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

351–375 of 36488

SevereFDA (Devices)·Z-2712-2026·2026-07-15
Elekta Geneva Brachytherapy Applicator Intrauterine Tube Detachment Risk
Elekta is recalling the Geneva Brachytherapy Applicator due to a safety concern that the tip of the intrauterine tube may detach and remain inside a patient during cancer treatment.
Product
Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The device is intended for intracavitary brachytherapy for cancer treatment of the cervix and the endometrium. Optional needles can be placed for interstitial therapy.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2711-2026·2026-07-15
Brachytherapy Applicator Advanced Gynecological Applicator Tip Detachment
Elekta, Inc. is recalling Advanced Gynecological Applicators due to potential detachment of the intrauterine tube tip, which may remain inside a patient during cancer treatment.
Product
Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator Product Description: The intended use of the Advanced Gynecological Applicator is intracavitary brachytherapy for cancer treatment of the cervix and endometrium. Optional needles can be placed
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0671-2026·2026-07-15
Pemetrexed for Injection Recalled Due to Lack of Sterility Assurance
Somerset Therapeutics is recalling Pemetrexed for Injection 100mg/Vial due to lack of sterility assurance. The recall affects approximately 12,000 vials distributed nationwide.
Product
Pemetrexed for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0834-01
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V453000·2026-07-15
Orange EV Recalls Electric Trucks Due to Frame Rail Welding Defect
Orange EV is recalling 2020-2026 electric trucks because improper welding may cause frame rails to crack and separate, increasing the risk of loss of control.
Product
ORANGE EV — ORANGE EV E-TRIEVER, HUSK-E, T-SERIES ELECTRIC TRUCK
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-1144-2026·2026-07-15
Trafa Pharmaceuticals Organic Moringa Leaf Powder Recall
Trafa Pharmaceuticals Inc. is recalling Organic Moringa Leaf Powder due to potential Salmonella contamination. Affected product is Batch #TRF-2025050801, distributed in New York.
Product
Trafa Pharmaceuticals Inc. brand ORGANIC MORINGA LEAF POWDER; NET WEIGHT: 15 KGS; packaged in brown paper bags with a white label
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2710-2026·2026-07-15
Fletcher CT/MR Shielded Applicator Set for Gynecological Brachytherapy Recalled
Elekta's Fletcher CT/MR Shielded Applicator Set is recalled due to risk that the tip of the intrauterine tube may detach and remain inside a patient during gynecological brachytherapy treatment.
Product
Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator Product Description: The Fletcher CT/MR Shielded Applicator Set is intended for gynecological brachytherapy treatment of the cervix and endometrium.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0674-2026·2026-07-15
Azacitidine for Injection Recalled for Lack of Sterility Assurance
Reliance Life Sciences is recalling Azacitidine for Injection 100mg/Vial nationwide due to lack of sterility assurance. Patients using affected lots should contact their healthcare provider.
Product
Azacitidine for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For Subcutaneous and Intravenous Use, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0857-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-1148-2026·2026-07-15
Fresh to You Burger Chicken Fillet Deluxe with Bacon Recalled
Fresh to You Burger Chicken Fillet Deluxe with Bacon (SKU 10303) is being recalled because raw breaded chicken patties were inadvertently used instead of cooked patties, posing a risk of Salmonella contamination.
Product
Fresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10303, Net wt. 5.9oz. Product is refrigerated. UPC 1 00000 01030 3. Manufactured by LPK1 Renton, WA. Product was not sold at retail stores and sold only to employees at certain business' breakroom.
Category
Food
Distribution
2 states
SevereFDA (Drugs)·D-0673-2026·2026-07-15
Bortezomib for Injection Recalled Due to Lack of Sterility Assurance
Bortezomib for Injection 3.5mg/Vial manufactured by Reliance Life Sciences is being recalled nationwide due to lack of sterility assurance. Affected lots include RBIH0125A, RBIH0225A, RBIH0325A, and RBIH0525A distributed across the USA.
Product
Bortezomib for Injection 3.5mg/Vial, 10 mL per Single-Dose Vial, For Intravenous or Subcutaneous Use, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873. NDC: 70069-0836-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2716-2026·2026-07-15
TMINI Tracking Array knob loosening causing potential array misalignment
Think Surgical is recalling TMINI Femur and Tibia Tracking Arrays used in knee replacement surgery because the knob on the tracking array may loosen, causing potential misalignment of the array.
Product
TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V454000·2026-07-15
E-One Recalls Emergency Vehicles Due to Drive Mode Transfer Case Defect
E-One is recalling 2025-2026 Cyclone N, Typhoon N, and Commercial emergency vehicles because the drive/pump mode transfer case may disengage, causing loss of rear-wheel power.
Product
E-ONE — E-ONE COMMERCIAL, TYPHOON N, CYCLONE N
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-1140-2026·2026-07-15
EC Hot Links Seasoning 45.05# Recalled for Undeclared Sesame
Adams Extract & Spice LLC is recalling EC Hot Links Seasoning 45.05# due to undeclared sesame allergen. The product may pose a serious health risk to consumers with sesame allergies.
Product
EC Hot Links Seasoning 45.05#
Category
Food
Distribution
1 state
SevereFDA (Food)·H-1149-2026·2026-07-15
Fresh to You Burger Chicken Fillet Recall for Salmonella Risk
Fresh to You Burger Chicken Fillet sandwiches are being recalled because raw breaded chicken patties were inadvertently used instead of cooked ones, creating a risk of Salmonella foodborne illness.
Product
Fresh to You Burger Chicken Fillet, SKU 10150, Net wt. 5oz. Product is refrigerated. UPC 1 00000 01015 0. Manufactured By LPK1 Renton, WA. Product was not sold at retail stores and sold only to employees at certain business' breakroom.
Category
Food
Distribution
2 states
SevereNHTSA·26V451000·2026-07-14
Ford Explorer and Lincoln Aviator vehicles recalled for seat unlatching risk
Ford Motor Company is recalling certain 2020-2027 Aviator and 2020-2026 Explorer vehicles because the second-row seat switch may cause seats to move unexpectedly.
Product
LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26E046000·2026-07-14
Ford Recalls Integrated Trailer Brake Control Kits for F-150s
Ford is recalling specific integrated trailer module accessory kits for 2021-2026 F-150s because they may lose communication, causing a loss of trailer brakes and lights.
Product
ELECTRICAL SYSTEM: INTEGRATED TRAILER BRAKE CONTROL recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V446000·2026-07-10
Grand Design Lineage RVs Recalled for Rooftop Fan Fire Risk
Grand Design is recalling 2026-2027 Lineage RVs because a rooftop fan component may overheat and cause a fire. Dealers will replace the part free of charge.
Product
GRAND DESIGN — GRAND DESIGN LINEAGE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26E045000·2026-07-10
Tenneco Recalls NAPA Steering Inner Tie Rod Ends for Ford Vehicles
Tenneco Automotive is recalling NAPA steering inner tie rod ends for certain Ford C-Max, Escape, and Focus models because the stud may separate, causing a loss of steering.
Product
STEERING:LINKAGES:TIE ROD ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V444000·2026-07-09
2026 Volvo VNL, VNR, VHD, VN, VAH trucks recalled for loose steering
Volvo Trucks is recalling certain 2026 VNL, VNR, VHD, VN, and VAH vehicles because the steering arm may not be tightly fastened to the steering knuckle, risking loss of steering control and crashes.
Product
VOLVO — VOLVO VNL (4), VNR (4), VN, VHD
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·26610·2026-07-09
Flaunt MagSafe Battery Chargers Recalled for Fire and Burn Hazards
About 1,400 Flaunt MagSafe Battery Chargers (model E33A) are being recalled because the lithium-ion battery can overheat and ignite. The company has received five reports of the power banks catching fire, including two reports of burns and four reports of property damage.
Product
Flaunt MagSafe Battery Chargers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26608·2026-07-09
Moodooy Adult Portable Bed Rails Recalled for Entrapment and Asphyxiation Risk
Moodooy Adult Portable Bed Rails sold on Amazon violate mandatory safety standards and pose risk of entrapment and asphyxiation. The rails lack required warning labels and users can become trapped within the rail or between the rail and mattress.
Product
Moodooy Adult Portable Bed Rails
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2604-2026·2026-07-08
Omnipod DASH Pod insulin pump affected by external cannula damage
Insulet Corporation is recalling Omnipod DASH Pods worldwide due to external soft cannula damage during manufacturing that can cause insulin to leak around the pod instead of being delivered. This may lead to high blood glucose levels and, in severe cases, diabetic ketoacidosis or death.
Product
Omnipod DASH Pod. Includes the below Model/REF Numbers: 1. POD-BLE-I1-525 (5-Pack), POD-BLE-I1-520 (Single Pod). 2. POD-BLE-I1-529 (10-Pack), POD-BLE-I1-520 (Single Pod). 3. BLE-I1-529 (10-Pack), BLE-I1-520 (Single Pod). 4. BLE-C1-529 (10-Pack), BLE-C1-520 (Single
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2672-2026·2026-07-08
GORE TAG Thoracic Branch Endoprosthesis Side Branch Component Recall
W. L. Gore & Associates is recalling 467 GORE TAG Thoracic Branch Endoprosthesis Side Branch Components worldwide due to risk of catheter separation during deployment.
Product
GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes Puerto Rico) and Canada: TSB080806A, TSB081006A, TSB081206A, TSB081506A, TSB081706A, TSB121506A, TSB121706A, TSB122006A EMEA Countries, Australia, New Zealand:
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2644-2026·2026-07-08
Cyberknife Treatment Delivery System Collimator Docking and Fall Hazard Recall
Accuray Incorporated is recalling Cyberknife Treatment Delivery Systems with the Xchange Robotic Collimator Changer because a collimator may fail to fully dock and fall from the housing if room-control pendant motion is initiated while the system interlock is bypassed.
Product
Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer; Linear Accelerator
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0653-2026·2026-07-08
IMULDOSA injection recalled due to lack of sterility assurance
Accord BioPharma is recalling IMULDOSA (ustekinumab-srlf) Injection due to lack of assurance of sterility. The affected lot was distributed nationwide.
Product
IMULDOSA — IMULDOSA (USTEKINUMAB-SRLF)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2605-2026·2026-07-08
Omnipod Eros Pod Insulin Delivery Failure Risk
Insulet Corporation is recalling Omnipod (Eros) Pod units due to external soft cannula damage during manufacturing that can cause insulin leakage instead of delivery to the user. High blood glucose levels and serious complications including diabetic ketoacidosis (DKA) or death may result from under-delivery of insulin.
Product
Omnipod (Eros) Pod. Includes the below Model/REF Numbers: 1. POD-ZXP425 (10 Pack), POD- ZXP420 (Single Pod). 2. ZXR425 (10-Pack), ZXR420 (Single Pod). 3. ZXP425 (10 Pack), ZXP420 (Single Pod).
Category
Medical Device
Distribution
Distributed nationwide

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351–375 of 36488