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

8501–8525 of 31218

ModerateFDA (Devices)·Z-1274-2025·2025-03-12
Hiossen Dental Abutments Misidentified on Patient Chart Stickers
Hiossen is recalling patient chart stickers for dental abutments that incorrectly identify product versions. Stickers mislabel ET Rigid Abutments as Regular and ET Multi Abutments as Mini. Dentists should verify actual product versions against packaging labels.
Product
Osstem Implant System - Abutment ET Multi Abutment Size: 4.8D 3.0G/H- Abutment is intended for use with a dental implant to provide suport for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETMTA503RV1
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1273-2025·2025-03-12
Dental Abutments Recalled for Incorrect Version Identification Stickers
Hiossen Inc. is recalling ET Rigid Abutments due to incorrect patient chart stickers that misidentify product versions. The stickers may label Mini abutments as Regular or identify other abutment models incorrectly, risking use of the wrong component.
Product
ET Rigid Abutment (Mini) SIze: 4.5D 4.0G/H 4.0H - Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETRGA4544MP
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0643-2025·2025-03-12
Orgeat Almond Syrup Recalled Due to Potential Yeast Contamination
A C Calderoni & Co. Inc. is recalling Orgeat Almond Syrup due to potential yeast contamination in the product. The affected product was distributed to foodservice distributors and restaurants in California.
Product
ORGEAT ALMOND SYRUP; 32 fl oz (946 ml); Glass bottle with screw-top lid; Contains: Sugar, Water, Citric Acid Natural Flavor, Sodium Benzoate; Refrigerate after opening
Category
Food
Distribution
0 states
ModerateFDA (Drugs)·D-0250-2025·2025-03-12
Vitamin D Supplement Oral Syringes Recalled for Defective Delivery System
Safecor Health is recalling 3069 units of Ergocalciferol (Vitamin D Supplement) oral syringes nationwide due to leakage in the repackaged unit-dose delivery system. No illnesses have been reported.
Product
Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) per 0.05 mL Oral Syringe, Delivers: 0.05 mL Oral Solution, Mfg by: Westminster, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: 69367028302.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1296-2025·2025-03-12
BD BBL TB Stain Kit Expiration Date Labeling Discrepancy
BD BBL TB Stain Kit component shipped with incorrect expiration date labeling. One component has printed expiration 30 September 2024 while Certificate of Analysis indicates 30 April 2025, creating confusion about product validity.
Product
BD BBL TB Stain Kit K, Catalog (REF): 212522
Category
Medical Device
Distribution
14 states
ModerateFDA (Drugs)·D-0251-2025·2025-03-12
Simethicone Oral Syringe Recalled for Defective Delivery System
Safecor Health is recalling Simethicone 20 mg oral syringes due to leakage caused by a defective delivery system. Approximately 10,992 syringes were distributed nationwide.
Product
Simethicone 20 mg per 0.3 mL Oral Syringe, Delivers: 0.3 mL, Oral Drops, Mfg By: Rugby, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: 00536130375.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1272-2025·2025-03-12
Dental abutment implants recalled for incorrect patient chart stickers
Hiossen Inc. is recalling ET Rigid Abutment (Mini) dental implant components due to patient chart stickers that incorrectly identify the product version. The stickers may identify Mini versions as Regular, or Multi-versions as Mini.
Product
ET Rigid Abutment (Mini) SIze: 4.5D 3.0G/H 7.0H - Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETRGA4537MP
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1292-2025·2025-03-12
Vios bedside monitor batteries may deplete during storage
Murata Vios bedside monitors may experience battery depletion if stored without power, causing tablet connectivity issues. Affected units should be kept plugged in while in storage.
Product
Vios Monitoring System Bedside Monitor Model BSM2050
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1251-2025·2025-03-12
Infiltration Cannula Recalled Due to Incorrect Water Jet Pattern
HUMAN MED AG is recalling 775 Biofill Infiltration Cannulas because the water jet may emerge as a spot jet rather than the specified fan-shaped spray pattern, affecting device functionality.
Product
human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107, sterile, single use.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1290-2025·2025-03-12
Lumenis Pulse 120H Laser System Charger May Prevent Device Startup
Lumenis recalled three Pulse 120H laser systems due to a charger defect. The charger's initial current can damage AC controller power resistors, preventing the device from powering on.
Product
(1) Lumenis Pulse 120H 30 amp, REF GA 2009996, Laser System; (2) Lumenis Pulse 120H, Moses 2.0 (DOM), REF GA0006802, Laser System; and (3) Lumenis Pulse 120H, REF GA-0008700, Laser System.
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-1271-2025·2025-03-12
Dental implant abutments recalled for incorrect packaging labels
Hiossen has recalled ET Rigid Abutment dental implant components because stickers in the packaging mislabel whether products are Mini or Regular versions. Incorrect identification could affect proper implant installation.
Product
ET Rigid Abutment (Mini) Size 4.5D 1.0G/H 5.0H - Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. GA4515MP Model/Catalog Number: ETRGA4515MP
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1252-2025·2025-03-12
