2025·2024-11-27

    Baxter MiniCap Peritoneal Dialysis Transfer Set Recalled for Chemical Exposure Risk

    Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to non-dioxin-like polychlorinated biphenyls.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4484; use in Peritoneal Dialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0219-2025·2024-11-27

    FDA Recalls U-BAKE Frozen Marionberry Pie for Undeclared Egg

    Grand Central Bakery is recalling U-BAKE Marionberry Pie due to undeclared egg, a major allergen not listed on the label. The recall affects 336 packages distributed in Oregon and Washington with expiration dates from February 1 to April 17, 2025.

    Product
    U-BAKE Marionberry Pie, frozen product and packaged in LDPE bag, net wt. 2lbs. 4oz. Made by Grand Central Baking Company. Label declares Wheat and Milk.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0220-2025·2024-11-27

    Frozen Chicken Pot Pie Recalled for Undeclared Egg Allergen

    U-BAKE Chicken Pot Pie frozen packages are being recalled because they contain undeclared egg, a common allergen. Consumers with egg allergies should not consume this product.

    Product
    U-BAKE Chicken Pot Pie, frozen product and packaged in heat-sealable polypropylene film. Net wt. 11.5oz. Made by Grand Central Baking Company. Label declares Wheat and Milk.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0482-2025·2024-11-27

    Medical Device Recall: Counterfeit Batteries in Plum Infusion Systems

    Counterfeit CSB batteries are being used in Plum Infusion Systems. These unauthorized batteries fail to hold their charge and have not been tested for use with the pumps.

    Product
    Allegedly counterfeit batteries manufactured by CSB batteries being used with Plum Infusion Systems: Plum 360" Infusion System, Pump List Number 30010; Plum A+ & Plum A+3" Infusion Systems, Pump List Numbers: 11005, 11971, 12391, 12618, 20678, 20679, 20792, 60529, 12348, 1197
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V897000·2024-11-27

    Jeep Grand Cherokee side airbags may not deploy in a crash

    Chrysler is recalling certain 2022-2024 Grand Cherokee and 2021-2024 Grand Cherokee L vehicles because an improperly secured connector may prevent the front seat side airbags deploying. All units have been remedied.

    Product
    JEEP — JEEP GRAND CHEROKEE L, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0374-2025·2024-11-27

    Baxter MiniCap Peritoneal Dialysis Transfer Set Recalled for Chemical Exposure Risk

    Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to polychlorinated biphenyls found in similar devices.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V900000·2024-11-27

    Honda Passport and Pilot fuel filler pipes can separate and leak

    Honda is recalling certain 2023-2024 Passport and 2023-2025 Pilot vehicles because the fuel filler neck tube and fuel filler pipe may separate, allowing fuel to leak.

    Product
    HONDA — HONDA PASSPORT, PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0376-2025·2024-11-27

    Baxter MiniCap PD Transfer Set Recalled for Potential PCB Exposure

    Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to non-dioxin-like polychlorinated biphenyls.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4483; use in Peritoneal Dialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V899000·2024-11-27

    Keystone Recalls 2025 Arcadia and Cougar Trailers for Hitch Fastener Issue

    Keystone is recalling 2025 Arcadia and Cougar trailers because improperly tightened pin box fasteners may loosen, allowing the trailer to detach and increasing crash risk.

    Product
    KEYSTONE — KEYSTONE COUGAR, ARCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0378-2025·2024-11-27

    Baxter MiniCap Peritoneal Dialysis Transfer Set recalled for potential PCB exposure

    Baxter Healthcare is recalling 58,680 units of its MiniCap Extended Life PD Transfer Set due to potential exposure to polychlorinated biphenyls (PCBs). Users should stop using affected units and consult their healthcare provider.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482E; use in Peritoneal Dialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0377-2025·2024-11-27

    Baxter Peritoneal Dialysis Transfer Set Recalled for PCB Contamination Risk

    Baxter Healthcare is recalling the MiniCap Extended Life PD Transfer Set due to potential exposure to polychlorinated biphenyls (PCBs). Approximately 410,862 units are affected.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V890000·2024-11-25

    Winnebago Ekko motorhomes may be missing spare tire wheel bolts

    Winnebago is recalling certain 2024-2025 Ekko motorhomes because the wheel bolts for the spare tire may be missing. 632 units are affected.

    Product
    WINNEBAGO — WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V884000·2024-11-22

    Forest River Recalls 2024-2025 Viking and Clipper Travel Trailers

    Forest River is recalling 2024-2025 Viking and Clipper travel trailers because a fresh water tank support bracket may break, increasing crash risk.

    Product
    VIKING TRAVEL TRAILERS — VIKING TRAVEL TRAILERS, FOREST RIVER VIKING, CLIPPER CAMPING TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V885000·2024-11-22

    Brinkley Model Z fifth wheel pin box fasteners may be undertightened

    Brinkley RV is recalling certain 2024-2025 Model Z fifth wheel trailers with Curt Helux pin boxes because the pin box fasteners may have been improperly tightened.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25052·2024-11-21

    Segway Ninebot P100 KickScooters Recalled for Broken Front Fork and Fall Hazards

    Segway is recalling about 1,400 Ninebot P100 KickScooters because the front fork can break, causing falls and injuries. The company has received 31 reports of fork breakage, including 6 reports of injuries such as fractures, cuts, scrapes, bruises, and shoulder pain.

    Product
    Segway Ninebot P100 KickScooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide