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.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

10976–11000 of 31361

SevereFDA (Food)·F-1837-2024·2024-10-09
Chicken and Duck Eggs Recalled for Potential Salmonella Contamination
Milo's Poultry Farms is recalling chicken and duck eggs sold in foodservice and consumer packages in Illinois, Michigan, and Wisconsin due to potential Salmonella contamination.
Product
Grade A Brown Chicken Eggs, in shell, Bulk 15 dozen. For Foodservice. Keep Refrigerated. Sold with the following brands: 1. Milo's Poultry Farms, N 3873 Valley Road, Bonduel, WI 54107. Organic Eggs from Free Range Hens. 2. M&E Family Farms, Eggs from Free Range Hens. N
Category
Food
Distribution
3 states
SevereFDA (Food)·F-0016-2025·2024-10-09
Raisin Bran Muffins Recalled for Undeclared Milk and Wheat Allergens
The Posh Bakery, Inc. is recalling Whole Grains Bakery Raisin Bran Muffins (6 oz) due to undeclared whey (milk) and wheat allergens and missing allergen labeling.
Product
Whole Grains Bakery labeled "Raisin Bran Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC "7 13583 05 104 7"
Category
Food
Distribution
0 states
SevereFDA (Drugs)·D-0003-2025·2024-10-09
Hard Steel Capsules Recalled for Undeclared Acetaminophen and Sildenafil
Hard Steel Capsules contain undeclared acetaminophen and sildenafil and were marketed without FDA approval. All 729 units distributed nationwide and internationally are included in the recall.
Product
Hard Steel Capsules packaged in 1 count blister packs in boxes of 10, 20 and 30, Manufactured in U.S.A.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0001-2025·2024-10-09
MiniMed Insulin Pumps Recalled for Battery Depletion and Delivery Risk
Medtronic MiniMed 630G and 700G insulin pumps may experience battery depletion and device shutdown after physical impact, interrupting insulin delivery in diabetic patients.
Product
MiniMed 630G Insulin Pump, REF: MMT-1515, MMT-1714, MMT-1715, MMT-1754, MMT-1755; MiniMed 700G Insulin Pump, REF: MMT-1800, MMT-1801, MMT-1805, MMT-1850, MMT-1851
Category
Medical Device
Distribution
53 states
HighFDA (Food)·F-0022-2025·2024-10-09
Cranberry Muffins Recalled for Undeclared Milk and Wheat Allergens
The Posh Bakery is recalling Cranberry Muffins due to undeclared whey (milk) and wheat flour, as well as missing nutrition facts panel and allergen statement. Consumers with milk or wheat allergies should not consume these products.
Product
Whole Grains Bakery labeled "Cranberry Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-3303-2024·2024-10-09
Urinalysis reagent strips recalled for reduced protein detection sensitivity
Healgen Scientific is recalling 1,636,994 urinalysis test strips in California, Georgia, and Texas due to reduced protein detection sensitivity that may produce false negative results and delay kidney disease diagnosis.
Product
Healgen Series Reagent strips for Urinalysis are composed of several color pads aligned on a test strip. Each pad is employed for testing one assay item by visually or instrumentally reading the color change of the pad and comparing with the corresponding blocks on a color chart.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0002-2025·2024-10-09
Kerala Mixture Snack Recalled for Undeclared Wheat Allergen
Grace Imports recalled Kerala Mixture snack due to undeclared wheat allergen. The supplier failed to disclose wheat on the product label, posing a risk to consumers with wheat allergies.
Product
KERALA MIXTURE INGREDIENTS: Gram Flour 48%, Edible Veg Oil (Refined Palmolein Oil) 36%, Peanuts 6%, Roasted Bengal Gram, Salt 1.5%, Chilly powder 1%, Curry leaf, Asafoetida, Natural Antioxidant (Mixed Tocopherol INS 305) ALLERGEN INFORMATION: Made in a Factory that Process Peanut
Category
Food
Distribution
0 states
HighNHTSA·24V668000·2024-10-09
Freightliner and Western Star brake lights may fail during emergency braking
Daimler Trucks is recalling certain Freightliner and Western Star trucks because brake lights may fail to illuminate during automatic emergency braking, increasing crash risk. Dealers will update software at no cost.
Product
FREIGHTLINER — 2025 FREIGHTLINER EM2
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0007-2025·2024-10-09
Pluvicto Radiopharmaceutical Drug Recalled Due to Manufacturing Quality Deviations
Advanced Accelerator Applications is recalling 99 doses of Pluvicto (lutetium LU-177 injection) due to manufacturing quality deviations. The affected lots were distributed to six states.
Product
Pluvicto, 1000 MBq/mL (27 mCi/mL), lutetium, LU 177, vipivotide tetraxetan injection, Single-dose vial, Sterile, Manufacturer Advanced Accelerator Applications, 57 E. Willow Street, NJ 07041, Millburn USA. NDC 69488-0010-61
Category
Drug
Distribution
6 states
HighFDA (Devices)·Z-3310-2024·2024-10-09
BIOFINITY XR TORIC Contact Lenses Recalled for Misaligned Axis Defect
CooperVision is recalling 607 BIOFINITY XR TORIC soft contact lenses due to a manufacturing defect with misaligned axis, resulting in incorrect power and poor visual acuity. The lenses were distributed in the US and Canada.
Product
BIOFINITY XR TORIC Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia with astigmatism) with presbyopia in aphakic and non-aphakic persons.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3309-2024·2024-10-09
Stryker Tornier Shoulder Implant Insert May Not Seat Securely
Tornier Inc. is recalling 38 Stryker Tornier Perform Humeral System Reversed Inserts (model REF DWP2393) due to inverted locking rings. The defect may prevent the insert from seating securely in the implant stem or spacer.
Product
Stryker Tornier Perform Humeral System, Reversed Insert, 45%, REF DWP2393, for shoulder arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V650000·2024-10-09
2024 Hyundai Kona Seat Belt Retractor Malfunction Recall
Hyundai is recalling certain 2024 Kona vehicles because the rear seat belt retractors may not function properly. A defective seat belt could fail to restrain occupants in a crash, increasing injury risk.
Product
HYUNDAI — 2024 HYUNDAI KONA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3305-2024·2024-10-09
Atellica IM aTPO Assay Diagnostic Test Recalled for Measurement Bias
Siemens Healthcare Diagnostics is recalling 9783 kits of the Atellica IM aTPO Assay diagnostic test due to positive bias in patient results below the 60 U/mL cut-off level, which may produce inaccurate test results.
Product
Atellica IM aTPO Assay, Material Number 10995466 (100 Test) and 10995467 (500 Test)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1836-2024·2024-10-09
Mini Raspberry Lemon Coffee Cake Recalled for Undeclared Walnuts and Wheat
Mini Raspberry Lemon Coffee Cake products in Washington were mislabeled and contain undeclared walnuts and wheat. Consumers with allergies to these ingredients should not consume the product and should return it to the store.
Product
Mini Raspberry Lemon Coffee Cake, net wt. 13.5oz. UPC 8 57297 00745 4. Made with Gluten-Free Ingredients in a Gluten-Friendly Bakery. Macrina Bakery - Kent, WA. Ingredients: CANE SUGAR, GREEK YOGURT (GRADE A PASTEURIZED CULTURED MILK, CREAM, NONFAT MILK), EGGS, RASPBERRIES, B
Category
Food
Distribution
1 state
HighFDA (Food)·F-0017-2025·2024-10-09
Chocolate chip muffins recalled for undeclared milk and wheat
The Posh Bakery is recalling Whole Grains chocolate chip muffins due to undeclared milk and wheat allergens with missing allergen labeling. Those with milk or wheat allergies should not consume this product.
Product
Whole Grains Bakery labeled "Choclate Chip Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC"7 13583 05 105 4"
Category
Food
Distribution
0 states
HighFDA (Food)·F-0014-2025·2024-10-09
Poppy Seed Muffins Recalled Due to Undeclared Milk, Wheat, and Almond Allergens
The Posh Bakery is recalling 6-ounce Poppy Seed Muffins due to undeclared milk (whey), wheat, and almond allergens. The product lacks required allergen labeling, posing a risk to consumers with allergies.
Product
Whole Grains Bakery labeled "Poppy Seed Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC "7 13583 05 103 0"
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-0008-2025·2024-10-09
Dental Ultrasonic Cleaner Recalled for Bacterial Contamination
Young Dental Manufacturing is recalling BIOTROL PURIT Clean-It Ultrasonic Cleaner (REF PC016) due to bacterial contamination in the bulk product used for repackaging. The recall affects 1,391 units distributed across 10 states.
Product
BIOTROL PURIT Clean-It General Purpose Ultrasonic Cleaner, REF PC016, net contents 16 fl. oz., makes 16 gallons of solution.
Category
Medical Device
Distribution
10 states
HighFDA (Food)·F-0020-2025·2024-10-09
Banana nut muffins recalled for undeclared milk and wheat allergens
The Posh Bakery recalls Whole Grains Bakery Banana Nut Muffins (6 oz) due to undeclared milk and wheat allergens. The muffins lack required allergen-contains statements and nutritional fact labels.
