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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11676–11700 of 114063

  • HighUSDA FSIS·PHA-01082025-01·2025-01-08

    Chicken Curry Empanadas Recalled For Undeclared Milk Allergen

    USDA FSIS issued a public health alert for Chicken Curry Empanadas that may contain undeclared milk. Consumers with milk allergies should not consume these products.

    Product
    Rajbhog Foods (NJ), Inc. — FSIS Issues Public Health Alert For Chicken Empanada Products Due To Misbranding And Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0791-2025·2025-01-08

    Medline Deep Brain Stimulation Surgical Kits Recalled for Non-Sterile Contamination

    Medline has recalled 128 Deep Brain Stimulation surgical kits for containing non-sterile Surgical Patties and Strips with potential endotoxin contamination. Affected units were distributed worldwide including the US, UAE, and Canada.

    Product
    Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION PACK-LF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0772-2025·2025-01-08

    SynchroMed II and III implantable pumps recalled for software issues

    Medtronic recalled SynchroMed II and III implantable pumps for software issues in the clinician tablet application. Fifty-nine systems are affected.

    Product
    SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CLINICIAN TABLET UK with the A810 CP app version 2.x, CFN CT900C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0173-2025·2025-01-08

    Ketamine injection syringes recalled due to missing tamper-evident seals

    Hikma Injectables is recalling 1,800 ketamine injection syringes nationwide because tamper-evident seals are not attached to several syringes, compromising sterility assurance.

    Product
    ketamine inj 50 mg per 1 mL, Rx Only, 1 mL fill in a 3mL pre-filled syringe, For IV or IM Use, Hikma Injectables USA Inc., 36 Stults Road, Dayton, NJ 08810, This is a Compounded Drug. Hospital/Office Use Only. NDC 63037-137-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0323-2025·2025-01-08

    Multiple watermelon brands recalled due to Listeria contamination risk

    Gracie's Kitchens Inc. is recalling watermelon products from multiple brands due to potential Listeria monocytogenes contamination. Affected products were sold in Connecticut and New York with sell-by dates from November 9-21, 2024.

    Product
    a.) King Kullen brand Watermelon Slices; UPC 85316-10006; 20 oz foam tray b) Wild By Nature brand Watermelon Slices; UPC: 85316-10006; 20 oz foam tray c.) King Kullen brand Watermelon Chunks; UPC: 85316-10413; 12 oz plastic container d.) King Kullen brand Watermelon Slices; UPC:
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0353-2025·2025-01-08

    Gracie's Kitchen Cauliflower Florets Recalled Due to Listeria Risk

    Gracie's Kitchens Inc. is recalling Gracie's Kitchen brand Cauliflower Florets due to potential Listeria monocytogenes contamination. Affected product has sell-by dates from November 14-24, 2024, and was distributed in Connecticut and New York.

    Product
    a.) Gracie's Kitchen brand Cauliflower Florets; UPC: 85316-10012; 12 oz foam tray
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0346-2025·2025-01-08

    Fruit Platters Recalled Due to Potential Listeria Contamination

    Fruit Platters sold under King Kullen and Gracie's Kitchen brands may contain Listeria monocytogenes. Consumers in Connecticut and New York who purchased products with November 11-21, 2024 sell-by dates should not eat them.

    Product
    a.) King Kullen brand Large Fruit Platter; UPC: 85316-10402; 56 oz plastic container b.) Gracie's Kitchen brand Large Fruit Platter; UPC: 85316-10402; 56 oz plastic container
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0787-2025·2025-01-08

    Medline Surgical Procedure Kits Recalled Due to Sterility Concerns

    Medline is recalling custom surgical procedure kits that contain non-sterile surgical supplies with potential for endotoxin contamination. The kits were distributed worldwide, including the United States, United Arab Emirates, and Canada.

    Product
    Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF, REF DYNJ39461J; 2) NEURO BASIN KIT, REF DYNJ80200B.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0167-2025·2025-01-08

    Levothyroxine Sodium tablets recalled for impurity specification failure

    Lupin Pharmaceuticals is recalling Levothyroxine Sodium 75 mcg tablets due to out-of-specification impurities detected in stability testing. Affected lot LA01276 (expiring 07/2026) was distributed to one Ohio distributor.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Food)·F-0329-2025·2025-01-08

    Diced White Onions Recalled for Potential Listeria Contamination

    Gracie's Kitchens Inc. is recalling diced white onion products due to potential Listeria monocytogenes contamination. Multiple brands (King Kullen, Wild By Nature, Gracie's Kitchen) are affected; products were distributed in Connecticut and New York.

    Product
    a.) King Kullen brand Diced White Onion; UPC: 85316-10083; 12 oz plastic container b.) Wild By Nature brand Diced White Onion; UPC: 85316-10085; 12 oz plastic container c.) Gracie's Kitchen brand Diced White Onion; UPC: 85316-10018; 10 oz plastic container d.) Gracie's Kitchen br
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0796-2025·2025-01-08

    Rigid Intracardiac Sucker Units Recalled for Potential Sterility Breach

    Med Michigan Holding recalls SUC-4300S Rigid Intracardiac Suckers due to incomplete or partial pouch seals that may compromise sterility during cardiac surgery.

    Product
    SUC-4300S, Rigid Intracardiac Sucker Fluted Tip; 1/4" (6.4mm) connector 13" (33cm) length. Indicated for handheld use only to remove excess fluid from the surgical field.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0771-2025·2025-01-08

    Medtronic SynchroMed II and III Implantable Pumps Recalled for Software Defects

    Medtronic is recalling SynchroMed II and III implantable pumps used with a clinician tablet app that has software issues in version 2.x. Approximately 319 systems were distributed worldwide.

    Product
    SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK with the A810 CP app version 2.x, CFN CT900B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0782-2025·2025-01-08

    Medical Device Kits Recalled for Non-Sterile Surgical Components

    Medline Industries is recalling See DocMan custom convenience kits that contain non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. Approximately 48,655 units were distributed worldwide.

    Product
    See DocMan
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0175-2025·2025-01-08

    Carboxymethylcellulose sodium eye drops recalled for label mix-up

    AvKARE is recalling Carboxymethylcellulose Sodium Ophthalmic Solution eye drops due to a label mix-up. The recall affects 16,677 cartons distributed nationwide.

    Product
    CARBOXYMETHYLCELLULOSE SODIUM — CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0375-2025·2025-01-08

    Wegmans Jalapeno Baked Cheese Puffs Recalled for Undeclared MSG

    Herr Foods Inc is recalling Wegmans Jalapeno Baked Cheese Puffs due to undeclared monosodium glutamate and flavor compounds. Affected units have expiration dates from December 2024 through May 2025.

    Product
    Wegmans Jalapeno Baked Cheese Puffs, Jalapeno flavored, 10oz, (283 g), SKU #6877
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0168-2025·2025-01-08

    AvKARE Nitrofurantoin 100 mg Capsules Recalled for Dissolution Failures

    AvKARE is recalling Nitrofurantoin 100 mg capsules (NDC 50268-625-15, lot 47101, exp. 02/2026) nationwide because they failed dissolution specifications. Affected users should consult their healthcare provider.

    Product
    Nitrofurantoin Capsules, USP, 100 mg, 50 Capsules (5 x 10) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478. NDC#: 50268-625-15.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0176-2025·2025-01-08

    Eye drops recalled nationwide due to labeling mix-up

    AvKARE is recalling Polyvinyl Alcohol Ophthalmic Solution eye drops due to a labeling mix-up. The recall affects Lot #0160 and was distributed nationwide.

    Product
    POLYVINYL ALCOHOL — POLYVINYL ALCOHOL (POLYVINYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0770-2025·2025-01-08

    Auryon Laser Atherectomy System Recalled for Activation Failure

    Angiodynamics is recalling 138 units of the Auryon atherectomy laser system due to potential failure to advance to activation mode during use. This malfunction could cause procedural delays or interruptions.

    Product
    AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number: EXM-2001-1100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0171-2025·2025-01-08

    Dapsone Gel Recalled Nationwide for Crystallization

    Viona Pharmaceuticals is recalling Dapsone Gel 7.5% nationwide due to crystallization detected in multiple lots. Patients should contact their pharmacy or healthcare provider for guidance.

    Product
    DAPSONE — DAPSONE (DAPSONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·25V002000·2025-01-06

    Tesla Model X, Model Y, Model S, and Model 3 Rearview Camera Loss

    Tesla is recalling certain 2023–2025 Model X, Model Y, Model S, and Model 3 vehicles because the computer circuit board may short, disabling the rearview camera image. This reduces rear visibility and increases crash risk.

    Product
    TESLA — TESLA MODEL 3, MODEL S, MODEL Y, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-01052025-01·2025-01-05

    Frozen Raw Ground Beef Recalled for Foreign Matter Contamination

    USDA FSIS issued a public health alert for frozen raw ground beef from Stockyards Packing Co. due to possible hard plastic and metal contamination.

    Product
    Stockyards Packing Co LLC — FSIS Issues Public Health Alert for Frozen, Raw Ground Beef Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • HighCPSC·25081·2025-01-02

    Euqee Wintergreen Essential Oil Recalled for Unsafe Packaging

    Euqee Wintergreen Essential Oils sold on Amazon.com are recalled because their packaging is not child-resistant, violating federal law. Methyl salicylate in the oil could poison young children if swallowed.

    Product
    Euqee Wintergreen Essential Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V001000·2025-01-02

    Aston Martin Vehicles Recalled: Infotainment Display Obstructs Rearview Camera

    Aston Martin is recalling certain 2024-2025 DB12, Vantage, and DBX707 vehicles. The infotainment home screen menu may obstruct the rearview camera when in reverse, reducing rear visibility and increasing the risk of a crash.

    Product
    ASTON MARTIN — ASTON MARTIN DB12, DBX707, VANTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25083·2025-01-02

    John Deere ZTrak Zero-Turn Mowers Recalled for Fire and Burn Hazards

    Kawasaki is recalling about 39,000 John Deere ZTrak zero-turn mowers with Kawasaki engines because the voltage regulator can fail, causing the engine to overheat and creating fire and burn hazards. No injuries have been reported to date.

    Product
    John Deere ZTrak™ Zero Turn Mowers with Kawasaki Engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide