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

10801–10825 of 31361

ModerateFDA (Drugs)·D-0025-2025·2024-10-30
Stool Softener Laxative Recalled Due to Manufacturing Practice Deviations
Akron Pharma is recalling OneLAX Docusate Sodium Liquid stool softener due to manufacturing practice deviations. The recall affects 10,845 bottles distributed nationwide.
Product
OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxative, 16 FL OZ (473 mL) bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., Fairfield, NJ 07004, NDC 71399-0039-06.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0021-2025·2024-10-30
Oxytocin Injection Recalled for Current Good Manufacturing Practice Violations
Fresenius Kabi Compounding is voluntarily recalling over 4,400 bags of Oxytocin 0.9% Sodium Chloride Injection due to current Good Manufacturing Practice violations. No illnesses have been reported.
Product
Oxytocin 0.9% Sodium Chloride Injection USP, 30 units per 500 mL Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC: 71506-028-59
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0181-2025·2024-10-30
Olympus Gastrointestinal Videoscope Recalled Due to Incorrect Sensor Color Correction Programming
Olympus Corporation is recalling the Gastrointestinal Videoscope Model GIF-1100 due to incorrect color correction data programmed into CCD imaging sensors. The affected units do not meet device specifications.
Product
Olympus Gastrointestinal Videoscope, Model/Catalog Number: GIF-1100
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0064-2025·2024-10-30
Horizon Organic Ultra Pasteurized Heavy Whipping Cream recalled for potential premature spoilage
Horizon Organic Dairy is recalling approximately 2,956 cases of Ultra Pasteurized Heavy Whipping Cream (BEST BY 10/22/24) distributed across 14 states due to the potential for premature spoilage during shelf life.
Product
Horizon Organic Ultra Pasteurized Heavy Whipping Cream, refrigerated, One Pint (473ml), UPC 7 42365 21685 5. There are 12 cartons per case. Distributed by: Horizon Organic Dairy, LLC (Horizon) Broomfield, CO 80021.UPC: 742365216855
Category
Food
Distribution
14 states
ModerateFDA (Drugs)·D-0019-2025·2024-10-30
Drug Recall: NORepinephrine Injectable Due to Manufacturing Compliance Violations
Fresenius Kabi Compounding recalls 2,151 bags of NORepinephrine Bitartrate injectable due to manufacturing violations. The voluntary recall affects 125 healthcare accounts nationwide.
Product
NORepinephrine Bitartrate 0.9% Sodium Chloride Injection USP, 4 mg per 250 mL, Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC: 71506-025-58
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0014-2025·2024-10-30
Drug injection product recalled due to manufacturing quality violations
Fresenius Kabi Compounding is recalling phenylephrine HCl injection bags due to manufacturing quality violations. The recall affects 1,313 bags distributed to 125 healthcare accounts.
Product
Phenylephrine HCl 0.9% Sodium Chloride Injection USP, 20 mg per 250 mL, Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC 71506-002-58
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0015-2025·2024-10-30
Sterile drug injection bags recalled for manufacturing process violations
Fresenius Kabi Compounding recalled 1,631 bags of Phenylephrine HCl injection due to manufacturing process violations. The product was distributed to 125 healthcare facilities nationwide. The recall was concluded in August 2025.
Product
Phenylephrine HCl 0.9% Sodium Chloride Injection USP, 20 mg per 250 mL, Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC 71506-024-58
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0018-2025·2024-10-30
Vancomycin Injection Recalled Due to Manufacturing Process Violations
Fresenius Kabi Compounding is recalling Vancomycin HCl injectable medication due to cGMP manufacturing violations. The recall affects 1,082 bags distributed to 125 healthcare accounts nationwide.
Product
Vancomycin HCl 750 mg per 250 mL 0.9% Sodium Chloride Injection USP, Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC 71506-014-58
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·25021·2024-10-24
Ricky Powersports ATVs Recalled for Safety Regulation Violations
Ricky Powersports is recalling about 385 youth and adult all-terrain vehicles due to violations of federal ATV safety regulations that pose risks of serious injury or death. The youth ATVs have suspension defects, and the adult ATVs have brake and handlebar safety issues.
Product
Ricky Powersports Tumble Weed Youth and TGB Blade Adult All-Terrain Vehicles (ATVs)
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25019·2024-10-24
CFMOTO 2024 CFORCE All-Terrain Vehicles Recalled for Throttle Failure Crash Hazard
CFMOTO is recalling about 2,650 of its 2024 CFORCE 800 Touring and 2024 CFORCE 1000 Touring ATVs because the throttle lever can fail to return to idle, causing unexpected acceleration and crash risk. One minor injury has been reported.
Product
2024 CFORCE 800 Touring and 2024 CFORCE 1000 Touring All-Terrain Vehicles (ATVs)
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·25020·2024-10-24
PowerBlock Commercial Pro 100 Weight Sets with 5 lb Grip Handles Recalled
PowerBlock is recalling about 1,845 Commercial Pro 100 weight sets sold with 5 lb grip handles because weight plates above 55 lbs can dislodge during use, posing an impact injury risk.
Product
Commercial Pro 100 sold with 5 lb grip handles
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Food)·F-0037-2025·2024-10-23
Nuts.com recalls S'mores Bites for undeclared milk allergen
Nuts.com is recalling S'mores Bites due to undeclared milk allergen. Milk chocolate was listed in the product description but omitted from the ingredient list, creating a labeling mismatch.
Product
S'mores Bites, 1 yummy pound, Distributed by Nuts.com, Cranford, NJ, 07016
Category
Food
Distribution
36 states
SevereFDA (Food)·F-0036-2025·2024-10-23
Enjoy Premium Coconut Cookies Recalled for Undeclared Milk Allergen
KTM Services, Inc. is recalling Enjoy Premium Coconut Cookies sold in Hawaii, Guam, Nevada, and online due to undeclared milk allergen. Consumers with milk allergies should not consume the product.
Product
Enjoy Premium Coconut Cookies packaged in 5.3 oz. foil pouches and 17.7 oz clear bags
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0035-2025·2024-10-23
Enjoy Premium Taro Cookies recalled for undeclared milk allergen
Enjoy Premium Taro Cookies contain undeclared milk allergen and were sold in Hawaii, Guam, and Nevada. Consumers with milk allergies should not consume this product.
Product
Enjoy Premium Taro Cookies packaged in 5.3 oz. foil pouches and 17.7 oz clear bags
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0048-2025·2024-10-23
Seasoned Pepper with Soybean Paste Recalled for Undeclared Allergens
Lemonland Food Corp is recalling Item FLD1020A Seasoned Pepper with Soybean Paste due to undeclared wheat, fish, and crustacean allergens. Consumers with allergies should not consume this product.
Product
Item FLD1020A, Seasoned Pepper with Soybean Paste, distributed in plastic clamshell containers. Net wt. 0.315lb. The H-Mart label declares: Pepper, Soy Bean Paste.
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0038-2025·2024-10-23
Potato Salad Recall: Undeclared Egg and Soybean Allergens
Lemonland Food Corp is recalling potato salad due to undeclared egg and soybean allergens present in the mayonnaise ingredient. The recall affects 120 packages distributed in Washington.
Product
Item FLD4006, Potato Salad, distributed in plastic clamshell containers, net wt. 0.56lb. The H-Mart label declares: Potato, Mayonnaise, Sugar, Vegetable.
Category
Food
Distribution
1 state
SevereFDA (Drugs)·D-0012-2025·2024-10-23
Atovaquone Oral Suspension Recalled for Cohnella Bacteria Contamination
Bionpharma Inc. is recalling Atovaquone Oral Suspension (750 mg/5 mL) nationwide due to Cohnella bacteria contamination. The recall affects 1,980 bottles.
Product
ATOVAQUONE — ATOVAQUONE (ATOVAQUONE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0043-2025·2024-10-23
Seasoned Radish Recalled for Undeclared Crustacean Allergen
Lemonland Food Corp is recalling Item FLD1080A Seasoned Radish due to undeclared shrimp. The product was distributed in Washington; consumers with crustacean allergies should not consume it.
Product
Item FLD1080A, Seasoned Radish, distributed in plastic clamshell containers, net wt. 0.365lb. The H-Mart label declares: Radish, Red Pepper Powder, Malt Syrup, Salt, Anchovy, Sugar, Garlic, Ginger, Sesame.
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0044-2025·2024-10-23
Seasoned Dandelion Recalled for Undeclared Fish Allergen
Lemonland Food Corp is recalling Item FLD1070A Seasoned Dandelion due to undeclared fish (anchovy) not listed on the label. Consumers with fish allergies should not consume this product.
Product
Item FLD1070A, Seasoned Dandelion, distributed in plastic clamshell containers. Net wt. 0.365lb. The H-Mart label declares: Dandelion, Salt, Garlic, Soy Sauce, Chili Powder.
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0046-2025·2024-10-23
Octopus Product Recalled for Undeclared Fish Allergen
Lemonland Food Corp is recalling Item FLD2011 Salted and Seasoned Small Octopus because it contains undeclared fish (anchovy), a major allergen. Approximately 70 packages were distributed in Washington state.
Product
Item FLD2011, Salted and Seasoned Small Octopus, distributed in plastic clamshell containers, net wt. 0.267lb. The H-Mart label declares: Octopus, Salt, Garlic, Ginger, Red Pepper Powder, Green Onion, Syrup, Sesame Seed.
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-0047-2025·2024-10-23
GE HealthCare Giraffe OmniBed neonatal incubator door screw may loosen
Certain GE HealthCare Giraffe OmniBed and Carestation neonatal incubators may have door-securing screws that were not torqued to specification, potentially causing the doors to become loose. These units are distributed worldwide.
Product
GE Heathcare Giraffe OmniBed; neo natal incubator
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·F-0041-2025·2024-10-23
Perilla Leaves in Soy Sauce recalled for undeclared wheat and fish allergens
Lemonland Food Corp recalls Item FLD1000BA Perilla Leaves in Soy Sauce due to undeclared wheat and fish allergens on the label. Consumers with these allergies should not consume the product.
Product
Item FLD1000BA, Perilla Leaves in Soy Sauce, distributed in plastic clamshell containers, net wt. 0.315lb. The H-Mart label declares: Perilla Leaves, Soy Sauce, Sugar
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0119-2025·2024-10-23
Medline Heart CABG Cannulae Recalled Due to Incorrect Model Labeling
Medline Industries is recalling 15 kits of MEDLINE HEART CABG DLP Vessel Cannulae due to incorrect model labeling discovered during manufacturing.
Product
MEDLINE HEART CABG CDS, REF CDS983376R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0085-2025·2024-10-23
Leica Cryostat Model CM1100 Recalled for Fire Risk from Flammable Freezing Sprays
Leica Biosystems recalls its Cryostat Model CM1100 due to inadequate warnings about using flammable freezing sprays, which can ignite and cause serious injuries. The device labeling lacked required safety warnings prior to 2019.
Product
Leica Biosystems Cryostat Model Number CM1100, Material Number 14046931130, for freezing and sectioning tissue samples
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0101-2025·2024-10-23
AVVIGO+ Medical Imaging System Grid Overlay Display Software Error
Boston Scientific is recalling AVVIGO+ Multi-Modality Guidance Systems due to a software anomaly that displays a 9-grid overlay instead of the correct 15-grid overlay during Live and Record modes. This incorrect display could affect imaging measurements during procedures.
Product
Boston Scientific AVVIGO+ Multi-Modality Guidance System, AVVIGO + MOB SYSTEM - ZERO COST EU + RO; the system utilizes an interactive display to provide physicians with physiologic, intravascular and/or intracardiac anatomical information. The system can provide various modalitie
Category
Medical Device
Distribution
Distributed nationwide

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10801–10825 of 31361