The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

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.

24826–24850 of 50443

  • HighFDA (Devices)·Z-2552-2019·2019-10-02

    Sentinel CH SpA Recalls Alinity c Lithium Reagent Kits

    Sentinel CH SpA is recalling Alinity c Lithium Reagent Kits due to a potential carryover issue that may result in falsely elevated lithium patient results.

    Product
    Alinity c Lithium Reagent Kit- intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 08P5320
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V697000·2019-10-02

    BMW Recalls 2020 S1000 RR Motorcycles Due to Oil Cooler Hose Defect

    BMW is recalling 416 2020 S1000 RR motorcycles because oil cooler hoses may not be attached properly, potentially causing an oil leak that increases crash risk.

    Product
    BMW — BMW S1000 RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2561-2019·2019-10-02

    Elekta Monaco RTP System Recalled for Potential Dose Calculation Errors

    Elekta Inc is recalling 49 Monaco RTP Systems because unintentional changes to electron density settings may cause incorrect dose calculations for radiation therapy plans.

    Product
    Monaco RTP System, 5.50/5.51, radiation treatment planning system Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for external beam radiation therapy. The system calculates dose for photon, electron, and carbon treatment plans…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2756-2019·2019-10-02

    Medline Electric Surgical Clipper Recalled for Overheating Charger Base

    Medline Industries is recalling 500 electric surgical clippers because a defective circuit board component may cause the charger base to overheat and malfunction.

    Product
    MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE, REF DYND70800 Product Usage: Medline Surgical Clipper is intended for the removal of body hair from the patient as required prior to surgery or other minor procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V695000·2019-10-02

    Daimler Recalls 2018-2019 Sprinter Vehicles for Inactive Airbag Systems

    Daimler Vans USA is recalling 2018-2019 Mercedes-Benz and Freightliner Sprinter vans because their airbag systems may not have been activated, increasing crash injury risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 4500, SPRINTER 1500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V693000·2019-10-02

    Mercedes-Benz Recalls 2018-2019 Sprinter and Metris Vans for Safety Inspection

    Daimler Vans USA is recalling 2018-2019 Mercedes-Benz Sprinter and Metris vans because they left the reassembly plant without final quality inspection of safety-relevant parts.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS, SPRINTER 3500, SPRINTER 4500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2560-2019·2019-10-02

    Elekta Monaco RTP System Recalled for Potential Dose Calculation Errors

    Elekta Inc is recalling 30 units of the Monaco RTP System 5.40 Unity because unintentional changes to electron density settings may result in incorrect dose calculations for radiation treatment plans.

    Product
    Monaco RTP System, 5.40 Unity, radiation treatment planning system Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for external beam radiation therapy. The system calculates dose for photon, electron, and carbon treatment…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2247-2019·2019-10-02

    H-E-B Strawberry Ice Cream Recalled for Potential Metal Shavings

    H-E-B is recalling 404 units of Select Ingredients Creamy Creations Strawberry Ice Cream in Texas due to potential metal shavings.

    Product
    H-E-B Select Ingredients Creamy Creations Strawberry Ice Cream 1/2 gallon UPC 4122034602 packaged in paper carton with lid
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0034-2020·2019-10-02

    Star Fisheries Recalls Fresh Irish Salmon Fillets for Listeria Risk

    Star Fisheries, Inc. is recalling fresh Irish salmon fillets due to potential Listeria monocytogenes contamination. The product was distributed to retail stores in California.

    Product
    Irish Salmon Organic Atl HON; 55 lb. cases received. Fresh Irish Salmon Fillet Ireland Farmed. Random weight boxes fillets cut and distributed. Keep Refrigerated, Color Added. Packed by Star Fisheries Inc., Wilmington, CA
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·19V690000·2019-10-01

    Jayco Recalls 2019-2020 Redhawk SE Motorhomes for Seatbelt Warning Defect

    Jayco is recalling 2019-2020 Redhawk SE motorhomes because the seatbelt-unfastened warning light may not illuminate for five seconds after ignition, increasing crash injury risk.

    Product
    JAYCO — JAYCO REDHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V687000·2019-09-30

    Ford Recalls 2020 Explorers for Wiring Harness Fire Risk

    Ford is recalling 2020 Explorers because a wiring harness may contact the A/C pulley, causing a short circuit and increasing fire risk.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V682000·2019-09-27

    Jaguar Recalls 2019-2020 F-Type Vehicles for Incorrect Tire Placard Label

    Jaguar is recalling 2019-2020 F-Type vehicles with 18-inch rear wheels because the tire placard label lists an incorrect tire size, which could lead to improper tire installation.

    Product
    JAGUAR — JAGUAR F-TYPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V686000·2019-09-27

    Daimler Recalls 2017-2020 Saf-T-Liner C2 School Buses for Loose Fasteners

    Daimler Trucks North America is recalling 618 school buses because loose torque converter fasteners could cause the vehicle to become disabled in traffic, increasing injury risk during evacuation.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19211·2019-09-26

    DeWALT Recalls Utility Bars Due to Injury Hazard

    DeWALT is recalling 40-inch utility bars that can break while prying, posing an injury hazard to users.

    Product
    DeWALT Multi-Functional Utility Bars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19210·2019-09-26

    ASKO Recalls Dishwashers Due to Power Cord Fire Hazard

    ASKO is recalling about 26,600 dishwashers because the power cord can overheat, posing a fire hazard. No injuries or property damage have been reported.

    Product
    ASKO dishwashers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2231-2019·2019-09-25

    Ore Ida Spud Bites Recalled Due to Hard Foreign Material Presence

    McCain Foods USA is recalling Ore Ida Spud Bites because they may contain hard foreign material. The product was distributed to foodservice wholesalers and restaurant distribution centers.

    Product
    Ore Ida Spud Bites, packaged in 5lb. plain poly foodservice bags, six bags per case, frozen, Case UPC: 1 00 72714 00093 2. SKU: OIF00093A
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-2232-2019·2019-09-25

    Stavis Seafoods Recalls MiCal Yellowfin Tuna Poke Cubes Due to Histamine

    Stavis Seafoods, Inc. is recalling MiCal brand Yellowfin Tuna Poke Cubes because the product may contain elevated levels of histamine.

    Product
    MiCal brand YELLOWFIN TUNA POKE CUBE, Raw, Frozen, Product of Vietnam, Wild Caught. Cube size - 1 inch (2cm x 2cm) AAA grade. Product is packed in 1lb vacuum packed bags in a pre-printed labeled master case. Master case weight is 5lbs.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-2541-2019·2019-09-25

    Wilson-Cook Recalls Hemospray Endoscopic Hemostat Due to Misassembly

    Wilson-Cook Medical Inc. is recalling 160 units of Hemospray Endoscopic Hemostat because misassembly may prevent the device from spraying powder.

    Product
    Hemospray Endoscopic Hemostat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2149-2019·2019-09-25

    Maquet Cardiopulmonary Sets Recalled Due to Incorrect Quick Connector Assembly

    Maquet is recalling 54 cardiopulmonary sets because quick connectors were assembled in reverse, preventing proper priming and function.

    Product
    Maquet Cardiopulmonary (MCP)/Getinge HLS Set Advanced 7.0. Model Number BEQ-HLS-7050 USA, Part Number 701052794
    Category
    Medical Device
    Distribution
    17 states
  • HighNHTSA·19V679000·2019-09-25

    Volkswagen Recalls Multiple Models Due to Regulatory Non-Compliance

    Volkswagen is recalling specific 2007-2019 models because internal evaluation modifications may cause non-compliance with regulatory requirements, potentially increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN, PASSAT, JETTA HYBRID, BEETLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2544-2019·2019-09-25

    Ad-Tech Drill Sleeve Guides Recalled for Potential Drill Bit Seizure

    Ad-Tech Medical Instrument Corporation is recalling specific Drill Sleeve Guides because the inner diameter was under tolerance, which could cause the drill bit to seize during surgery.

    Product
    AD-TECH Drill Sleeve Guides, used with Ad-Tech Placement Kits: (a) REF DSG-90-2.3N (b) REF DSG-6.3-090-2.4N
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Food)·F-2158-2019·2019-09-25

    House of Spices India Recalls MDH Sambar Masala for Salmonella

    House of Spices India, Inc. is recalling MDH Sambar Masala spice boxes because the product tested positive for Salmonella upon arrival in the United States.

    Product
    MDH Sambar Masala; Spices blend for South Indian Cuisine 3.5 oz. (100 g) box. code 6291103750327 Ingredients: coriander, Chili Rec, Cumin Powder, Tumeric, Salt White, Fenugreek seeds, Mustard, Lentil (Chana Dal) Lentil (Pigeon peas lentil) Black Pepper, Fennel, Cassia…
    Category
    Food
    Distribution
    1 state