The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

1326–1350 of 32253

  • SevereFDA (Food)·H-0511-2026·2026-02-25

    IKM Aluminum Saucepan Recalled Over Lead Contamination Risk

    Lotus Mom Corporation is recalling 56 units of the IKM Aluminum Saucepan 9" with Wooden Handle due to potential leachable lead contamination. The product was distributed in California and Colorado.

    Product
    IKM Aluminum Saucepan 9" with Wooden Handle. Sticker label: ALUMINIUM PAN 2 SIDE POUTED WOODEN HANDLE 9" UPC 7 023672 411878 US $ 17.99 Sticker label: IKM INDIAN KITCHEN MART
    Category
    Consumer Product
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1415-2026·2026-02-25

    Medline Recalls Surgical Convenience Kits Over Sterilization Calibration Issues

    Medline is recalling 12,418 units of various surgical convenience kits due to calibration issues with equipment used for sterilization and packaging, which may affect the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) ROBOTIC GYN CDS-1, Model Number: CDS982893I; 2) GYN LAPAROSCOPY CDS, Model Number: CDS983300J; 3) NHP ROBOTIC GYNE CDS, Model Number: CDS984243G; 4) ROBOTIC-LF, Model Number: CDS984543D; 5) ROBOTIC-LF, Model Number: CDS984543F; 6)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0516-2026·2026-02-25

    Frozen Cooked Shrimp Recalled Over Cesium-137 Contamination Risk

    H & N Group Inc. is recalling frozen cooked medium shrimp due to potential contamination with Cesium-137 from manufacturing under insanitary conditions. The product was distributed to approximately 30 retail locations in the greater Houston and Gulf Coast areas.

    Product
    Frozen Cooked Medium Shrimp Peeled & Deveined, Tail Off-White Shrimp; 1 lbs retail plastic bag. UPC: 041220333035
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1397-2026·2026-02-25

    Medline Sterile Surgical Kits Recalled Over Sterilization Equipment Calibration

    Medline is recalling 4,757 units of convenience surgical kits distributed worldwide due to calibration issues with sterilization and packaging equipment that may affect sterility assurance.

    Product
    Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS, Model Number: ACC010499; 2) KIT UROLOGY URETHROPLASTY, Model Number: DYKMBNDL117C; 3) KIT PLASTIC INSERT TISSUE EXPA, Model Number: DYKMBNDL158; 4) KIT PLASTIC ABDOMINOPLASTY, Model Number: DYKMBNDL170; 5) KIT…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1387-2026·2026-02-25

    Medline Nerve Block Trays Recalled Over Sterilization Calibration Issues

    Medline is recalling 448 units of its BASIC NERVE BLOCK TRAY W/LINEN (Model PAIN0150C) due to calibration issues with sterilization and packaging equipment that could affect the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) BASIC NERVE BLOCK TRAY W/LINEN, Model Number: PAIN0150C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1414-2026·2026-02-25

    Medline Labor and Delivery Convenience Kits Recalled Over Sterilization Calibration

    Medline is recalling 27,320 labor and delivery convenience kits due to calibration issues with sterilization equipment that may affect the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) OB KIT, Model Number: DYKM2326; 2) KIT LABOR DELIVERY TUBAL LIGAT, Model Number: DYKMBNDL165; 3) KIT LABOR & DELIVERY D&C/D&E, Model Number: DYKMBNDL31; 4) KIT LABOR & DELIVERY CERCLAGE, Model Number: DYKMBNDL38; 5) L & D PACK-LF, Model…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1371-2026·2026-02-25

    Olympus Thunderbeat Surgical Device Recall Due to Adverse Events

    Olympus is recalling 9,542 Thunderbeat surgical devices worldwide due to continued reports of adverse events. The recall affects all lots of the TB-0545FCS model.

    Product
    Olympus Thunderbeat 5 mm, 45 cm, Front-Actuated Grip Type S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1382-2026·2026-02-25

    Olympus Thunderbeat Surgical Device Recall Over Adverse Events

    Olympus is recalling 1,538 Thunderbeat 5 mm surgical devices worldwide due to continued reports of adverse events. The recall affects all units of Model No. TB-0510IC.

    Product
    Olympus Thunderbeat 5 mm, 10 cm, Inline Grip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1362-2026·2026-02-25

    Wilson-Cook Medical Recalls Teslatome Bipolar Sphincterotomes Over Current Path Risk

    Wilson-Cook Medical Inc. is recalling 153 Teslatome Bipolar Sphincterotomes due to a potential void in the material separating the wire guide and cutting wire lumens, which may cause an inappropriate path of current during cutting.

    Product
    Teslatome Bipolar Sphincterotomes REF: TESLA-B2535-260 Model Number: G60784 UDI-DI code: 00827002607842 REF: TESLA-B2535-450 Model Number: G60785 UDI-DI code: 00827002607859 These devices are used for cannulation of the ductal system and for sphincterotomy. If…
    Category
    Medical Device
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1352-2026·2026-02-25

    Olympus High Flow Insufflation Unit Recalled Due to Software Algorithm Issue

    Olympus Corporation of the Americas is recalling the Olympus High Flow Insufflation Unit (Model UHI) because a software algorithm issue may cause overpressure events.

    Product
    Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of the abdominal cavity, and automatic suction and smoke evacuation to facilitate laparoscopic observation and treatment within the abdominal cavity.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V108000·2026-02-24

    Newmar motorhome hood stop adhesive may fail allowing detachment in transit

    Newmar is recalling certain 2018-2026 Bay Star and Bay Star Sport motorhomes because the hood stops mounting adhesive may fail, allowing the hood stop to detach while the vehicle is in transit.

    Product
    NEWMAR — NEWMAR BAY STAR SPORT, BAY STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V105000·2026-02-23

    Kia Telluride front seat back frames may not restrain occupants

    Kia is recalling certain 2025 Telluride vehicles with power front seats because a manufacturing error may leave the driver and passenger seat back frame assemblies unable to properly restrain occupants in a crash.

    Product
    KIA — KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V106000·2026-02-23

    Subaru Recalls 2025-2026 Hybrid Vehicles for Fuel Cap Seal Defect

    Subaru is recalling 2025 Forester and 2026 Crosstrek hybrids because a faulty fuel cap seal may cause fuel to spill when the tank is near full and temperatures rise.

    Product
    SUBARU — SUBARU CROSSTREK HYBRID, FORESTER HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·006-2026·2026-02-22

    Rosina Recalls Frozen Meatballs Due To Possible Metal Contamination

    Rosina Food Products is recalling approximately 9,462 pounds of frozen Bremer meatballs due to possible metal contamination. The products were distributed to Aldi locations nationwide.

    Product
    Rosina Food Products, Inc. — Rosina Food Products, Inc. Recalls Ready-To-Eat Frozen Meatball Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V098000·2026-02-20

    Demers Ambulances Recall FXP174 Models for Seat Floor Strength Defect

    Braun Industries is recalling 2025-2026 Demers FXP174 ambulances because the floor may not securely hold seats during a crash, increasing injury risk.

    Product
    Demers Ambulances — Demers Ambulances FXP174
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V103000·2026-02-20

    Volvo EX30 high voltage battery may short circuit and overheat

    Volvo is recalling certain 2025 EX30 vehicles because the high voltage battery may experience a short circuit and overheat. Owners are advised to limit charging to a maximum of 70%.

    Product
    VOLVO — VOLVO EX30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V100000·2026-02-20

    Rossmonster Recalls 2023-2025 Baja Motorhomes Due to Brake Line Routing

    Rossmonster is recalling 2023-2025 Baja Ex and Baja LX motorhomes because incorrectly routed front brake lines may contact tires, causing leaks and reduced braking performance.

    Product
    ROSSMONSTER — ROSSMONSTER BAJA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·004-2026·2026-02-19

    Sobico USA Recalls Frozen Siluriformes Fish Imported Without Reinspection

    Sobico USA LLC is recalling approximately 13,464 pounds of frozen, raw Siluriformes fish products imported from Vietnam without the benefit of import reinspection.

    Product
    Sobico USA LLC Recalls Siluriformes Fish Products Imported Without The Benefit of Import Reinspection
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·26V097000·2026-02-19

    Range Rover panoramic sunroof side trim may not be properly secured

    Land Rover is recalling certain 2023-2026 Range Rover and Range Rover Sport vehicles because the panoramic sunroof side finisher trim may not be properly secured and can detach.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V096000·2026-02-19

    BMW Recalls Multiple Models for Air Conditioning Wiring Fire Risk

    BMW is recalling specific 2023-2026 models because the air conditioning wiring harness may be damaged during filter replacement, increasing the risk of a fire.

    Product
    BMW — BMW I7 EDRIVE50, I7 XDRIVE60, I5 EDRIVE40, I5 XDRIVE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·005-2026·2026-02-19

    Ajinomoto Recalls Frozen Chicken Fried Rice Due to Glass Contamination

    Ajinomoto Foods North America is recalling frozen chicken fried rice products due to possible glass contamination. No injuries have been reported.

    Product
    Ajinomoto Foods North America — Ajinomoto Foods North America, Inc. Recalls Chicken Fried Rice Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V093000·2026-02-17

    Prevost Recalls 2025-2026 X3-45 Buses Due to Seat Anchor Defect

    Prevost is recalling 2025-2026 X3-45 commuter buses because improperly installed seat anchors may not restrain occupants during a crash.

    Product
    PREVOST — PREVOST X3-45 COMMUTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V089000·2026-02-17

    Winnebago View and Navion rear roof cap trim may detach

    Winnebago is recalling certain 2020-2023 View and Navion recreational vehicles because the rear roof cap aerofence trim may become loose and detach during transit.

    Product
    WINNEBAGO — WINNEBAGO NAVION, VIEW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V090000·2026-02-17

    Ford Recalls 2025 Transit Vehicles for Brake Pedal Disconnection Risk

    Ford is recalling 2025 Transit vehicles because the brake pedal may disconnect from the booster pushrod, causing a loss of brake function and increasing crash risk.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide