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.

3751–3775 of 52939

  • HighFDA (Food)·H-0522-2025·2025-08-27

    Chick-fil-A biscuit mix recalled for undeclared eggs in bulk bags

    Biscuit Mix packed exclusively for Chick-fil-A, Inc. in 2.625 lb bags is recalled for undeclared eggs. The recall covers 150 cases of 12 bags.

    Product
    BISCUIT MIX, SNG 1000042143 NET WEIGHT 2.625 LBS Packed Exclusively For: Chick-fil-A, Inc. 5200 Buffington Road Atlanta, Ga 30349
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0503-2025·2025-08-27

    Bulk raw ramen noodles recalled because soy lecithin source is undeclared

    Raw Ramen Noodle HA #22W (4942) in 10 lb bulk cases, made by Kobayashi Noodle USA, is recalled because the label does not declare soy as the source of the lecithin ingredient. 2,800 cases are affected.

    Product
    Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noodle HA #22W (4942) UPC: NONE Manufactured by: Kobayashi Noodle USA Allergens: Wheat, Egg
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0502-2025·2025-08-27

    Raw ramen noodles recalled because label omits soy as lecithin source

    Raw Ramen Noodle HA #22W in 10 lb bulk cases, made by Kobayashi Noodle USA, is recalled because the label does not declare soy as the source of the lecithin ingredient. 945 cases are affected.

    Product
    Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noodle HA #22W (16049) UPC: NONE Manufactured by: Kobayashi Noodle USA Allergens: Wheat, Egg
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0505-2025·2025-08-27

    Ojasvita Chocomalt 200 g pouches recalled for undeclared soy lecithin

    Sri Sri Tattva Ojasvita Chocomalt, 7 oz / 200 g paper pouches, is recalled because it contains undeclared soy lecithin. 1,100 units are affected.

    Product
    Sri Sri Tattva, Ojasvita Chocomalt,7oz / 200g, Paper Pouch, 25 packages per case
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·H-0504-2025·2025-08-27

    Zero sugar soda cans recalled because they contain full sugar product

    7up Zero Sugar Tropical Soda in 12 fl oz cans is recalled because the cans are labeled Zero Sugar but contain full sugar product. 1,954 cases are affected.

    Product
    7up Zero Sugar Tropical Soda, 12 FL OZ (355 mL) aluminum cans, packaged in 12 pack cardboard cartons labeled as 7up Tropical Flavored Soda, UPC (on can): 078000037975, UPC (on carton): 078000037982
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0520-2025·2025-08-27

    Frozen half shell oysters recalled over potential norovirus contamination

    Imported Frozen Half Shell Oysters in 15-pound boxes, lot B250123, are recalled because they are potentially contaminated with norovirus. 828 cartons are affected.

    Product
    Product is Frozen Half Shell Oysters in 15 pound blacks. Packaged in generic brown cardboard boxes. Side panel reads: HAFL SHELL OYSTER Spec: 144PCS; Imported by: Khee Trading Inc., Compton, CA Side panel reads: Method of harvest: Farm Raised Country of Origin: Republic of Korea
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·H-0521-2025·2025-08-27

    Frozen half shell oysters from lot B250112 recalled over norovirus risk

    Imported Frozen Half Shell Oysters in 15-pound boxes, lot B250112, are recalled because they are potentially contaminated with norovirus. 98 cartons are affected.

    Product
    Product is Frozen Half Shell Oysters in 15 pound blacks. Packaged in generic brown cardboard boxes. Side panel reads: HAFL SHELL OYSTER Spec: 144PCS; Imported by: Khee Trading Inc., Compton, CA Side panel reads: Method of harvest: Farm Raised Country of Origin: Republic of Korea
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2329-2025·2025-08-27

    Endoscopy video processors recalled over hot light guide and thermal injury risk

    Pentax Medical EPK-i8020c video processors are recalled after reports of darkened images, smoke-like steam and a hot endoscope light guide that may cause thermal injury to the patient's mucous membrane. 144 units are affected.

    Product
    Pentax Medical Video Processor; Model Number: EPK-i8020c;
    Category
    Medical Device
    Distribution
    20 states
  • HighFDA (Devices)·Z-2344-2025·2025-08-27

    OtoLase starter kits recalled over potentially unsterilized product labeled as sterile

    OtoLase Starter Kits, UPN AC-2003748, batches 32644549 and 32769567, are recalled because finished product labeled as sterile may not have been sterilized. 13 units are affected.

    Product
    OtoLase Starter Kit; UPN: AC-2003748. Indicated for a variety of surgical uses including ablation, coagulation, incision, excision, and vaporization of soft tissue.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-2338-2025·2025-08-27

    Electrosurgical generators recalled over system error causing reboots during use

    The ESG-410 Electrosurgical Generator is recalled because it may display an E0662 System Error followed by a single automatic reboot or a continuous reboot loop. 155 units are affected.

