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 the agency’s own highest classification or reported deaths or serious injuries, 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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51–75 of 39702

  • SevereFDA (Food)·H-0002-2027·2026-10-14

    LEASA Living Alfalfa Sprouts Recalled for Potential E. coli Contamination

    LEASA Living Alfalfa Sprouts are being recalled because the seeds may have been contaminated with E. coli. The product was distributed in Florida and New Hampshire.

    Product
    LEASA Living Alfalfa Sprouts; packaged in plastic clamshell containers; KEEP REFRIGERATED; NET WT. 4 OZ. (113g); Grown & Packaged by: LEASA Industries Co., Inc., Mami FL 33147; Product of USA; UPC: 0 75465 55912 7
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0009-2027·2026-10-14

    K.C. Pharmaceuticals Recalls Leader Ultra Lubricating Eye Drops for Sterility Concerns

    K.C. Pharmaceuticals is recalling 163,008 cartons of Leader Ultra Lubricating Eye Drops due to a lack of assurance of sterility. The product was distributed nationwide under multiple brand names.

    Product
    LEADER ULTRA LUBRICATING EYE DROPS — LEADER ULTRA LUBRICATING EYE DROPS (POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0024-2027·2026-10-14

    FDA Recalls Tri-MIX Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Tri-MIX injectable syringes because processing equipment used may have compromised the product's sterility.

    Product
    Tri-MIX (PAPAV/PHENTO/ALPROS), 30/1/40, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0026-2027·2026-10-14

    Carolina Infusion Recalls Semaglutide/Cyanocobalamin Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling semaglutide/cyanocobalamin injectable products due to a lack of assurance of sterility related to formulation and processing equipment.

    Product
    SEMAGLUTIDE/CYANOCOBALAMIN 9/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0030-2027·2026-10-14

    FDA Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 85/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.

    Product
    TIRZEPATIDE/CYANOCOBALAMIN 85/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936;
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0006-2027·2026-10-14

    K.C. Pharmaceuticals Recalls Dry Eye Relief Eye Drops for Sterility Concerns

    K.C. Pharmaceuticals is recalling 1,327,248 cartons of dry eye relief eye drops due to a lack of assurance of sterility. The products were distributed nationwide under multiple brand names.

    Product
    LEADER DRY EYE RELIEF EYE DROPS — LEADER DRY EYE RELIEF EYE DROPS (GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0071-2027·2026-10-14

    Steris VERIFY Biological/Integrator Challenge Pack Recall for Spore Population Defect

    Steris is recalling VERIFY Biological/Integrator Challenge Packs because the spore population may be too low, potentially causing false results in steam sterilization monitoring.

    Product
    VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0036-2027·2026-10-14

    Apothecary Pharma Recalls Tirzepatide Injection Vials Due to Sterility Concerns

    Apothecary Pharma LLC is recalling 22 vials of Tirzepatide Injection due to a lack of assurance of sterility. The affected product was distributed nationwide.

    Product
    Tirzepatide Injection, 18mg/mL, 4 mL Sterile Multi-Dose Vial, Rx only, Apothecary Pharma, LLC, 1913 Evans Road, Cary, NC 27513, NDC 85091-001-18.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0003-2027·2026-10-14

    Good Sense Eye Drops Recalled for Lack of Sterility Assurance

    K.C. Pharmaceuticals is recalling Good Sense Eye Drops Irritation Relief and related brands due to a lack of assurance of sterility.

    Product
    GOODSENSE EYE DROPS IRRITATION RELIEF — GOODSENSE EYE DROPS IRRITATION RELIEF (TETRAHYDROZOLINE HCL, ZINC SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0008-2027·2026-10-14

    K.C. Pharmaceuticals Recalls Multiple Brands of Eye Drops for Sterility Concerns

    K.C. Pharmaceuticals is recalling multiple brands of eye drops, including Leader, Equate, and Walgreens, due to a lack of assurance of sterility.

    Product
    LEADER EYE DROPS REDNESS RELIEF — LEADER EYE DROPS REDNESS RELIEF (GLYCERIN, NAPHAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0086-2027·2026-10-14

    Medline Bariatric Rollator Recalled Due to Front Wheel Detachment Risk

    Medline is recalling 1,824 bariatric rollators because the front wheel assembly may detach, posing a risk of falls and serious injury.

    Product
    Rollator, Bariatric, Basic Steel, Burgundy, mechanical walker with four legs and a metal frame intended for medical purposes to provide moderate weight support while walking, Product Number MDS86800XWS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E071000·2026-10-14

    KTM Recalls Steering Dampers for Super Duke Motorcycles

    KTM is recalling certain Müller Präzision steering dampers for 2020-2026 KTM Super Duke R and Evo motorcycles because they can loosen, leading to loss of steering control.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0088-2027·2026-10-14

    Medtronic MiniMed Flex Insulin Pumps Recalled for Failed Verification Tests

    Medtronic is recalling 20 MiniMed Flex insulin pumps that failed or lacked verification test results, posing risks of inaccurate insulin delivery and device malfunctions.

    Product
    Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog Numbers: MMT-8062; MMT-8072 Product Description: The MiniMed Flex pump is an alternate controller enabled (ACE) pump intended for the subcutaneous delivery of insulin, at set and variable rates, for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0022-2027·2026-10-14

    FDA Recalls Tri-MIX Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to processing equipment.

    Product
    Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/20, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0016-2027·2026-10-14

    FDA Recalls X10 Supplement Containing Undeclared Sildenafil and Tadalafil

    A&P CREATIONS is recalling X10 Natural Enhancement Supplement because it contains undeclared Sildenafil and Tadalafil.

    Product
    X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC: 7708075247094, Manufactured by FutuPro S.A.S., Colombian Industry; Distributed by Natur Fuel, 2725 Armstrong Avenue, Clermont, FL 34714.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0002-2027·2026-10-14

    K.C. Pharmaceuticals Recalls Artificial Tears Due to Sterility Concerns

    K.C. Pharmaceuticals is recalling 505,896 cartons of artificial tears sold under multiple brands because the product lacks assurance of sterility.

    Product
    LEADER ARTIFICIAL TEARS 15 ML — LEADER ARTIFICIAL TEARS 15 ML (POLYVINYL ALCOHOL, POVIDONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0003-2027·2026-10-14

    LEASA Alfalfa Sprouts Recalled Due to Possible E. coli Contamination

    LEASA Industries is recalling 1,416 cups of alfalfa sprouts because the seeds may have been contaminated with E. coli.

    Product
    LEASA Alfalfa Sprouts; packaged in plastic clamshell containers; KEEP REFRIGERATED; NET WT. 6 OZ. (170g); Grown & Packaged by: LEASA Industries Co., Inc., Mami FL 33147; Product of USA; UPC: 0 75465 11111 0
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0020-2027·2026-10-14

    Carolina Infusion Recalls Sermorelin Acetate Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Sermorelin Acetate 1 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.

    Product
    SERMORELIN ACETATE 1 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0028-2027·2026-10-14

    Carolina Infusion Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling specific lots of Tirzepatide/Cyanocobalamin 64/2 mg/mL injectable because the product may lack assurance of sterility.

    Product
    TIRZEPATIDE/CYANOCOBALAMIN 64/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0018-2027·2026-10-14

    Carolina Infusion Recalls Semaglutide Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Semaglutide 3 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.

    Product
    SEMAGLUTIDE 3 MG/ML INJECTABLE, 8 x 0.1 mL syringes, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0019-2027·2026-10-14

    FDA Recalls Semaglutide/Cyanocobalamin Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling semaglutide/cyanocobalamin injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.

    Product
    SEMAGLUTIDE/CYANOCOBALAMIN 3/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0017-2027·2026-10-14

    FDA Recalls Tirzepatide Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Tirzepatide 26 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.

    Product
    TIRZEPATIDE 26 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936;
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0074-2027·2026-10-14

    Steris Recalls VERIFY Biological Steam Test Packs Due to Spore Population Concerns

    Steris Corporation is recalling 217 VERIFY Biological Steam Test Packs because the spore population may fall below specifications, potentially causing false sterilization results.

    Product
    VERIFY Biological Steam Test Pack Model/Catalog Number: S3065
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0025-2027·2026-10-14

    FDA Recalls Tri-MIX Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Tri-MIX injectable syringes because processing equipment used in compounding raised concerns about the product's sterility.

    Product
    Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/60, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0007-2027·2026-10-14

    K.C. Pharmaceuticals Recalls Good Sense Eye Drops for Sterility Concerns

    K.C. Pharmaceuticals is recalling Good Sense Eye Drops Original Formula due to a lack of assurance of sterility. The recall affects 1,025,448 cartons distributed nationwide.

    Product
    GOODSENSE EYE DROPS ORIGINAL FORMULA — GOODSENSE EYE DROPS ORIGINAL FORMULA (TETRAHYDROZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide