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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7051–7075 of 7514

  • SevereFDA (Food)·F-0074-2022·2021-11-03

    Nature's Heart Mango Turmeric Cashew Mix Recalled for Undeclared Peanuts

    Nestle USA Inc. is recalling Nature's Heart Mango Turmeric Cashew Glazed Mix 1.5oz pouches due to undeclared peanut allergen. The product was distributed across 32 states.

    Product
    Nature's Heart Mango Turmeric Cashew Glazed Mix 1.5oz poly film pouches - 32 units per case
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Drugs)·D-0044-2022·2021-11-03

    TEST CYP 200MG/ML injection recalled due to sterility assurance concerns

    Red Mountain Compounding Pharmacy is recalling TEST CYP 200MG/ML MDV ETHYL OLEATE due to FDA inspection findings of lack of assurance of sterility. The product was distributed to approximately 494 patients across seven states.

    Product
    TEST CYP 200MG/ML MDV ETHYL OLEATE, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0038-2022·2021-11-03

    Glutathione 200mg/mL MDV Recalled Due to Sterility Assurance Concerns

    Red Mountain Compounding Pharmacy is recalling Glutathione 200mg/mL MDV (multiple-dose vials) because FDA inspection identified concerns that the product may lack proper sterility assurance. The product was distributed to patients in multiple states.

    Product
    GLUTATHIONE 200MG/ML MDV, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0048-2022·2021-11-03

    Compounded Anabolic Steroid Product Recalled for Sterility Assurance Concerns

    Red Mountain Compounding Pharmacy is recalling a compounded anabolic steroid product due to FDA concerns about sterility assurance identified during inspection. The product was distributed to approximately 494 patients in seven states.

    Product
    TEST CYP/PROP/DECA-NAN 125MG/ML (80/10/10) IN SESAME OIL, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Food)·F-0072-2022·2021-11-03

    Nature's Heart Toasted Coconut Chips recalled for undeclared peanuts

    Nestle USA is recalling Nature's Heart Toasted Coconut Chips 1.5oz pouches because they contain undeclared peanuts, posing a serious risk to consumers with peanut allergies.

    Product
    Nature's Heart Toasted Coconut Chips 1.5oz poly film pouches - 32 units per case
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Drugs)·D-0058-2022·2021-11-03

    Methylcobalamin Injectable Recalled Due to Sterility Assurance Concerns

    Red Mountain Compounding Pharmacy is recalling methylcobalamin 10,000 MCG/ML multi-dose vials after FDA inspection identified sterility assurance concerns.

    Product
    METHYLCOBALAMIN 10,000MCG/ML MDV INJ, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0037-2022·2021-11-03

    Estradiol Valerate Injection Recalled for Sterility Assurance Concerns

    Red Mountain Compounding Pharmacy is recalling Estradiol Valerate 5mg/mL injectable medication due to FDA inspection findings of inadequate sterility assurance. The product was distributed to approximately 494 patients across seven states.

    Product
    ESTRADIOL VALERATE 5MG/ML MDV INJ, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0066-2022·2021-11-03

    Progesterone 100mg/ml Oil Injection Recall: Sterility Assurance Defect

    Red Mountain Compounding Pharmacy is recalling Progesterone 100mg/ml MDV Oil Injection due to lack of assurance of sterility following FDA inspection. About 494 patients in seven states received prescriptions for this affected product.

    Product
    PROGESTERONE 100MG/ML MDV OIL INJECTION, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereNHTSA·21V849000·2021-11-01

    Heartland Cyclone and Road Warrior RVs recalled for loose electrical wires

    Heartland Recreational Vehicles is recalling 2019-2021 Road Warrior and 2020-2021 Cyclone trailers because wire securement lugs may be improperly tightened. Loose wires can cause electrical arcing and increase fire risk.

    Product
    HEARTLAND — 2020 HEARTLAND ROAD WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0010-2022·2021-10-27

    Coppertone Pure & Simple 50 Sunscreen Spray Recalled for Benzene Contamination

    Beiersdorf Inc. is recalling Coppertone Pure & Simple 50 Sunscreen Spray due to the presence of benzene, a chemical contaminant. The recall affects 38,328 cans distributed nationwide.

    Product
    Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02880 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0022-2022·2021-10-27

    Kalona Supernatural Organic Whole Chocolate Milk Recall for Improper Pasteurization

    Kalona Supernatural Organic Whole Chocolate Milk was distributed without proper pasteurization. The product was sold in 16 FL OZ, 32 FL OZ, and 64 FL OZ bottles across seven states.

    Product
    Kalona Supernatural Organic Whole Chocolate Milk, Manufactured in Iowa for Kalona Organics, LLC. Kalona IA in 16 FL OZ (UPC 8-81245-10516-9, 8 bottles per case) 32 FL OZ (UPC 8-81245-10532-9, 6 bottles per case) and 64 FL OZ (UPC8-81245-10564-0, 6 bottles per case)
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0011-2022·2021-10-27

    Coppertone Pure & Simple Kids 50 Sunscreen Spray Recalled for Benzene Contamination

    Beiersdorf Inc. is recalling Coppertone Pure & Simple kids 50 Sunscreen Spray due to the presence of benzene, a chemical contaminant. The affected product was distributed nationwide.

    Product
    Coppertone Pure & Simple kids 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02882 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0064-2022·2021-10-27

    Lightly Salted Cashew Halves & Pieces recalled for glass contamination

    Suntree Snack Foods is recalling Lightly Salted Cashew Halves & Pieces (16 oz., UPC 842379195341) due to the presence of glass pieces in the product. The recall affects approximately 4,200 bags distributed across 11 states and Washington, D.C.

    Product
    Lightly Salted Cashew Halves & Pieces, 16 oz., UPC 842379195341. 6 bags/case.
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0107-2022·2021-10-27

    Infusion Pump Air Detector Malfunction May Prevent Alarm to Clinician

    Smiths Medical CADD-Solis VIP ambulatory infusion pumps may fail to detect air in the infusion line and alert clinicians due to intermittent air-detector malfunction.

    Product
    CADD-Solis VIP ambulatory infusion pump, Model Numbers: a. 21-2120-0105-02L b. 21-2120-0105-03L c. 21-2120-0105-06L d. 21-2120-0105-07L e. 21-2120-0105-08L f. 21-2120-0105-12L g. 21-2120-0105-13L h. 21-2120-0105-14L i. 21-2120-0105-15L j. 21-2120-0105-17L k. 21-2120-01
    Category
    Medical Device
    Distribution
    1 state
  • SevereCPSC·22009·2021-10-27

    myCharge Powerbanks Recalled Due to Fire and Burn Hazards

    myCharge is recalling approximately 67,000 powerbanks sold from August 2018 through December 2019 because the lithium-ion battery can overheat and ignite, posing fire and burn hazards. The company has received 30 overheating reports resulting in seven injuries and property damage.

    Product
    myCharge powerbanks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0055-2022·2021-10-27

    Roasted Salted Cashew Halves and Pieces recalled for glass contamination

    Suntree Snack Foods is recalling Roasted Salted Cashew Halves and Pieces due to the presence of glass pieces in the product. The recall affects 960 cases distributed across multiple states.

    Product
    Roasted Salted Cashew Halves and Pieces, 8 oz. , UPC 072036734891. 8 bags/case.
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Drugs)·D-0023-2022·2021-10-27

    AirDuo Digihaler 55/14 Inhalation Powder Recalled for Subpotent Dose

    Teva Pharmaceuticals is recalling AirDuo Digihaler 55/14 inhalation powder due to subpotent emitted dose of salmeterol. Approximately 1,978 inhalers distributed nationwide may deliver less medication than labeled.

    Product
    AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva Respiratory, LLC Frazer, PA 19355, Manufactured in Ireland, NDC 59310-111-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0013-2022·2021-10-27

    Coppertone SPORT MINERAL 50 Sunscreen Spray Recalled for Benzene Contamination

    Beiersdorf Inc. is recalling Coppertone SPORT MINERAL 50 Sunscreen Spray due to the presence of benzene, a chemical contaminant. The recall affects 142,236 cans distributed nationwide.

    Product
    Coppertone SPORT MINERAL 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02870 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0063-2022·2021-10-27

    Mountain Trail Mix Recalled for Potential Glass Contamination

    Suntree Snack Foods is recalling Mountain Trail Mix (28 oz., UPC 814314024146, Lot 86960) because a customer reported finding glass pieces in the product. The affected cases were distributed to multiple states.

    Product
    Mountain Trail Mix, 28 oz. , UPC 814314024146. 6 bags/case.
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-0023-2022·2021-10-27

    SunGarden Mung Bean Sprouts Recall for Listeria monocytogenes

    SunGarden Mung Bean Sprouts (5lb and 10lb packages) are being recalled because the product tested positive for Listeria monocytogenes. The affected lots were distributed to a customer in Florida.

    Product
    SunGarden Mung Bean Sprouts 5lb & 10lb packaged in clear plastic bag in white cardboard box
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0020-2022·2021-10-27

    Kalona Supernatural Organic Whipping Cream Recalled for Improper Pasteurization

    Kalona Supernatural Organic Whipping Cream was shipped without proper pasteurization, creating a potential food safety risk. The recall affects 16 FL OZ and 32 FL OZ bottles distributed to retailers in multiple states.

    Product
    Kalona Supernatural Organic Whipping Cream, Manufactured in Iowa for Kalona Organics, LLC. Kalona IA in 16 FL OZ (UPC 8-81245-12016-2, 8 bottles per case) and 32 FL OZ (UPC 8-81245-12032-2, 6 bottles per case)
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0012-2022·2021-10-27

    Coppertone Pure & Simple Baby Sunscreen Spray Recalled for Benzene Contamination

    Beiersdorf Inc. is recalling Coppertone Pure & Simple Baby 50 Sunscreen Spray nationwide due to the presence of benzene, a chemical contaminant. Consumers should stop using affected products immediately.

    Product
    Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02881 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0091-2022·2021-10-27

    Cardiosave Li-Ion battery pack recalled for insufficient runtime specification

    Datascope Corp. is recalling Cardiosave Li-Ion battery packs that failed to meet minimum runtime requirements. These nonconforming batteries were inadvertently released to customers worldwide.

    Product
    Cardiosave Li-Ion Battery Pack, Part No. 0146-00-0097. Component of the Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) with the below Model Numbers. 1. Cardiosave Hybrid. Model Numbers: 0998-00-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-00-0800-35, 0998-00-0800-36, 099
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0014-2022·2021-10-27

    Coppertone SPORT Sunscreen Spray recalled for benzene contamination

    Beiersdorf Inc. is recalling Coppertone SPORT Sunscreen Spray 50 (1.6 oz cans) nationwide due to the presence of benzene, a known carcinogen. Affected lot TN00BU3 expires 05/31/2024.

    Product
    Coppertone SPORT Sunscreen Spray 50, (To Deliver) Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 5%, NET WT 1.6 OZ (45 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 41100 00506 9
    Category
    Drug
    Distribution
    Distributed nationwide