    Product
    Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator ESG-410 Surgical Energy Platform (SEP). Model Number: WA91327U. The ESG-410 Electrosurgical Generator is an electrosurgical generator which utilizes monopolar and bipolar high frequency current
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2339-2025·2025-08-27

    Legacy electrosurgical generators recalled over system error triggering repeated device reboots

    The ESG-410 Legacy Electrosurgical Generator, model WA91307C, is recalled because it may display an E0662 System Error followed by a single automatic reboot or a continuous reboot loop. 434 units are affected.

    Product
    Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator ESG-410. Model Number: WA91307C. The ESG-410 Electrosurgical Generator is an electrosurgical generator which utilizes monopolar and bipolar high frequency current and supports ultrasonic instr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0590-2025·2025-08-27

    Epinephrine injection vials recalled for lack of assurance of sterility

    Hospira Epinephrine Injection USP, 1 mg/10 mL, lots LY3681, LY4360 and LY4416, is recalled nationwide for lack of assurance of sterility. 49,620 vials are affected.

    Product
    Vial Label: Epinephrine Injection, USP, 1mg/10mL (0.1 mg/mL), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045, USA. NDC 0409-4933-05. Case: NDC 0409-4933-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2336-2025·2025-08-27

    Estrone diagnostic kits recalled over rare falsely high or low results

    Estrone RIA kits, catalog number DSL8700, are recalled because certain lots may rarely give falsely high or falsely low patient results. 279 units are affected.

    Product
    Estrone RIA Catalog Number DSL8700 UDI Code: 15099590211615 Estrone RIA is an in vitro diagnostic manual medical device used by healthcare professionals for the quantitative measurement of estrone in human serum and plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2340-2025·2025-08-27

    Deep brain stimulation burr hole kits recalled over retaining clip closing resistance

    Burr Hole Cover Kits used with the Vercise Deep Brain Stimulation System are recalled because resistance closing the retaining clip may cause procedural delay or lead migration requiring further surgery. 24,583 units are affected.

    Product
    Burr Hole Cover Kit, REF: M365DB4600C0; Burr Hole Cover Spares Kit, REF: M365DB4605C0. Components of Vercise Deep Stimulation System used with the Surgical Implant Manual
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25E052000·2025-08-26

    Chrysler Recalls Mopar Rearview Camera Modules Due to Image Display Issues

    Chrysler is recalling specific Mopar rearview camera modules because cracks in the microprocessor may prevent the image from displaying properly, increasing crash risk.

    Product
    BACK OVER PREVENTION: SENSING SYSTEM: CAMERA recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V554000·2025-08-26

    Tiffin Recalls 2025 GT1 Vans Due to Short Rear Seat Belts

    Tiffin Motorhomes is recalling 2025 GT1 Touring vans because rear seat belt buckles may be too short to fasten, increasing injury risk in a crash.

    Product
    TIFFIN — TIFFIN GT1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V552000·2025-08-26

    Ram ProMaster and Dodge Journey rearview cameras may not display properly

    Chrysler is recalling certain 2019-2021 Ram ProMaster and 2019-2020 Dodge Journey vehicles because cracks in the microprocessor may stop the rearview camera image displaying properly.

    Product
    DODGE — DODGE, RAM JOURNEY, PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E051000·2025-08-25

    Truck Certification Services Recalls Load Carrying Capacity Labels

    Truck Certification Services is recalling specific Load Carrying Capacity labels where weight units may be reversed, potentially leading to vehicle overloading.

    Product
    EQUIPMENT:OTHER:LABELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V541000·2025-08-22

    Ford Recalls 2024-2026 Rangers Due to Side Air Bag Defect

    Ford is recalling 2024-2026 Ranger vehicles because side curtain air bags may tear during deployment, increasing injury risk.

    Product
    FORD — FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V538000·2025-08-22

    2026 Forest River Flagstaff and Rockwood trailers recalled for inoperative breakaway switch

    Forest River is recalling certain 2026 Flagstaff and Rockwood recreational trailers because the breakaway switch was wired to the incorrect side of the battery disconnect switch, making it inoperative. An inoperative breakaway switch increases the risk of a crash.

    Product
    FOREST RIVER — FOREST RIVER FLAGSTAFF, ROCKWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V543000·2025-08-22

    Ford Explorer and Aviator may not illuminate trailer tail lights

    Ford is recalling certain 2025 Explorer and Lincoln Aviator vehicles because an improperly manufactured body control module may leave a towed trailer's tail lights unlit. This fails FMVSS 108.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V546000·2025-08-22

    Ford Mustang water ingress can disable tail and marker lights

    Ford is recalling certain 2024-2025 Mustang and Mustang GTD vehicles because water may enter the body control module and cut communication with the licence plate, side marker and tail lights.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V540000·2025-08-22

    Ford 2025–2026 F-series trucks instrument panel cluster failure recall

    Ford is recalling certain 2025–2026 F-150, F-250 SD, F-350 SD, F-450 SD, and F-550 SD vehicles because the instrument panel cluster may fail at startup, preventing display of critical information like warning lights and vehicle speed.

    Product
    FORD — FORD F-150, F-250 SD, F-350 SD, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide