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 the agency’s own highest classification or reported deaths or serious injuries, 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

1326–1350 of 39697

SevereFDA (Food)·H-0591-2026·2026-04-01
Trader Joe's Japanese Style Fried Rice recalled for glass fragments
Ajinomoto Foods North America Inc. is recalling Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed (1 lb. bags) due to glass fragments 1–3 cm long and 2–4 mm wide found in the product.
Product
Item 5650173 Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed. SKU #097908. Net wt. 1lb. per bag. Retail bag UPC 00979085. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 24/1lb. bags per…
Category
Food
Distribution
43 states
SevereFDA (Food)·H-0647-2026·2026-04-01
SiluetaYa Mexican Tejocote Roots Supplement Pieces Recalled for Yellow Oleander
SiluetaYa Mexican Tejocote Roots Supplement Pieces (7g bottles, Lot US1220) are recalled because the product contains yellow oleander, a toxic substance. The product was distributed online to consumers in AZ, CA, NM, NY, TX, and UT.
Product
SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#: 7500464462411, Lot: US1220 " Expiration Date: 06/2027
Category
Food
Distribution
6 states
SevereFDA (Devices)·Z-1617-2026·2026-04-01
Trilogy Evo Universal ventilator recalled as Class I over tidal volume
Philips Respironics is recalling the Trilogy Evo Universal ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Product
Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0619-2026·2026-04-01
Focaccia Bread Products Recalled for Metal Fragments
Bakkavor is recalling roasted tomato and parmesan focaccia bread sold under multiple retail brands due to metal fragments discovered in the products. The metal originated from roasted tomatoes supplied by an ingredient supplier.
Product
Roasted Tomato Parmesan Focaccia Bread sold under the brand names of FREDERIK'S by meijer SLOW-ROASTED TOMATO & SHREDDED PARMESAN CHEESE NET WT 13.75 OZ (390g) UPC 7 13733 88387 0 DIST. BY MEIJER DISTRIBUTION, INC. GRAND RAPIDS, MI 49544; fresh & simple Roasted Tomato &…
Category
Food
Distribution
10 states
SevereFDA (Devices)·Z-1576-2026·2026-04-01
ProGuide chronic dialysis catheters recalled as Class I over sheath introducer defect
Merit Medical is recalling ProGuide Chronic Dialysis Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
Product
ProGuide Chronic Dialysis Catheters, REF: DC01455550/C, DC21452419/C, DC21452419-NE5/C, DC21452823-NE5/C, DC21454035/C, DC21455550/C
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0649-2026·2026-04-01
Doraditas de Azucar recalled due to missing allergen labeling
Distribuidora de Alimentos Sendero LLC is recalling Doraditas de Azucar because the product label is missing declarations for wheat and soy allergens.
Product
Doraditas de Azucar UPC 5901234123457
Category
Food
Distribution
1 state
SevereFDA (Food)·H-0630-2026·2026-04-01
Lucerne 2% Cottage Cheese recalled for metal fragments
Lucerne 2% Cottage Cheese 24 oz. tubs are being recalled due to the potential presence of metal spring fragments. Consumers who have purchased affected product should not consume it.
Product
Lucerne 2% Cottage Cheese 2% Milkfat Small Curd Vitamin A Added Grade A. Net wt.24oz. Perishable and keep refrigerated. Consumer package is a plastic cup with foil lid and clear plastic lid. UPC 0 21130 07662 8. Distributed by Lucerne Foods, Inc PO Box 99, Pleasanton, CA.…
Category
Food
Distribution
5 states
SevereFDA (Devices)·Z-1567-2026·2026-04-01
Erbe flexible cryoprobe 20402-410 recalled as Class I over rupture
Erbe USA is recalling the Flexible Cryoprobe REF 20402-410 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
Product
Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1566-2026·2026-04-01
Erbe flexible cryoprobe 20402-401 recalled as Class I over rupture
Erbe USA is recalling the Flexible Cryoprobe REF 20402-401 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
Product
Flexible Cryoprobe (OD 1.1mm, L1.15mm) w/ oversheath (OD2.6mm, L817mm) REF: 20402-401 STERILE EO. For surgical use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1615-2026·2026-04-01
Trilogy Evo O2 ventilator recalled as Class I over tidal volume
Philips Respironics is recalling the Trilogy Evo O2 ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Product
Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0632-2026·2026-04-01
Nuts.com Espresso Malted Milk Balls Recalled for Undeclared Wheat and Soy
Nuts.com is recalling Espresso Malted Milk Balls sold in 1 lb. and 20 lb. packages because the labels do not declare wheat and soy allergens that are present in the product.
Product
Nuts.com, Espresso Malted Milk Balls, 1 lb. sealed pouch & 20 lb. clear poly bag in Nuts.com cardboard box . Packages are only sold individually .
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1579-2026·2026-04-01
BioFlo DuraMax catheters recalled as Class I over sheath introducer defect
Merit Medical is recalling BioFlo DuraMax Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
Product
BioFlo DuraMax Catheter, REF: H965103028011/A, H965103028021/A, H965103028021/EU, H965103028031/A, H965103028031/EU, H965103028041/A, H965103028041/EU, H965103028051/A, H965103028051/EU, H965103028061/A, H965103028061/EU, H965103028070/A, H965103028070/EU, H965103028080/A…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V210000·2026-04-01
Isuzu and Chevrolet Commercial Trucks Recalled for Wire Harness Chafing
Isuzu is recalling 2025-2027 commercial trucks because wire harnesses may chafe, causing engine stalls, brake failures, or fires.
Product
ISUZU — ISUZU CHEVROLET LCF 4500HD, NPR HD, CHEVROLET LCF 5500XD, NPR XD
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1568-2026·2026-04-01
Erbe flexible cryoprobe 20402-411 recalled as Class I over rupture
Erbe USA is recalling the Flexible Cryoprobe REF 20402-411 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
Product
Flexible Cryoprobe (OD 2.4mm, L1.15mm) REF: 20402-411. For surgical use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1588-2026·2026-04-01
Heating pad recalled as Class I because folding causes excessive temperatures
Navajo Manufacturing is recalling the Handy Solutions Neck & Shoulders Heating Pad because folding it during use raises power density in the folded area, causing excessive temperatures the limit device cannot sense.
Product
Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V201000·2026-03-31
2025–2026 Ford Bronco Sport and Maverick Occupant Sensor Recall
Ford is recalling certain 2025–2026 Bronco Sport and Maverick vehicles because the front passenger occupant classification sensor may fail to detect a passenger, risking failure of the airbag to deploy in a crash.
Product
FORD — FORD MAVERICK, BRONCO SPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V205000·2026-03-31
2026 Ford Explorer and Mustang Engine Piston Circlip Defect Recall
Ford is recalling certain 2026 Explorer and Mustang vehicles because engine piston circlips may have been incorrectly installed, risking loss of drive power and increasing crash risk.
Product
FORD — FORD EXPLORER, MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V200000·2026-03-29
Aston Martin DBX rear lower suspension arm may crack or shear
Aston Martin is recalling certain 2021-2026 DBX, DBX707 and DBX S vehicles because the torque reaction link pin may slide out of the rear lower suspension arm, cracking or shearing the arm casting.
Product
ASTON MARTIN — ASTON MARTIN DBX, DBX S, DBX707
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V198000·2026-03-27
Mercedes-Benz Recalls 2025 G 580 EV Due to Incorrect Wheel Bolts
Mercedes-Benz is recalling 2025 G 580 EVs because incorrect wheel bolts may have been installed, posing a risk of wheel detachment and crashes.
Product
MERCEDES-BENZ — MERCEDES-BENZ G 580 EV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V196000·2026-03-27
KTM 390 electronic throttle control may fail after water entry
KTM is recalling certain 2022-2023 390 Duke and 2022-2024 RC 390 motorcycles because water may enter the electronic throttle control unit and cause it to fail, losing drive power while riding.
Product
KTM — KTM RC 390, 390 DUKE
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·26341·2026-03-26
Vive Health bed rails recalled after two reported entrapment deaths
Vive Health is recalling three bed rail models after two reported entrapment deaths. Users can become entrapped within the rail or between the rail and the mattress.
Product
Vive Health Bed Rails
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26348·2026-03-26
FUNTOK ride-on truck circuit boards can overheat and ignite
FUNTOK 24V 2-Seater Ride-On Trucks are being recalled because the circuit board can overheat and ignite. Eleven reports of fires, sparking, burning, melting and smoking have been received.
Product
FUNTOK 24V 2-Seater Ride-On Trucks
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26339·2026-03-26
Nexgrill wire bristle grill brushes can shed bristles onto food
Nexgrill is recalling metal wire bristle grill brushes because bristles can detach and stick to the grill or food. Five consumers swallowed bristles and sought medical treatment.
Product
Metal Wire Bristle Grill Brushes
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·26V192000·2026-03-26
Lucid Recalls 2025-2026 Gravity Vehicles Due to Seat Belt Anchor Defect
Lucid is recalling 2025-2026 Gravity vehicles because second-row seat belt anchor brackets may have insufficient welds, increasing injury risk in a crash.
Product
LUCID — LUCID GRAVITY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26E014000·2026-03-26
Chrysler Recalls Mopar Side Curtain Air Bags for Seam Defect
Chrysler is recalling specific Mopar side curtain air bags because improperly sealed seams may cause insufficient pressure retention, increasing the risk of ejection and injury during a crash.
Product
AIR BAGS:SIDE/WINDOW:CURTAIN recall
Category
Vehicle
Distribution
Distributed nationwide

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1326–1350 of 39697