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.

20551–20575 of 50413

  • HighFDA (Devices)·Z-1514-2021·2021-05-05

    Donjoy Ultrasling Pro AB Arm Sling Recalled for Failed Rivet

    DJ Orthopedics is recalling Donjoy Ultrasling Pro AB arm slings due to a failed rivet at the chafe tab.

    Product
    DONJOY REF:11-0473-9 ULTRASLING PRO AB, UNIVERSAL, Rx ONLY, UDI: (01)00190446683681 - Product Usage: intended for medical purposes to immobilize the arm, by means of a fabric band suspended from around the neck.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V314000·2021-05-04

    Arcimoto Motorcycles Recalled for Defective Seat Belt Retractors

    Arcimoto is recalling certain 2019-2021 motorcycles because the seat belt retractor spool sleeve may crack, preventing the belt from retracting. This increases the risk of injury. Owners should contact Arcimoto for free replacement.

    Product
    ARCIMOTO — ARCIMOTO FUV, DELIVERATOR, RAPID RESPONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V311000·2021-05-04

    Arcimoto Electric Vehicles Recalled: Inverter Software Error Causes Battery Shutdown Risk

    Arcimoto is recalling 2019-2021 FUV, 2020 Deliverator, 2020-2021 Roadster, and 2021 Rapid Responder vehicles due to a software error that may cause unexpected battery shutdown, increasing crash risk. Owners should contact Arcimoto or NHTSA for remedy details.

    Product
    ARCIMOTO — ARCIMOTO FUV, DELIVERATOR, RAPID RESPONDER, ROADSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V312000·2021-05-04

    Blue Bird Recalls 2018-2022 All American Buses Due to Fuel Leak Risk

    Blue Bird is recalling 2018-2022 All American buses because a fuel rail leak could cause a fire. Owners should contact customer service for updates.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V310000·2021-05-04

    2021 Jeep Cherokee Transmission Oil Cooler Hose May Leak and Cause Fire

    Chrysler is recalling certain 2021 Jeep Cherokee vehicles because the transmission oil cooler hose may have been incorrectly cured, allowing transmission fluid to leak and increasing the risk of fire. Dealers will inspect and replace the hose for free.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·016-2021·2021-05-01

    Hempstead Foodservice Recalls Pork Chops for Undeclared Soy Allergen

    Hempstead Foodservice is recalling pork chops because they contain undeclared hydrolyzed soy protein, a known allergen.

    Product
    Hempstead Foodservice Inc. — Hempstead Foodservice Recalls Pork Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·21V304000·2021-04-30

    KTM Recalls 790 Adventure Motorcycles Due to Weak Front Brake Spring

    KTM is recalling 2019-2020 790 Adventure models because a weak front brake spring may reduce braking functionality, increasing the risk of a crash.

    Product
    KTM — KTM 790 ADVENTURE, 790 ADVENTURE R, 790 ADVENTURE R RALLY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V306000·2021-04-30

    Tiffin Bus and Phaeton motorhomes recalled for fuel rail leakage and fire risk

    Tiffin Motorhomes is recalling 2017-2021 Bus and Phaeton vehicles due to fuel rail assembly defects that may leak, posing a fire risk. Owners should contact Tiffin customer service at 1-256-356-8661 for a free inspection.

    Product
    TIFFIN — TIFFIN BUS, PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V305000·2021-04-30

    NorthStar Ambulance Recall for Display Lockup Hazard

    Braun Northwest is recalling 2013-2020 NorthStar Ambulances because LCD displays may lock up, potentially delaying emergency efforts.

    Product
    NORTHSTAR — NORTHSTAR AMBULANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21740·2021-04-29

    Modernist Pantry Recalls Sodium Hydroxide for Packaging and Labeling Defects

    Modernist Pantry is recalling Kitchen Alchemy Sodium Hydroxide products because the packaging is not child-resistant and labels violate federal hazardous substance requirements.

    Product
    Modernist Pantry Kitchen Alchemy Sodium Hydroxide
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21E037000·2021-04-29

    Full Vision Recalls Rogers Brothers Rear Impact Guards Due to Weak Steel

    Full Vision is recalling Rogers Brothers Rear Impact Guards because the steel may not meet specifications, potentially reducing strength and increasing injury risk in crashes.

    Product
    STRUCTURE:BODY:BUMPERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1477-2021·2021-04-28

    Smiths Medical Recalls Stopcock Rotators Due to Incomplete Welds

    Smiths Medical ASD Inc. is recalling specific stopcock rotator components used in cardiac kits due to insufficient or incomplete welds.

    Product
    Stopcock rotator (Component): a. 1050 STOPCOCK ROTATOR, OFF HANDLE, Model Number MX1431MR b. 1050 STOPCOCK LEFT ROTATOR, OFF HANDLE, Model Number MX1431MRL c. 700 PSI STPCK W/ ROTATOR, Model Number MX4331R. Stopcocks and manifolds used to control the direction of IV fluid…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0451-2021·2021-04-28

    Trader Joe's White Corn Tortilla Chips Recalled for Undeclared Milk

    Snak King Corporation is recalling Trader Joe's Restaurant Style White Corn Tortilla Chips because they may contain undeclared milk.

    Product
    Trader Joe's Restaurant Style White Corn Tortilla Chips; Net Wt. 9 oz. (255g)
    Category
    Food
    Distribution
    23 states
  • HighFDA (Devices)·Z-1452-2021·2021-04-28

    Biotronik ITREVIA 7 Defibrillators Recalled for Premature Battery Depletion

    Biotronik is recalling 670 ITREVIA 7 defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.

    Product
    BIOTRONIK ITREVIA 7, VR-T DF-4, REF 393041, UDI: 04035479129569 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1463-2021·2021-04-28

    Biotronik Intica Neo 7 VR-T DX DF-1 ProMRI Recall for Battery Depletion

    Biotronik is recalling 17 Intica Neo 7 VR-T DX DF-1 ProMRI implantable cardioverter defibrillators due to a potential for premature battery depletion.

    Product
    BIOTRONIK INTICA NEO 7 VR-T DX DF-1 ProMRI, REF 429559, UDI: 04035479156855 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1447-2021·2021-04-28

    Biotronik Iforia 7 ICDs Recalled for Premature Battery Depletion

    Biotronik Inc is recalling 1,176 Iforia 7 implantable cardioverter defibrillators due to a potential for premature battery depletion.

    Product
    BIOTRONIK Iforia 7, vr-T, DX, DF-1,REF 390090, UDI: 04035479127176 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0437-2021·2021-04-28

    Avanti Recalls 365 Whole Foods Market Farm Raised Cooked Shrimp

    Avanti Frozen Foods is recalling 365 Whole Foods Market Farm Raised Cooked Shrimp because uncooked shrimp were inadvertently packaged as cooked.

    Product
    365 Whole Foods Market Farm Raised Cooked Shrimp 2 lbs/Ready- to - Serve Tail-On/Peeled & Deveined/41-55 Shrimp/lb NET WT 32 OZ (2 LB) 907g packaged in clear plastic bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1443-2021·2021-04-28

    Biotronik Ilestro 7 VR-T Defibrillators Recalled for Premature Battery Depletion

    Biotronik Inc is recalling 1,000 Ilestro 7 VR-T implantable defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.

    Product
    BIOTRONIK Ilestro 7 VR-T, DF-1, REF 383578, UDI: 04035479125349 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0454-2021·2021-04-28

    Reser's Macaroni Salad Recalled for Undeclared Wheat and Egg Allergens

    Reser's Fine Foods is recalling Freshness Guaranteed Macaroni Salad Amish because the bottom label incorrectly identifies the product as Red Potatoes or Baked Beans, failing to declare wheat and egg allergens.

    Product
    Freshness Guaranteed Macaroni Salad Amish, item # 579284, refrigerated, packaged in a clear cup with clear snap on lid, net wt. 32 oz. UPC 0 78742 13235 8. Each master case containing 6/32 oz. packages. Distributed by: Walmart Inc, Bentonville, AR. The CORRECT label is read…
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1475-2021·2021-04-28

    Smiths Medical Recalls Medex High Pressure Adaptors and LogiCal Kits

    Smiths Medical is recalling specific lots of Medex High Pressure Adaptors and LogiCal Kits due to potential manufacturing defects in welds.

    Product
    ANGIOGRAPHIC KIT W/MX123-3MR MANIFOLD, Model Number MX1030. for use during angiography and other special procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1442-2021·2021-04-28

    Biotronik Ilestro 7 DR-T Recall for Premature Battery Depletion

    Biotronik is recalling Ilestro 7 DR-T implantable defibrillators due to a potential for premature battery depletion. Affected devices are distributed nationwide and worldwide.

    Product
    BIOTRONIK Ilestro 7 DR-T, DF-4, REF383564, UDI: 04035479125202 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V301000·2021-04-28

    Multiple Hyundai models recalled for engine piston ring defect

    Hyundai is recalling 2019–2021 Kona, Elantra, and Veloster models with 2.0L engines. Improperly heat-treated piston rings may cause engine damage, stalling, and fire risk.

    Product
    HYUNDAI — HYUNDAI ELANTRA, VELOSTER, KONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1453-2021·2021-04-28

    BIOTRONIK IPERIA 7 ICDs Recalled for Premature Battery Depletion

    BIOTRONIK Inc is recalling 2,881 IPERIA 7 ICDs and CRT-Ds due to a potential for premature battery depletion.

    Product
    BIOTRONIK IPERIA 7, DR-T DF4 ProMRI, REF 392423, UDI: 04035479128913 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
    Category
    Medical Device
    Distribution
    Distributed nationwide