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

9276–9300 of 113902

HighFDA (Devices)·Z-1762-2025·2025-05-21
Tornado Embolization Microcoil recalled for incorrectly sized coils
Cook Incorporated is recalling Tornado Embolization Microcoils due to incorrectly sized coils in affected lots. The devices are used for vascular embolization procedures.
Product
Tornado Embolization Microcoil, intended for embolization of selective vessel supply to arteriovenous malformations and other vascular lesions, RPN MWCE-18S-3/2-TORNADO (GPN G08261), RPN MWCE-18S-3/2-TORNADO-081800 (GPN G13102), RPN MWCE-18S-4/2-TORNADO (GPN G08357)
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1768-2025·2025-05-21
KliniTray surgical alignment system recalled for microbial contamination risk
Klinika Medical is recalling the KliniTray tissue resection margin examination board (Model 2001105-F) due to potential microbial contamination. The device was distributed nationwide in Massachusetts.
Product
KliniTray. KlinioTray. Tissue resection margin examination board/small. Model Number: 2001105-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact orientation and posi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0777-2025·2025-05-21
Kasundi Peeled Mango Pickle in Oil recalled for elevated lead levels
Advance Food International Inc. is recalling Kasundi Peeled Mango Pickle in Oil due to elevated lead levels detected in the product. The affected product was distributed in the Northeast.
Product
National brand Kasundi PEELED MANGO PICKLE IN OIL; Net Wt.: 1 Kg (35.27 oz)/ 2.20lb; Ingredients: Kasundi (Peeled Mango), Canola Oil, Cabbage, Salt, Mixed Spices, Vinegar, Sodium Benzoate as preservative; Product of Pakistan; packaged in a plastic jar with a red lid
Category
Food
Distribution
6 states
HighFDA (Food)·F-0767-2025·2025-05-21
Bonya Peach Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Peach Yogurt Parfait (8oz cups) distributed to NY, PA, MA, and NJ due to undeclared almonds that may pose a risk to consumers with tree nut allergies.
Product
Bonya Peach Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
HighFDA (Food)·F-0766-2025·2025-05-21
Bonya Mango Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Mango Yogurt Parfait (8oz) because it contains undeclared almonds, a major food allergen. The product was distributed to NY, PA, MA, and NJ.
Product
Bonya Mango Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-1748-2025·2025-05-21
Abbott Alinity m Resp-4-Plex Amplification Kit Recall
Abbott Molecular is recalling the Alinity m Resp-4-Plex Amplification Kit due to reports of reactive negative controls and false positive results in respiratory virus testing.
Product
Alinity m Resp-4-Plex Amplification (AMP) Kit (CE), List Number 09N79-090, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR) test intended for the qualitative detection and differentiation of RNA from influenza A virus (flu A), influenza B virus (fl
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0801-2025·2025-05-21
New England Village Snacks Mix Recalled for Undeclared Allergens
New England Village Snacks The 19th Hole Snack Mix (5 oz. and 10 oz.) is being recalled due to undeclared almonds and sesame. Consumers with allergies to these ingredients should not consume the product.
Product
New England Village Snacks The 19th Hole Snack Mix (5 oz. and 10 oz.)
Category
Food
Distribution
1 state
HighFDA (Food)·F-0808-2025·2025-05-21
Dixit Foods Sabudana Khichadi Recalled for Undeclared Milk and Peanut Allergens
Dixit Foods Sabudana Khichadi (200 g) is recalled due to undeclared milk and/or peanut allergens. The product may pose a serious risk to consumers with allergies to these ingredients.
Product
Dixit Foods, Sabudana Khichadi, Net Wt. 200 g, Ingredients: Sago (Sabudana), Crushed Groundnuts, Sugar, DesiGhee, Salt, Green Chilli, Cumin Seeds. Allergen Information: May contain Peanuts, Treenuts, Wheat, Sesame, Mustard
Category
Food
Distribution
3 states
HighFDA (Food)·F-0764-2025·2025-05-21
Bonya Vanilla Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Vanilla Yogurt Parfait (8oz) due to undeclared almonds, which pose a risk to consumers with almond allergies. The product was distributed to NY, PA, MA, and NJ.
Product
Bonya Vanilla Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
HighFDA (Food)·F-0765-2025·2025-05-21
Bonya Blueberry Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Blueberry Yogurt Parfait (8 oz) distributed in NY, PA, MA, and NJ because the product contains undeclared almonds, which poses a risk to consumers with tree nut allergies.
Product
Bonya Blueberry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
HighFDA (Food)·F-0786-2025·2025-05-21
Quick Blend Vanilla Flavored Ice Cream recalled for plastic contamination
Wells Enterprises is recalling Quick Blend Vanilla Flavored Ice Cream (3-gallon tubs) because plastic material may be present in the product.
Product
Quick Blend Vanilla Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640050604, Item: 773034
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1779-2025·2025-05-21
Philips Intera 1.5T R11 MRI System Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.5T R11 MRI systems because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could contact patients and cause skin injuries.
Product
Intera 1.5T R11, Model Number: 781170;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1771-2025·2025-05-21
Philips Intera 0.5T Standard MRI System Quadrature Body Coil Seal
Philips is recalling the Intera 0.5T Standard MRI system (Model 781101) because the Quadrature Body Coil seal adhesive may fail and create sharp edges that could injure patients during scanning.
Product
Intera 0.5T Standard, Model Number: 781101;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0781-2025·2025-05-21
Wells Dairy Peanut Butter N Fudge Ice Cream Recall Plastic Foreign Material
Wells Enterprises is recalling Peanut Butter 'N Fudge Ice Cream 3-gallon tubs because plastic foreign material may be present in the product.
Product
Peanut Butter 'N Fudge Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640050574, Item: 33429
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1766-2025·2025-05-21
Centurion Sterile Weitlaner Retractor recalled for sterile packaging puncture risk
Medline Industries is recalling Centurion Sterile Weitlaner Retractor 3 x 4 Prong units because the retractors may puncture through the sterile packaging. The product is distributed nationwide.
Product
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1752-2025·2025-05-21
Pruitt Irrigation Occlusion Catheter Recalled for Incomplete Sterile Seals
LeMaitre Vascular is recalling Pruitt Irrigation Occlusion Catheters (Catalog Numbers 2102-09, E2102-09) due to incomplete sterile barrier seals found during internal testing. The defect affects approximately 26,872 units distributed nationwide and internationally.
Product
Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1769-2025·2025-05-21
KliniTray Platte Faxitron Sterile Tissue Resection Examination Board Recalled
KliniTray Platte Faxitron sterile tissue resection margin examination boards (Model 2001155-F) are being recalled due to potential for microbial contamination. Affected units were distributed nationwide.
Product
KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1775-2025·2025-05-21
Philips Intera 1.5T MRI Scanner Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.5T Explorer/Nova Dual MRI scanners (Model 781108) due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges that could contact patients during scanning and cause skin injuries.
Product
Intera 1.5T Explorer/Nova Dual, Model Number: 781108;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0800-2025·2025-05-21
Ellington Farms Vanilla Flavored Ice Cream Recalled for Plastic
Wells Enterprises, Inc. is recalling Ellington Farms Vanilla Flavored Ice Cream (3-gallon tubs) distributed across the US because plastic material may be present in the product.
Product
Ellington Farms Vanilla Flavored Ice Cream, 3 GAL, DISTRIBUTED BY Ben E. Keith Foods, Fort Worth, TX 76101 UPC: 046045065833, Item: 1144464
Category
Food
Distribution
0 states
HighFDA (Food)·F-0802-2025·2025-05-21
Beijing Soybean Paste Recalled Due to Undeclared Wheat
May Flower International Inc is recalling Beijing Soybean Paste (8.82 oz/250g packages) because the product contains undeclared wheat, posing a risk to consumers with wheat allergies.
Product
Beijing Soybean Paste, packaged in 8.82 ounce/250g red and white packages; Ingredients Soybean, Flour, Salt, Water, Potassium Sorbate; UPC: 6917799000385
Category
Food
Distribution
12 states
HighFDA (Food)·F-0792-2025·2025-05-21
Wells Dairy GFGB Vanilla Ice Cream Recalled for Plastic Contamination
Wells Enterprises is recalling GFGB 12% Vanilla Flavored Ice Cream (3-gallon tubs) because plastic foreign material may be present in the product. Consumers should not consume the product and should contact the company or retailer.
Product
GFGB 12% Vanilla Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640018451, Item: 1435313
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1776-2025·2025-05-21
Philips Intera 1.5T MRI Scanner Body Coil Seal Failure Recall
Philips is recalling 103 Intera 1.5T MRI scanners worldwide because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could cause skin abrasions, bruises, lacerations, hair loss, or tissue injury to patients.
Product
Intera 1.5T Master/Nova, Model Number: 781106;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0778-2025·2025-05-21
President Brand Kumquat Slices Recalled for Undeclared Sulfites
East CK Trading Inc. is recalling President Brand Kumquat Slices because they contain undeclared sulfites. Sulfites are a known allergen that can cause serious reactions in sensitive individuals.
Product
PRESIDENT BRAND; Kumquat Slices; NET WT. 8 OZ/227g; EAST CK TRADING INC.; INGREDIENTS: Kumquat slices; packaged in clear plastic jars with UPC 8 10077 20936 3
Category
Food
Distribution
4 states
HighFDA (Food)·F-0783-2025·2025-05-21
Scooper Hero Ice Cream recalled for possible plastic contamination
Wells Enterprises is recalling Scooper Hero Ice Cream 3-gallon tubs because plastic foreign material may be present in the product.
Product
Scooper Hero Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640050642, Item: 487054
Category
Food
Distribution
0 states
HighFDA (Food)·F-0771-2025·2025-05-21
Bonya Coconut Yogurt Parfait Recalled for Undeclared Almonds
Knockroe Inc is recalling Bonya Coconut Yogurt Parfait (8 oz) distributed to NY, PA, MA, and NJ because it contains undeclared almonds, a common allergen.
Product
Bonya Coconut Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states

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9276–9300 of 113902