Philips IntelliSpace Cardiovascular Software Data Archival Failure Recall
Philips cardiovascular diagnostic software version 7.0.0.0 cannot archive, copy, or export study data, affecting 139 units distributed nationwide. Users may experience data management and workflow disruptions.
Product
Philips IntelliSpace Cardiovascular software, Model 830089.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0603-2025·2025-03-12
Noble Made Garlic Parmesan Wing Sauce recalled for foaming issue
Noble Made Garlic Parmesan Wing Sauce is being recalled due to customer complaints of bottles foaming when opened. The product was distributed to retail locations across multiple states.
Product
Noble Made Garlic Parmesan Wing Sauce, net wt 9.25oz, UPC 850000398542, #0897 BEST BY 06/02/2026 14:02 33724 L1, Code: F20920061
Category
Food
Distribution
18 states
ModerateFDA (Devices)·Z-1275-2025·2025-03-12
ET Rigid and Multi Dental Abutments Recalled for Incorrect Identification Stickers
Hiossen recalled ET Rigid and Multi dental abutments for incorrect identification stickers in packaging that misidentify product versions, risking improper placement during installation.
Product
ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETRGA4524MP
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V865000·2025-03-11
Fisker Ocean 2023-2024 Transmission Defect May Cause Vehicle Rollaway
Certain 2023-2024 Fisker Ocean vehicles have a transmission software defect that may prevent gear engagement, allowing the vehicle to roll away while in Drive or Reverse. A free software update was released March 11, 2024.
Product
FISKER — 2024 FISKER OCEAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V863000·2025-03-11
2025 Grand Design Lineage motorhomes recalled for faulty battery warming pad
2025 Lineage motorhomes may have incorrectly installed battery warming pads that can damage wiring and cause electrical shorts with fire risk. Grand Design will replace the pads free of charge.
Product
GRAND DESIGN — 2025 GRAND DESIGN LINEAGE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V753000·2025-03-11
Volvo VAH trucks recalled for seat belt anchor defects
Volvo Trucks is recalling 2019-2026 VAH trucks because the passenger seat belt anchor may fail due to inadequate floor reinforcement, preventing proper occupant restraint in crashes.
Product
VOLVO — 2019 VOLVO VAH
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V757000·2025-03-11
2026 Volvo VNL trucks recalled for roof center marker light failure
Volvo Trucks is recalling certain 2026 VNL commercial trucks because the roof center marker lights may fail to illuminate, reducing visibility and increasing crash risk.
Product
VOLVO — 2026 VOLVO VNL (4)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V861000·2025-03-11
Grand Design 2022 Travel Trailers Recalled for LP Gas System Leak
Grand Design is recalling 30,435 units of 2022 travel trailers due to cracked LP gas system fittings that may cause leaks and fire risk. Dealers will replace affected parts free of charge.
Product
GRAND DESIGN — 2022 GRAND DESIGN TRANSCEND
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V767000·2025-03-10
2024 Toyota Sequoia Hybrid and Tundra Tire Sidewall Damage Recall
Certain 2024 Toyota Sequoia Hybrid, Tundra, and Tundra Hybrid vehicles are recalled due to passenger-side front and rear tire sidewall damage that may cause sudden tire pressure loss and loss of vehicle control.
Product
TOYOTA — 2024 TOYOTA SEQUOIA HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V727000·2025-03-10
Ford Mustang Brake Fluid Warning System Software Recall
Ford is recalling 2020-2023 Mustang vehicles because the brake fluid level sensor may fail to illuminate the warning light when brake fluid is low. Drivers could operate the vehicle with insufficient brake fluid, reducing braking performance and increasing crash risk.
Product
FORD — 2021 FORD MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V664000·2025-03-10
Recreational vehicles recalled for propane hose damage and fire hazard
REV is recalling 2024-2026 Fleetwood Fortis and Holiday Rambler Invicta RVs with theater seats because theater seat fasteners may have damaged propane hoses, creating a fire hazard.
Product
FLEETWOOD — 2024 FLEETWOOD FORTIS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V764000·2025-03-10
2018–2022 BMW X3 rear cargo rail attachment defect recall
BMW is recalling 2018–2022 X3 vehicles because rear cargo rail attachment bolts may become damaged in a rear crash, causing the rail to detach and increasing injury risk. Dealers will replace the bolts free of charge.
Product
BMW — 2020 BMW X3
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V570000·2025-03-09
Ducati Motorcycles Recalled for Defective Rear Wheel Axle
Ducati is recalling certain 2018-2025 motorcycles because the rear wheel axle may lose structural integrity and break during riding, risking loss of control. Dealers will replace the axle free of charge.
Product
DUCATI — 2020 DUCATI PANIGALE V4 R
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V653000·2025-03-09
Peterbilt 567 and 579 Trucks: Fuel Tank Puncture Risk from Loose U-bolts
PACCAR is recalling 2021-2024 Peterbilt 567 and 579 trucks. U-bolts securing the air tank can contact and wear through the fuel tank over time. A punctured tank can leak fuel, increasing the risk of fire.
Product
PETERBILT — 2021 PETERBILT 567
Category
Vehicle
Distribution
Distributed nationwide

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8501–8525 of 31218