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

7076–7100 of 7514

SevereFDA (Drugs)·D-0023-2022·2021-10-27
AirDuo Digihaler 55/14 Inhalation Powder Recalled for Subpotent Dose
Teva Pharmaceuticals is recalling AirDuo Digihaler 55/14 inhalation powder due to subpotent emitted dose of salmeterol. Approximately 1,978 inhalers distributed nationwide may deliver less medication than labeled.
Product
AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva Respiratory, LLC Frazer, PA 19355, Manufactured in Ireland, NDC 59310-111-06
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0056-2022·2021-10-27
Roasted Salted Cashew Halves and Pieces Recalled for Glass Contamination
Suntree Snack Foods, LLC is recalling 32 oz. jars of Roasted Salted Cashew Halves and Pieces because the product may contain glass pieces. Consumers who have purchased the affected product should stop consuming it.
Product
Roasted Salted Cashew Halves and Pieces, 32 oz. , UPC 072036734907. 6 jars/case.
Category
Food
Distribution
11 states
SevereFDA (Food)·F-0021-2022·2021-10-27
Kalona Supernatural Organic Half & Half Recalled for Improper Pasteurization
Farmers' All Natural Creamery LLC is recalling Kalona Supernatural Organic Half & Half in 16 FL OZ and 32 FL OZ bottles because the product was shipped without being properly pasteurized, creating a food safety risk.
Product
Kalona Supernatural Organic Half & Half, Manufactured in Iowa for Kalona Organics, LLC. Kalona IA in 16 FL OZ (UPC 8-81245-12516-7, 8 bottles per case) and 32 FL OZ (UPC 8-81245-12532-7, 6 bottles per case)
Category
Food
Distribution
7 states
SevereNHTSA·21V837000·2021-10-25
2020-2023 IC Bus School Buses Recalled for Engine Shut Down Risk
Navistar is recalling 2020-2023 IC Bus CESB school buses due to an engine control module defect that may cause unexpected engine shutdown while driving, increasing the risk of crashes and emergency evacuation situations.
Product
IC BUS — 2023 IC BUS CESB
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·22007·2021-10-22
Walmart Better Homes and Gardens Room Spray Recalled for Dangerous Bacteria
Walmart is recalling Better Homes and Gardens Essential Oil Infused Aromatherapy Room Spray with Gemstones due to contamination with Burkholderia pseudomallei bacteria. CDC testing identified the hazard and is investigating a cluster of four melioidosis cases, including two deaths.
Product
Better Homes and Gardens Essential Oil Infused Aromatherapy Room Spray with Gemstones
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·21V830000·2021-10-22
2021-2022 Forest River XLR Toy Hauler Recalled for Missing Furnace Protective Panel
Forest River is recalling certain 2021-2022 XLR Toy Hauler recreational vehicles with a missing protective panel between the furnace and cargo area. The missing panel could allow cargo to contact furnace wiring, creating a fire hazard.
Product
FOREST RIVER — 2022 FOREST RIVER XLR TOYHAULER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0015-2022·2021-10-20
Frozen vegan crabcakes recalled for undeclared egg allergen
Cuisine Innovations Unlimited, LLC is recalling Vemondo Vegan Crabless Mini Crabcakes sold at Lidl due to undeclared egg. The product may pose a risk to consumers with egg allergies.
Product
Vemondo Vegan Crabless Mini Crabcakes by Lidl 8.5 OUNCES (240g) coated paper box ten (10) packages per case. Frozen.
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-0068-2022·2021-10-20
Ultrasound gel products recalled for potential bacterial contamination
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. Products distributed nationwide in the U.S., Canada, and other locations have been recalled.
Product
ECO 50TS Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0008-2022·2021-10-20
Abbott Respiratory Diagnostic Kit Recalled for Potential False Positive Results
Abbott Molecular is recalling the Alinity m Resp-4-Plex AMP Kit due to potential false positive results. The recall affects 5,855 units distributed worldwide.
Product
Alinity m Resp-4-Plex AMP Kit (Non-US Assay) and Alinity m Resp-4-Plex Application Specification File. in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0088-2022·2021-10-20
Eco-Med Ultrasound Gel Recalled for Bacterial Contamination Risk
Eco-Med Pharmaceutical's ultrasound gel products are recalled due to potential bacterial contamination. The FDA advises healthcare providers to stop using the affected product.
Product
EcoGel 200 - RED Medical Supplies Blue Ultrasound Gel, Model No. 250UG-BMU
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0090-2022·2021-10-20
FDA Recalls Ultrasound Gel for Possible Bacterial Contamination
Red Medical Supplies is recalling EcoGel 100 ultrasound gel due to possible bacterial contamination. Approximately 639 units were sold nationwide through Amazon.com.
Product
EcoGel 100 - RED Medical Supplies Green Ultrasound Gel, Model No. 250UG-GLU
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0089-2022·2021-10-20
FDA recalls Eco-Med ultrasound gels due to bacterial contamination risk
FDA recalls ultrasound gels manufactured by Eco-Med Pharmaceutical due to possible bacterial contamination. Healthcare providers and facilities should stop use immediately.
Product
EcoGel 200 - RED Medical Supplies Clear Ultrasound Gel, Model No. 250UG-CMU
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0067-2022·2021-10-20
FDA Recalls Ultrasound Gels and Lotions for Potential Bacterial Contamination
Ultrasound gels and lotions from National Distribution & Contracting Inc are being recalled due to potential bacterial contamination. About 25,103 units distributed nationwide and in Canada are affected.
Product
ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Ultrasound Transmission Clr 8.5 oz BTL 24/cs ECO 40JMC Gel Ultrasound Transmission Clr 5L 4/cs NDC P301008 ProAdvantage Gel Ultrasound Transmission 8.5 oz 12/cs NDC P301105 ProAdvantage Gel Ultrasound Transmission 5 Liter
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0006-2022·2021-10-20
Abbott Alinity m SARS-CoV-2 Amp Kit Recalled for Potential False Positive Results
Abbott Molecular has recalled 71,314 units of the Alinity m SARS-CoV-2 Amp Kit due to potential false positive results. The kit was distributed worldwide.
Product
Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m SARS-CoV-2 Application Specification File. in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0004-2022·2021-10-20
Abbott SARS-CoV-2 Diagnostic Kit Recalled for Risk of False Positive Results
Abbott Molecular is recalling 60,563 units of the Alinity m SARS-CoV-2 Amp Kit due to potential false positive test results. The affected kits were distributed worldwide from September 2021 through January 2023.
Product
Alinity m SARS-CoV-2 Amp Kit (Emergency Use Authorization, US Assay) and Alinity m SARS-CoV-2 Application Specification File. in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0007-2022·2021-10-20
Potassium Chloride Injection Recall Due to Sterility Assurance Lack
SSM Health Care St. Louis is recalling 385 bags of Potassium Chloride 40 mEq in 0.9% Sodium Chloride injection due to lack of assurance of sterility. The affected lot was distributed in Missouri.
Product
Potassium Chloride 40 mEq in 0.9% Sodium Chloride 270 mL NS, 250 mL bag, Rx Only, SSM Health Care Corporation, 1015 Bowles, Fenton, MO. NDC 60652-6429-1
Category
Drug
Distribution
1 state
SevereFDA (Devices)·Z-0007-2022·2021-10-20
Abbott Alinity m SARS-CoV-2 Test Kit Recalled for Potential False Positives
Abbott Molecular recalls its Alinity m SARS-CoV-2 Amp Kit (Non-US Assay), an in vitro diagnostic test, due to potential for false positive results. Approximately 11,408 units were distributed worldwide.
Product
Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m SARS-CoV-2 Application Specification File. in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0005-2022·2021-10-20
Abbott Alinity m Resp-4-Plex Respiratory Diagnostic Kit Recalled for False Positive Results
Abbott is recalling the Alinity m Resp-4-Plex AMP Kit, an in vitro diagnostic used for respiratory pathogen testing, due to potential for false positive results affecting approximately 8,469 units distributed worldwide.
Product
Alinity m Resp-4-Plex AMP Kit (Emergency Use Authorization, US Assay) and Alinity m Resp-4-Plex Application Specification File. in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0009-2022·2021-10-20
Glucagon Emergency Kit Recall: Subpotent Drug in Vials
Eli Lilly is recalling Glucagon Emergency Kits (Lot #D239382D, expiration April 2022) because some vials contain liquid instead of powder and do not deliver the full expected drug effect when administered.
Product
Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection, 1 mg per vial; Diluent for Glucagon, 1 mL syringe. Rx only, Marketed by: Lilly USA, LLC, Indianapolis, IN 46285; Glucagon, NDC: 0002-8031-01
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V822000·2021-10-19
Newmar Motorhomes Power Steering Pump Defect Recall
Newmar is recalling 2020-2022 Essex, King Aire, and London Aire motorhomes due to a power steering pump machining defect that can result in loss of steering assist and increased crash risk. Affected owners should contact Newmar for free inspection and replacement.
Product
NEWMAR — 2020 NEWMAR ESSEX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V817000·2021-10-18
Chevrolet Traverse Wheelchair Accessible Vehicles Recalled for Transmission Fluid Leak Hazard
Braun recalls 2020-2021 Chevrolet Traverse wheelchair vehicles for a transmission fluid leak hazard. A faulty screw and clip may cause fluid loss, risking power loss, crashes, and fire.
Product
CHEVROLET — 2020 CHEVROLET TRAVERSE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V812000·2021-10-15
2021 Volkswagen Atlas front wheel bearing bolts may loosen and cause crash risk
Volkswagen is recalling certain 2021 Atlas, Atlas Cross Sport, and Passat vehicles because the front wheel bearing bolts may have been incorrectly tightened and could loosen, potentially causing loss of control and crash risk.
Product
VOLKSWAGEN — 2021 VOLKSWAGEN ATLAS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V805000·2021-10-15
Ford vehicles recalled for damaged side impact airbag sensors
Ford is recalling certain 2022 and 2021 model vehicles due to damaged side impact airbag sensors that may fail to deploy properly in a crash.
Product
FORD — 2022 FORD F-250 SD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V798000·2021-10-14
RAM Pickup and Cab Chassis Trucks: Intake Heater Relay Fire Risk
Certain 2021-2022 RAM pickup and cab chassis trucks with Cummins diesel engines may experience electrical shorts in the Intake Heater Grid Relay, causing a fire hazard. Owners should park outside until dealers inspect and repair the defect.
Product
RAM — 2022 RAM 4500
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0029-2022·2021-10-13
Eco-Med Ultrasound Gels and Lotions Recalled for Bacterial Contamination
Eco-Med Pharmaceutical's ultrasound gels and lotions are recalled for potential bacterial contamination. The FDA advises health care providers to stop using all affected products.
Product
Action De Gala, FuSion Conductive Gel - Product Usage: Intended for use in acoustic coupling of ultrasound transducer to tissue.
Category
Medical Device
Distribution
Distributed nationwide

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7076–7100 of 7514