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

4151–4175 of 6137

CriticalFDA (Drugs)·D-0066-2023·2022-11-23
Hand Sanitizer Recalled for Methanol Contamination — FDA Class I
Adam's Polishes ALCOHOL BASED HAND SANITIZER (multiple sizes) is recalled nationwide because FDA analysis found methanol contamination. This Class I recall poses a serious chemical health risk.
Product
Adam's Polishes ALCOHOL BASED HAND SANITIZER, isopropyl alcohol 75% v/v, packaged in a) 4 fl. oz (118) spray bottle, NDC 74943-125-04; b) 8 fl. oz (237 mL) spray bottle, NDC 74943-125-08; c) 1 PINT / 16 fl. oz (475 ml.) spray bottle, NDC 74943-125-16; and d) 1 GALLON / 128 fl. oz
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V869000·2022-11-23
International and IC Bus vehicles recalled for defective suspension and steering fasteners
Navistar is recalling certain 2021-2023 International trucks and IC Bus vehicles because hex flange lock nuts in suspension and steering joints were improperly heat treated and may lose tension, creating a risk of steering instability.
Product
INTERNATIONAL — 2023 INTERNATIONAL HV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V873000·2022-11-23
2022 Chevrolet Silverado 1500 Air Bag System Defect Recall
General Motors is recalling 5 2022 Chevrolet Silverado 1500 vehicles due to a manufacturing defect that left the air bag sensing diagnostic module in manufacturing mode. The module was not activated at the assembly plant, meaning air bags will not deploy in a crash.
Product
CHEVROLET — 2022 CHEVROLET SILVERADO 1500
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0151-2023·2022-11-23
Zingerman's Pumpkin Gelato Recalled for Undeclared Egg Allergen
Zingerman's Creamery is recalling Harvest Pumpkin Gelato due to undeclared egg allergen. The recall affects pints and quarts distributed in Michigan.
Product
Zingerman's Harvest Pumpkin Gelato pint (16oz) and quart (32oz) sizes
Category
Food
Distribution
1 state
SevereNHTSA·22V866000·2022-11-23
2022 Dodge Charger Transmission Shifter Assembly Defect Recall
Chrysler is recalling the 2022 Dodge Charger for shifter assembly defects. An improperly heat-treated shifter may slip out of drive position, causing sudden loss of power and increasing crash risk.
Product
DODGE — 2022 DODGE CHARGER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V870000·2022-11-23
2023 IC Bus Models Suspension and Steering Fastener Recall
Navistar is recalling 2023 IC Bus EV, CE, and RE models due to improperly heat-treated fasteners in suspension and steering joints. These fasteners may lose tension and cause steering instability, increasing crash risk.
Product
IC BUS — 2023 IC BUS EV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V865000·2022-11-23
Jeep Wrangler engine shutdown from loss of communication
Certain 2021-2023 Jeep Wrangler 4xe vehicles may experience engine shutdown due to communication loss, reducing drive power and increasing crash risk.
Product
JEEP — 2023 JEEP WRANGLER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0152-2023·2022-11-23
Zingerman's Paw Paw Gelato recalled for undeclared egg allergen
Zingerman's Creamery is recalling Paw Paw Gelato in pint (16 oz) and quart (32 oz) sizes due to undeclared egg. Consumers with egg allergies should not consume this product.
Product
Zingerman's Paw Paw Gelato pint (16oz) and quart (32oz) sizes
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-0154-2023·2022-11-23
Omnipod Dash PDM Insulin Pump Remote Recalled for Battery Fire Hazard
Insulet Corporation is recalling the Omnipod Dash PDM remote controller for insulin pumps due to battery defects causing overheating, swelling, and fire hazard. A fire incident has been reported.
Product
18239: ASM Omnipod Dash PDM, insulin delivery system. PT-000010: Assembly, Dash Final PDM U100, mg/dL PT-000011: Assembly, Dash Final PDM U100, mmol/L PT-000030: Assembly, DASH PDM, Canada Remote Controller (Personal Diabetes Manager or PDM) associated with Insulin Pump (
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22V861000·2022-11-21
Audi vehicles recalled for gateway control module failure causing engine power loss
Volkswagen Group is recalling 2019-2022 Audi sedans, wagons, and allroad models. Liquid in the rear seat may penetrate and shut down the gateway control module, suddenly reducing engine power and increasing crash risk.
Product
AUDI — 2021 AUDI RS7
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·23710·2022-11-17
Polaris Snowmobiles Recalled Due to Fire Hazard from Fuel Tank
Polaris is recalling approximately 138,000 snowmobiles from model years 2013–2023 because electrostatic discharge inside the fuel tank can cause vapors to ignite, leading to tank burst and fire. The firm has received 30 reports of tank bursting, including 16 fires and one burn injury.
Product
Model Year 2021-2023 MATRYX, 2015-2022 AXYS, and 2013-2014 Pro-Ride Snowmobiles
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0058-2023·2022-11-16
Octreotide Acetate Injection Recalled for Glass Particle Contamination
Viatris Inc is recalling Octreotide Acetate Injection due to glass particles found in syringes. Approximately 22,400 syringes of lot #AJ21002 (expiration 03/2024) were distributed nationwide.
Product
OCTREOTIDE ACETATE — OCTREOTIDE ACETATE (OCTREOTIDE ACETATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0226-2023·2022-11-16
Medical Device Procedure Kits Recalled for Foreign Body Reaction Risk
Boston Scientific recalls ORISE ProKnife Procedure Kits due to higher incidence of foreign body reactions to remnant gel post-procedure, which have required surgical intervention in affected patients.
Product
ORISE ProKnife Procedure Kits: indicated for use in gastrointestinal endoscopic procedures for submucosal lift of polyps, adenomas, early stage cancers or other gastrointestinal mucosal lesions, prior to excision with a snare or other suitable endoscopic device.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0225-2023·2022-11-16
ORISE Gel Syringe Recall Due to Foreign Body Reaction Risk
Boston Scientific has recalled ORISE Gel Syringe kits used in gastrointestinal endoscopy due to higher incidence of foreign body reactions from remnant gel requiring surgical intervention.
Product
ORISE Gel Syringe Submucosal Lifting Agent Kits: indicated for use in gastrointestinal endoscopic procedures for submucosal lift of polyps, adenomas, early-stage cancers or other gastrointestinal mucosal lesions, prior to excision with a snare or other suitable endoscopic device
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0147-2023·2022-11-16
Whole Foods Market dipping caramel recalled for undeclared wheat allergen
Whole Foods Market Dipping Caramel (PLU 34888) is recalled because it contains wheat that was not declared on the label. Consumers with wheat allergies should not consume this product.
Product
Whole Foods Market Dipping Caramel, PLU 34888 sold by the pound and packaged in nonflexible plastic containers
Category
Food
Distribution
3 states
SevereFDA (Food)·F-0146-2023·2022-11-16
Hammond's Salted Caramel Cookies Recalled for Undeclared Peanut Allergen
Hammond's Salted Caramel Cookies contain an undeclared peanut allergen due to mispacking of Peanut Butter Chocolate Chip Cookies into Salted Caramel boxes. Nationwide distribution affected.
Product
Hammond's Salted Caramel Cookies, NET WT. 5 OZ (142g), UPC 6 91355 89889 5, Manufactured for: Hammond's Candies, 5735 Washington St, Denver, CO 80216. Cookies are packaged in sealed, opaque, white, plastic bag, which is packed inside printed on cardstock box. There are 8 boxes /c
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0223-2023·2022-11-16
Neonatal Endotracheal Tube Grip with Detachable Metal Clips Recalled
CooperSurgical is recalling NEO-fit Neonatal Endotracheal Tube Grips due to metal clips that can become loose or detach. Eleven complaints include three cases of clip ingestion, three removals from the mouth, and one throat laceration.
Product
NEO-fit Neonatal Endotracheal Tube Grip, Part Number 42-2540
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0138-2023·2022-11-16
Vegan Golden Nuggets recalled for undeclared egg allergen
DA CHENG VEGETARIAN FOOD INC. recalls Vegan Golden Nuggets for containing undeclared egg. The product was distributed to restaurants and retail stores in Utah, Virginia, Texas, and California.
Product
Vegan Golden Nuggets, (6.6 lb bags) Ingredients: (NON GMO) Textured Soybean Fiber, Isolated Soy Protein, Soybean Oil, Sugar, Salt, Pepper, Vegan Chicken Flavor Seasoning (Food Additive: Modified Starch Seasoning, Yeast Extract (Yeast Extract, Salt, Water), Crisp Powder, Bread Pow
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0137-2023·2022-11-16
Vegan Drumsticks Recalled Due to Undeclared Egg Allergen
DA CHENG VEGETARIAN FOOD INC. is recalling Vegan Drumsticks because they contain egg that is not declared on the label. The product poses a risk to consumers with egg allergies.
Product
Vegan Drumsticks, 6.6 lb. bags. Ingredients: (NON GMO) Textured Soybean Fiber, Isolated Soy Protein, Soybean Oil, Sugar, Salt, Pepper Spice, Vegan Seasoning Keep Frozen
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0148-2023·2022-11-16
ReadyMeals Chicken Salad Quad Recalled for Undisclosed Tree Nut Allergen
ReadyMeals Chicken Salad Quad products distributed in CO, NE, NM, SD, and WY have labels missing tree nut (cashew) allergen information. Consumers with tree nut allergies should not consume this product.
Product
ReadyMeals Chicken Salad Quad, 12 oz., in a clear plastic container with four compartments, UPC 2 1352 40000 0, Distributed by: Safeway Inc., Pleasanton, CA 94588. Perishable - Keep Refrigerated
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0139-2023·2022-11-16
Vegan Golden Nuggets recalled for undeclared egg allergen
DA CHENG VEGETARIAN FOOD INC. recalls Vegan Golden Nuggets due to undeclared egg allergen. The product is marketed as vegan but contains egg, which is not declared on the label.
Product
Vegan Golden Nuggets, (1 lb. bags) Ingredients: (NON GMO) Textured Soybean Fiber, Isolated Soy Protein, Soybean Oil, Sugar, Salt, Pepper, Vegan Chicken Flavor Seasoning (Food Additive: Modified Starch Seasoning, Yeast Extract (Yeast Extract, Salt, Water), Crisp Powder, Bread Pow
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-0224-2023·2022-11-16
Medical Device Recall: ORISE Gel Submucosal Lifting Agent Due to Foreign Body Reactions
Boston Scientific is recalling ORISE Gel Submucosal Lifting Agent due to higher incidence of foreign body reactions to retained gel. These reactions caused mass formations requiring surgical intervention.
Product
ORISE Gel Submucosal Lifting Agent--Indicated for use in gastrointestinal endoscopic procedures for submucosal lift of polyps, adenomas, early stage cancers or other gastrointestinal mucosal lesions, prior to excision with a snare or other suitable endoscopic device Packaged as
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0149-2023·2022-11-16
Chicken Salad Sandwich Club 18 Inch Tray Recalled for Undisclosed Cashew Allergen
Albertsons Companies LLC is recalling Chicken Salad Sandwich Club trays because labels fail to disclose tree nuts (cashews) in the ingredient and contains statements. Consumers with cashew allergies may unknowingly consume these sandwiches.
Product
Chicken Salad Sandwich Club 18 Inch Tray, Black tray with 16 pre-made sandwiches, UPC 2 9615 90000 0, Distributed by: Safeway Inc., Pleasanton, CA 94588. Perishable - Keep Refrigerated.
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0136-2023·2022-11-16
Bombolo Biscotti Italian Cookies Recalled for Undeclared Walnut Allergen
Sotto i Trulli is recalling Bombolo Biscotti Assorted Italian Cookies due to undeclared walnut allergen. Consumers with walnut allergies should not consume this product.
Product
Bombolo Biscotti, Assorted Italian Cookies, Net WT. 16 oz (454g)
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0135-2023·2022-11-16
H-E-B Meal Simple Tomato Basil Soup recalled for undeclared milk allergen
Bakkavor USA is recalling H-E-B Meal Simple Tomato Basil Soup due to an undeclared milk allergen that poses a risk to consumers with milk allergies.
Product
H-E-B Meal Simple Tomato Basil Soup 32 oz. Plastic containers, 6 containers per case Keep Refrigerated.
Category
Food
Distribution
1 state

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4151–4175 of 6137