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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2076–2100 of 89459

  • SevereNHTSA·26V276000·2026-04-30

    Grand Design Lineage solar panels may detach from the roof

    Grand Design is recalling certain 2025-2026 Lineage recreational vehicles because the adhesive securing the roof solar panels may fail, allowing a panel to detach into the roadway.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V275000·2026-04-30

    Nova Bus LFS transit buses may lose drive power from data overload

    Nova Bus is recalling certain 2022-2023 LFS transit buses because a telemetry control unit may cause a data overload, shutting down the unit and causing a loss of drive power.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26453·2026-04-30

    Acer folding electric scooter front tube can fold down unexpectedly

    Acer AES015 folding electric scooters are recalled because a loose screw can cause the front tube to fold down unexpectedly, posing a fall hazard. About 510 US units are affected.

    Product
    Acer AES015 Two-Wheeled Folding Electric Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26450·2026-04-30

    Residential elevator StrikeLock devices may let the cab move with doors open

    StrikeLock hoistway door locking devices for residential elevators are recalled because they can allow the elevator cab to move with a landing door open, posing a fall hazard.

    Product
    Residential Elevators StrikeLock Hoistway Door Locking Device
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26454·2026-04-30

    Qumeney bicycle light sets let children access button cell batteries

    Qumeney Bicycle Light Sets are recalled because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. About 2,800 units are affected.

    Product
    Qumeney Bicycle Light Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26455·2026-04-30

    Travel size Afrin nasal spray lacks required child-resistant packaging

    Travel Size Afrin Original Nasal Spray 6 mL bottles are recalled because the packaging does not meet Poison Prevention Packaging Act requirements for imidazolines.

    Product
    Travel Size Afrin® Original Nasal Spray 6 mL Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26446·2026-04-30

    Segmart four-drawer dressers are unstable unless anchored to the wall

    Segmart 4-Drawer Dressers are recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children. About 16,440 units are affected.

    Product
    Segmart 4-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26457·2026-04-30

    Build-A-Bear Heartwarming Hugs bear pouch zipper sliders can detach

    Build-A-Bear Workshop Heartwarming Hugs Bears are recalled because the zipper slider on the side pouch can detach, posing a choking hazard to children. About 36,000 units are affected.

    Product
    Build-A-Bear Workshop Heartwarming Hugs Bears
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26447·2026-04-30

    Malker bicycle light sets let children access button cell batteries

    Malker Bicycle Light Sets are recalled because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. About 7,000 units are affected.

    Product
    Malker Bicycle Light Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26448·2026-04-30

    UHOMEPRO five-drawer dressers are unstable unless anchored to the wall

    UHOMEPRO 5-Drawer Dressers are recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children. About 5,190 units are affected.

    Product
    UHOMEPRO 5-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26449·2026-04-30

    Hepo adult portable bed rails pose entrapment and asphyxiation hazards

    Hepo adult portable bed rails are recalled because users can become entrapped within the rail or between the rail and the mattress. About 2,200 units are affected.

    Product
    Hepo Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26445·2026-04-30

    Kerosene heater fuel containers lack required flame mitigation devices

    1-K Kerosene Heater Fuel portable containers are recalled because they lack the flame mitigation devices required under the Portable Fuel Container Safety Act. About 30,155 units are affected.

    Product
    1-K Kerosene Heater Fluid Portable Fuel Containers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-04302026-01·2026-04-30

    Meat and Poultry Products with Recalled Dairy Ingredients

    USDA FSIS issued a public health alert for meat and poultry products containing FDA-regulated dairy ingredients that may be contaminated with Salmonella. No illnesses have been reported to date.

    Product
    FSIS Issues Public Health Alert for Various Meat and Poultry Products Containing FDA-Regulated Dairy Products That Have Been Recalled Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0497-2026·2026-04-29

    Sodium Chloride for Irrigation Lacks Sterility Assurance

    B. Braun Medical Inc. is recalling sodium chloride for irrigation solution (3000 mL bags) due to lack of assurance of sterility and potential leakage from the diaphragm port. Affected lots distributed nationwide have expiration dates through May 31, 2028.

    Product
    SODIUM CHLORIDE FOR IRRIGATION — SODIUM CHLORIDE FOR IRRIGATION (SODIUM CHLORIDE FOR IRRIGATION)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1890-2026·2026-04-29

    Medline Convenience Kits with 10mL Polycarbonate Colored Syringes Recalled

    Medline Industries is recalling multiple convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA 510(k) clearance. The recall affects approximately 270,311 units distributed in the US and internationally.

    Product
    Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ADD A ENDOVASCULAR PACK-LF DYNJ0429339L, DYNJ0429339M ANGIO ARTERIOGRAM PACK-LF DYNJ0774026K ANGIO KIT PACK DYNJ83746B ANGIO TRAY NO LIDO DYNJ85557A ANGIOGRAPHY PACK II DYNJ1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1892-2026·2026-04-29

    Medline Convenience Kits with Polycarbonate Syringes Recalled for Unapproved Design Changes

    Medline Industries is recalling Convenience Kits containing 10mL polycarbonate colored syringes because the products were modified in ways not approved by the FDA. The kits were distributed nationwide and internationally.

    Product
    Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ENSEMBLE GYNECO SCOPIE-LF DYNJ53744B LAVH GRH-LF DYNJ41792G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1842-2026·2026-04-29

    Medline Surgical Kits Recalled Due to Rescinded Regulatory Clearances

    Medline Industries is recalling 41 different surgical kit models nationwide because regulatory clearances for certain control syringes, guidewires, and high-pressure tubing have been rescinded. Affected facilities should stop use and contact Medline.

    Product
    Medline Kits: 1) NEWBORN ADMISSION, Model Number: DYKB1038; 2) DRAINAGE TRAY, Model Number: DYNDA3188; 3) VA ORLANDO SHOULDER PACK, Model Number: DYNJG001027B; 4) TUMESCENT SYRINGE KIT, Model Number: DYNJTUMSYR; 5) OMC PTCA PACK, Model Number: DYNJT3719; 6) PORT PACK,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1886-2026·2026-04-29

    Medline Polycarbonate Syringes Recalled for Unapproved Design Changes

    Medline Industries is recalling select Convenience Kits containing 10mL polycarbonate colored syringes (Eye Pack and Heart Cath Pack) due to unapproved design changes made outside of FDA 510(k) clearance.

    Product
    Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes EYE PACK DYNJ35056A HEART CATH PACK DYNJ69318A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1834-2026·2026-04-29

    Medline angiography and catheter kits subject to rescinded regulatory clearances

    Medline Industries is recalling 12 types of angiography and catheter kits because their 510(k) regulatory clearances have been rescinded. The kits were distributed nationwide.

    Product
    Medline Kits: 1) ANGIOGRAPHY PACK-LF, Model Number: DYNJQ0505M; 2) ANGIO PACK, Model Number: DYNJT2021G; 3) ANGIOGRAPHY PACK, Model Number: DYNJ31377B; 4) ANGIO PACK, Model Number: DYNJ51279; 5) ANGIOGRAPHY PACK II, Model Number: DYNJ52447; 6) CATH ANGIO PACK, Model Nu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0666-2026·2026-04-29

    Salute Seasonings ground allspice may be contaminated with Salmonella

    Salute Seasonings Ground All Spice is being recalled because the product may be contaminated with Salmonella. The action covers 330 units across three lots.

    Product
    SALUTE SEASONINGS; Ground All Spice; Net Wt 16oz; Unistel Industries 650 Blossom Road Rochester, NY 14610; UPC: 7 69203 01617 0
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0495-2026·2026-04-29

    Sterile Water for Injection bags recalled due to sterility concerns

    B. Braun Medical Inc. is recalling Sterile Water for Injection USP 3000 mL bags (24,928 units) distributed nationwide due to lack of assurance of sterility and potential leakage from the diaphragm port.

    Product
    STERILE WATER — STERILE WATER (WATER)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1843-2026·2026-04-29

    Control Syringes and Related Devices FDA Regulatory Clearances Rescinded

    Medline Industries has recalled Control Syringes (Model DNSC89369 and DYNJSYR10C), Guidewires, and High-Pressure Tubing after their FDA 510(k) regulatory clearances were rescinded. The devices were distributed nationwide.

    Product
    Medline Kits: 1) SYR CONTROL 8ML ROTATING, Model Number: DNSC89369; 2) SYRINGE 10ML CONTROL MLL, Model Number: DYNJSYR10C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1879-2026·2026-04-29

    Medline Convenience Kits with Syringes Recalled for Unapproved Design Changes

    Medline Industries, LP is recalling Medline Convenience Kits containing 10mL Polycarbonate Colored Syringes due to unapproved design changes made outside of FDA 510(k) clearance. The recall affects approximately 270,311 units distributed worldwide.

    Product
    Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BIOPSY PACK DYNJ38587A, DYNJ38587B BIOPSY/DRAINAGE TRAY-LF DYNJ30078D W LINQ PACK DYNJ59108B
    Category
    Medical Device
    Distribution
    Distributed nationwide