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

24726–24750 of 26084

HighFDA (Devices)·Z-2331-2021·2021-09-01
FDA Recalls AltiVate Shoulder Implant System Due to Component Mating Failure
The FDA is recalling AltiVate Anatomic Shoulder Systems due to humeral stem components that may fail to mate properly with broach handles, potentially delaying surgery or requiring revision.
Product
AltiVate Anatomic Shoulder System for the following Part Numbers: 1. Part # 520-08-00, Rev. C., 2. Part # 520-10-000, 3. Part # 520-12-000, 4. Part # 520-14-000, 5. Part # 520-16-000
Category
Medical Device
Distribution
35 states
HighFDA (Devices)·Z-2349-2021·2021-09-01
Vascular Ultrasound Examination Table Recalled for Weld Failure
Oakworks vascular ultrasound examination tables (models USV1 and USV2) are recalled due to potential weld failure in the tilting mechanism bracket. A failed weld could prevent the table from tilting, affecting patient positioning.
Product
Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowler (USV2). Intended Use: Vascular Ultrasound examination table Catalog Number: 66783 and 64219
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2350-2021·2021-09-01
Terumo Advanced Perfusion System Electronic Patient Gas System Recalled for Control Failure
The Terumo Advanced Perfusion System 1 Electronic Patient Gas System is recalled for intermittent initialization failures that disable the primary control interface, requiring use of backup local controls.
Product
Terumo Advanced Perfusion System 1 Electronic Patient Gas System Catalog #: 801188
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2337-2021·2021-09-01
ECHELON MRI System Recalled for Missing Natural Rubber Allergen Labeling
Hitachi Healthcare Americas is recalling ECHELON MRI System table pads because packaging and user manuals lack required disclosure that the pads contain dry natural rubber, a potential allergen. No illnesses have been reported.
Product
ECHELON MRI System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2342-2021·2021-09-01
Philips Ingenia MRI System recalled due to incorrect pressure relief valve
Philips recalled 27 units of the Ingenia 1.5T Magnetic Resonance system with an incorrect pressure relief valve (42 psi instead of 3.75 psi) that could release helium gas and cause injury.
Product
Ingenia 1.5T-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body or extremities Model Number: 7
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2338-2021·2021-09-01
MRI System Table Pads Missing Required Natural Rubber Allergen Label
Table pads in Hitachi's ECHELON Oval MRI System contain natural rubber but lack required labeling on packaging and in user manuals. Federal regulations under 21 CFR 801.437 mandate disclosure of this material.
Product
ECHELON Oval MRI System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2346-2021·2021-09-01
MRI System Pressure Relief Valve Defect May Cause Helium Release
Philips Achieva 3.0T MRI systems may have an incorrectly installed pressure relief valve that could release helium gas and cause injury. Affected units are distributed in the United States and internationally.
Product
Achieva 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body or extremities Model Number: 7
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0886-2021·2021-09-01
Assist and Amend Digestive Enzyme Formula Dietary Supplement Recall—Undeclared Allergens
New Dawn Nutrition is recalling Assist and Amend Advanced Digestive Enzyme Formula (Lot #361551, Best By 2022) because it contains undeclared milk, wheat, and soy. Consumers with allergies to these substances are at risk of allergic reaction.
Product
Assist and Amend Advanced Digestive Enzyme Formula, Dietary Supplement, 60 capsules per bottle, Manufactured for and distributed by New Dawn Nutrition Omaha, NE
Category
Food
Distribution
0 states
HighCPSC·21193·2021-09-01
TurboSke Kids Toddler Bike Helmets Recalled for Head Injury Risk
SKE Outdoors is recalling about 860 TurboSke Kids Toddler Bike Helmets (size small) because they do not meet U.S. CPSC federal safety standards, posing a risk of head injury. No injuries have been reported.
Product
TurboSke Kids Toddler Bike Helmets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0887-2021·2021-09-01
Crunchmaster Gluten-Free Crackers Recalled for Possible Glass
TH Foods Inc is recalling Crunchmaster Multi Grain Baked Gluten-Free Crackers due to possible pieces of glass in the product. The recall affects 7,056 retail units sold in Iowa, Illinois, Indiana, Minnesota, and Wisconsin.
Product
Crunchmaster Multi Grain Baked Gluten-Free Crackers 5-Seed Sesame, Amaranth, Flax, Chia & Quinoa 20 oz. UPC Code: 8-79890-00220-9
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-2354-2021·2021-09-01
Accu-Chek Inform II glucose test strips may open during shipment
Roche Diabetes Care is recalling Accu-Chek Inform II glucose test strips because vials may open during shipment, exposing strips to humidity and potentially causing inaccurate test results.
Product
Accu-Chek Inform II Test Strip, Whole Blood Glucose Test System, Model number 05942891001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2343-2021·2021-09-01
Diagnostic MRI system recalled for pressure relief valve defect
A Philips Ingenia MRI system has been recalled due to installation of a 42 psi pressure relief valve instead of the correct 3.75 psi valve, which may result in helium gas release and injury.
Product
Ingenia 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body or extremities Model Number: 7
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2352-2021·2021-09-01
Accu-Chek Performa Test Strips Recalled Due to Defective Packaging
Roche Diabetes Care is recalling Accu-Chek Performa test strips because vials may open during shipment, exposing strips to humidity and causing inaccurate glucose readings that could lead to inappropriate diabetes treatment decisions.
Product
Accu-Chek Performa Test Strip, Blood Glucose Monitoring System, Model number 07299702001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2356-2021·2021-09-01
Surgical Shears HARMONICHD 1000i Recalled Due to Component Defect and Burn Risk
Ethicon is recalling HARMONICHD 1000i Shears due to a cracked internal component that may cause continuous device activation and result in burns. About 68,960 units have been distributed worldwide.
Product
HARMONICHD 1000i Shears (36cm Shaft Length)-indicated for soft tissue incisions when bleeding control and minimal thermal injury are desired. Product Code: HARHD36
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2344-2021·2021-09-01
Philips Ingenia MRI System Equipped With Incorrect Pressure Relief Valve
Philips Ingenia Elition X MRI systems contain an incorrectly installed pressure relief valve that may release helium gas and cause injury. The recall affects 6 U.S. units and 12 units distributed internationally.
Product
Ingenia Elition X-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body or extremities Model Numb
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V677000·2021-08-31
Power Steering Pump Defect in 2021 Autocar Xpeditor Vehicles
Autocar is recalling 2021 Xpeditor and certain 2020-2021 Legend vehicles due to a power steering pump defect that can cause loss of power steering assist and increase crash risk.
Product
AUTOCAR — 2021 AUTOCAR XPEDITOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V675000·2021-08-30
2021 Subaru Impreza recalled for suspension control arm failures
Subaru is recalling 2021 Impreza vehicles because the left-front lower control arm weld may fail, causing the arm to separate. This could result in loss of vehicle control and increased crash risk.
Product
SUBARU — 2021 SUBARU IMPREZA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V671000·2021-08-27
2021 Airstream RVs Recalled for Propane Regulator Failure Fire Risk
Airstream is recalling certain 2021 recreational vehicles with propane regulator defects that can increase pressure and enlarge flames in gas appliances, creating a fire risk. Dealers will replace the regulator and test the system at no cost.
Product
AIRSTREAM — 2021 AIRSTREAM GLOBETROTTER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V670000·2021-08-27
KZRV recreational vehicles recalled for faulty propane regulators
KZRV is recalling 2018-2022 recreational vehicles with defective Winntec propane regulators that may fail and increase pressure, raising the risk of fire.
Product
KZRV — 2020 KZRV SPORTSMEN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V663000·2021-08-26
Coach House Platinum II recreational vehicle window adhesive failure recall
Coach House is recalling 2019-2022 Platinum II and 2022 Platinum recreational vehicles due to window adhesive failure. The adhesive bonding the window vent may fail, potentially causing detachment and increasing crash or injury risk.
Product
COACH HOUSE — 2021 COACH HOUSE PLATINUM II
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V668000·2021-08-26
Land Rover seat belt retractor defect affects child restraint security
Land Rover is recalling certain 2020-2022 vehicles because the seat belt automatic locking retractors may deactivate early, preventing child restraint systems from securing properly. This can increase the risk of injury during a crash.
Product
LAND ROVER — 2021 LAND ROVER DEFENDER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V664000·2021-08-26
2021 Dodge Challenger Safety System Status Indicators May Not Illuminate Properly
2021 Dodge Challenger vehicles may not properly illuminate safety system status indicators in daylight or nighttime conditions. This could prevent drivers from knowing the status of vehicle safety systems, increasing crash risk.
Product
DODGE — 2021 DODGE CHALLENGER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0737-2021·2021-08-25
Leucovorin Calcium Injection Recalled Due to Sterility Concerns
Teva Pharmaceuticals is recalling Leucovorin Calcium for Injection (350 mg/vial) distributed nationwide because the manufacturer cannot assure the product meets sterility standards.
Product
Leucovorin Calcium for Injection, USP 350 mg/vial, 17.5 mL single-use vials, Rx only, Teva Parenteral Medicines, Inc. Irvine, CA 92618, NDC 0703-5145-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0731-2021·2021-08-25
Methylprednisolone Acetate Injectable Suspension Recall: Sterility Assurance
Teva Pharmaceuticals USA is recalling Methylprednisolone Acetate Injectable Suspension USP 40 mg/mL in single-dose and multi-dose vials nationwide due to lack of assurance of sterility.
Product
Methylprednisolone Acetate Injectable Suspension USP, 40 mg/mL, packaged in a) 1 mL Single-Dose vials (0703-0031-01), and b) 5mL Multi Dose Vials (NDC 0703-0043-01), and c) 10 mL Multi-Dose Vials (NDC 0703-0045-01), Rx only, TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0733-2021·2021-08-25
Amikacin Sulfate Injection Recalled Due to Sterility Assurance Failure
Teva Pharmaceuticals USA is recalling Amikacin Sulfate Injection USP 1 gram/4mL vials nationwide due to lack of assurance of sterility. The recall affects 4,712 vials with lot #31329243B and expiration date 05/2022.
Product
Amikacin Sulfate Injection USP 1 gram/4mL (250mg/ML), 4 mL single-dose vials, Rx only, Teva Pharmaceuticals USA Inc. North Wales, PA 19454, NDC 0703-9040-01
Category
Drug
Distribution
Distributed nationwide

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