Product
Whole Grains Bakery labeled "Banana Nut Muffin", 6 oz. Whole Grains Bon Croissant, Sacramento, CA 95826, (916)-793-0090 UPC"7 13583 05 101 6"
Category
Food
Distribution
0 states
HighFDA (Food)·F-0013-2025·2024-10-09
Big Bottom Milk Chocolate Milk Recalled for Inadequate Pasteurization
Big Bottom Milk Company is recalling 701 units of Chocolate Milk Grade A (1-pint bottles) distributed in Georgia, North Carolina, and South Carolina due to failure to achieve required pasteurization temperatures.
Product
BIG BOTTOM MILK COMPANY, CHOCOLATE MILK GRADE A, 1 US Pint (0.473 liters), Big Bottom Milk Company 221 Hogan Rd, Forest City, NC, Expiration Date 09/09/2024 UPC code 850061506078
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-0009-2025·2024-10-09
BD FACSDuet Sample Preparation System software defect causes inaccurate specimen volumes
The BD FACSDuet sample preparation system may dispense specimen volumes that are 3% to 20% higher in one tube versus another, leading to inaccurate blood counts, delayed test results, and potential additional blood collection. The defect affects 130 systems distributed across the US and internationally.
Product
BD FACSDuet Premium Sample Preparation System, REF: 666340, 666339; and BD FACSDuet Sample Preparation System (Base), REF: 663128, 662588, used with software V 1.4.1. Intended use: to prepare human specimens to be analyzed.
Category
Medical Device
Distribution
13 states
HighFDA (Food)·F-0012-2025·2024-10-09
Big Bottom Milk Company Chocolate Milk Recalled for Inadequate Pasteurization
Big Bottom Milk Company is recalling chocolate milk that was not properly pasteurized. The recall affects 251 units distributed to Georgia, North Carolina, and South Carolina.
Product
BIG BOTTOM MILK COMPANY, CHOCOLATE MILK GRADE A, 1 US Half Gallon (1.89 liters), Big Bottom Milk Company 221 Hogan Rd, Forest City, NC, Expiration Date 09/09/2024 UPC code 850061506054
Category
Food
Distribution
3 states
HighFDA (Food)·F-0005-2025·2024-10-09
Sriracha Sauce Recalled for Manufacturing Without Proper Authorization
Blue Tape Sriracha sauce (136 bottles, 10.5 oz each) was manufactured without the required authorization for producing acidified foods, creating potential safety risks.
Product
Blue Tape Sriracha sauce is refrigerated condiment, packaged in a 10.5oz clear squeeze bottle, sold individually. Ingredients: Chilies, Garlic, Capsicum, Sugar, Salt, White Wine Vinegar. There is no company address on the label and no UPC code.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0007-2025·2024-10-09
Sqwincher Electrolyte Beverage Mix Recalled for Potential Metal Contamination
Kent Precision Foods Group is recalling Sqwincher Electrolyte Beverage Mix in four flavors due to potential metal contamination. The affected powdered beverages were distributed across 11 states.
Product
1. Sqwincher Electrolyte Beverage Mix, orange powder packs, Net Wt 23.83 oz (1 lb 8 oz) 675.6 g: UPC 7588025004; packaged in assorted case, 32 per case / 2.5 gal yield item number 159016044 2. Sqwincher Electrolyte Beverage Mix, grape powder packs, Net Wt 23.83 oz (1 lb 8 oz) 67
Category
Food
Distribution
11 states
HighFDA (Devices)·Z-0019-2025·2024-10-09
Hemodialysis console blood leak sensor may fail to trigger alarm
A component in certain Tablo Hemodialysis consoles may fail to detect small blood leaks promptly, potentially causing symptoms like hypotension, fatigue, and dizziness if undetected blood loss occurs.
Product
Tablo Console, REF: PN-0003000, PN-0006000, part of the Tablo Hemodialysis System. The Tablo Hemodialysis System is indicated for use in patients with acute and/or chronic renal failure, with or without ultrafiltration, in an acute or chronic care facility.
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-0006-2025·2024-10-09
Miami J Select Collar Recalled Due to Adhesive Failure
Ossur is recalling Miami J Select Collars due to pressure-sensitive adhesive hooks that may peel off during repeated use, potentially reducing cervical spine immobilization effectiveness.
Product
Miami J Select Collar, Catalog: MJS-101; Miami J Select Collar Set, Catalog: MJSR-101
Category
Medical Device
Distribution
39 states

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10976–11000 of 31361