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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2451–2475 of 39704

  • SevereFDA (Food)·H-0316-2025·2025-07-23

    Peeters Mushroom Farm cremini sliced mushrooms recalled over potential Listeria contamination

    Peeters Mushroom Farm Cremini Sliced Mushrooms in 8 oz packages are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 25 cases are affected.

    Product
    Peeters Mushroom Farm Cremini Sliced mushrooms 227g (8 oz.) UPC 0 68414 96960 3, flat black plastic package, BEST BEFORE 25JL04 stamped on side, 12 packages per case
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·H-0262-2025·2025-07-23

    Shredded red cabbage recalled over potential Listeria monocytogenes contamination

    Shredded red cabbage packed in polybags and cardboard cases is being recalled because it has the potential to be contaminated with Listeria monocytogenes. One 14 lb case is affected.

    Product
    Red cabbage, shredded packed in polybag and cardboard case. 14 lbs per case.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0263-2025·2025-07-23

    Diced red onions recalled over potential Listeria monocytogenes contamination

    Diced red onions packed in polybags and cardboard cases are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 8 cases are affected.

    Product
    FG20001 Onion, Red Diced packaged in poly bag and cardboard case. 18 lbs per case
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0283-2025·2025-07-23

    Kilwin's family assortments recalled over undeclared pecans in the product

    Kilwin's Family Assortment in 9 oz, 14 oz, 28 oz and 42 oz sizes is being recalled because of undeclared pecans. 130 lbs in total are affected.

    Product
    Kilwin's Family Assortment 9oz UPC 0 004564 3 Kilwin's Family Assortment 14oz UPC 0 004565 0 Kilwin's Family Assortment 28oz UPC 0 004566 7 Kilwin's Family Assortment 42oz UPC 0 004567 4
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Food)·H-0282-2025·2025-07-23

    Kilwin's truffle assortments recalled over undeclared pecans in the product

    Kilwin's Truffle Assortments in 9.5 oz, 8 oz and 4.75 oz sizes are being recalled because of undeclared pecans. 130 lbs in total are affected.

    Product
    Kilwin's Truffle Assortment 9.5oz UPC 0 004574 0 Kilwin's Truffle Assortment 8oz UPC 0 043109 5 Kilwin's Truffle Assortment 4.75oz UPC 0 044121 8
    Category
    Food
    Distribution
    14 states
  • SevereNHTSA·25V479000·2025-07-23

    Ferrari Purosangue fuse box contact can decrease braking ability

    Ferrari is recalling certain 2023-2025 Purosangue vehicles because the fuse box power supply and passenger-side footrest may contact each other, causing a short circuit that decreases braking ability.

    Product
    FERRARI — FERRARI PUROSANGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V478000·2025-07-22

    Winnebago airbag wiring can be caught in the seat mechanism

    Winnebago is recalling certain 2024-2026 motorhomes because Supplemental Restraint System wires can be caught in the seat mechanism when the front seats are adjusted, damaging them.

    Product
    WINNEBAGO — WINNEBAGO VIEW, REVEL, EKKO, NAVION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V476000·2025-07-22

    Nova Bus steering can turn without driver input from missing valve

    Nova Bus is recalling certain 2020-2023 LFS transit buses because the electric power steering system may be missing a check valve, allowing hydraulic pressure to turn the steering wheel on its own.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·25393·2025-07-21

    Above-ground pools recalled after nine children drowned using strap footholds

    Above-ground pools 48 inches and taller with compression straps over the vertical support legs are being recalled because the strap can create a foothold. CPSC believes nine children have drowned.

    Product
    48-inch and taller above-ground pools with compression straps running on the outside and over the vertical support legs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25390·2025-07-17

    iStore magnetic wireless power banks can overheat and ignite while charging

    iStore Magnetic Wireless Power Banks, model IST-09991/W05, are being recalled because the lithium-ion battery can overheat and ignite while charging. Three incidents and about $15,000 in property damage reported.

    Product
    iStore Magnetic Wireless Power Banks (IST-09991/W05 model only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25391·2025-07-17

    VIVI e-bike lithium-ion batteries can overheat, posing fire and burn hazards

    36-volt lithium-ion batteries supplied with certain VIVI e-bikes are being recalled because they can overheat. Fourteen overheating incidents including three fires have been reported. About 24,000 units affected.

    Product
    36-volt lithium-ion batteries used with VIVI E-bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·026-2025·2025-07-17

    Kayem Foods Recalls Chicken Sausage Due to Plastic Contamination

    Kayem Foods is recalling ready-to-eat chicken sausage products nationwide due to possible contamination with pieces of plastic.

    Product
    Kayem Foods Inc. — Kayem Foods Inc. Recalls Ready-To-Eat Chicken Sausage Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V473000·2025-07-17

    Grand Design trailer entrance door latch mechanism may fail

    Grand Design is recalling certain 2025-2026 Lineage trailers with Lippert Modularia entrance doors because the door latch mechanism may fail, potentially trapping occupants in an emergency.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25389·2025-07-17

    CasaClean handheld steamers can leak steam or spew hot boiling water

    CasaClean Handheld Steamers, model DF-958, are being recalled because they can leak steam or spew hot boiling water. Thirteen consumers have received burns. About 23,000 units are affected.

    Product
    CasaClean Handheld Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25387·2025-07-17

    Traveller aluminum loading ramps can bend or break under rated loads

    Traveller aluminum loading ramps are being recalled because they cannot withstand the weight specified on the ramps and can bend or break in use. Two injuries have been reported. About 18,000 units affected.

    Product
    Traveller Aluminum Loading Ramps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2031-2025·2025-07-16

    Hillrom Q-Link 13 patient lift components may falsely latch and detach

    The Hillrom Q-Link 13 component used with mobile patient lifts is being recalled because it may allow false latching of the quick-release hook. 9,899 units are affected.

    Product
    Hillrom Q-Link 13 component, Product Code 3156509, used with the following Mobile Patient Lifts: 1) Uno 102 EE Mobile lift - Product Code 2010004; 2) Viking L Mobile lift - Product Code 2040044; 3) Viking XL Mobile lift - Product Code 2040043; 4) Viking M Mobile lift…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·H-0221-2025·2025-07-16

    Whole organic celery seed recalled over potential Salmonella contamination

    Whole Organic Celery Seed is being recalled because of potential contamination with Salmonella. 439 bags totalling 24,694 lbs are affected.

    Product
    Celery Seed Whole Organic, labeled, "CELERY SEED WHL OG; Net Wt: 56.25 Lbs"
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2081-2025·2025-07-16

    Optisite OPTI18 arterial cannulas may have wire protruding from the body

    Edwards Optisite OPTI18 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 13,240 units affected.

    Product
    Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI18 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2032-2025·2025-07-16

    Hillrom LikoScale patient lift components may falsely latch and detach

    Hillrom LikoScale components used with patient lift adapter kits are being recalled because the Q-link 13 may allow false latching of the quick-release hook. 9,839 units are affected.

    Product
    Hillrom LikoScale component, Product Code 3156232, used with the following adapter kits for patient lifts: 1) LikoScale 200 Accessory - Product Code 3156225; 2) LikoScale 350 Accessory - Product Code 3156228; 3) LikoScale 400 Accessory - Product Code 3156226.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·H-0215-2025·2025-07-16

    Weaver bulk semi-sweet chocolate nonpareils recalled over undeclared milk allergen

    Weaver Chocolates Nonpareil Semi-Sweet Chocolate in 25 lb bulk cases is being recalled because of an undeclared milk allergen. 849 cases are affected.

    Product
    Weaver Chocolates, 47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds) - 25 lbs. Bulk Cases
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Devices)·Z-2084-2025·2025-07-16

    FEM-FLEX II FEMII018A cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII018A, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 13,240 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2085-2025·2025-07-16

    FEM-FLEX II FEMII018AS cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII018AS, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 558 units affected.

    Product
    Brand Name: FEM-FLEXII Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018AS Software Version: N/A Product Description: The Edwards FEMFLEXII Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2080-2025·2025-07-16

    Optisite OPTI16 arterial cannulas may have wire protruding from the body

    Edwards Optisite OPTI16 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 27,022 units affected.

    Product
    Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI16 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2083-2025·2025-07-16

    FEM-FLEX II femoral arterial cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 847 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016AS Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.…
    Category
    Medical Device
    Distribution
    Distributed nationwide