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

5901–5925 of 90258

HighFDA (Devices)·Z-2597-2025·2025-10-01
Big Bore CT systems recalled because patient table may descend unexpectedly
Philips Big Bore RT, Brilliance CT Big Bore Oncology and Brilliance CT Big Bore systems are recalled because the patient support table may descend unexpectedly after a ball screw replacement. 33 units are affected.
Product
Philips CT systems labeled as the following: 1. Big Bore RT, Model Number: 728242. 2. Brilliance CT Big Bore Oncology, Model Number: 728243. 3. Brilliance CT Big Bore, Model Number: 728244.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0663-2025·2025-10-01
Artisan of Skin acne treatment recalled over elevated benzene levels
Artisan of Skin Benzoyl Peroxide 10%, 7 oz, lots 58170A and 58172A, is recalled because of elevated levels of benzene. 125 units distributed in California and Georgia are affected.
Product
ARTISAN OF SKIN (Benzoyl Peroxide 10%) , 7 oz (201 g), Artisan of Skin Beverly Hills, CA 90210
Category
Drug
Distribution
2 states
HighFDA (Devices)·Z-2629-2025·2025-10-01
Allura Xper FD20 Biplane OR Table recalled over internal component deterioration
Philips Allura Xper FD20 Biplane OR Table systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 5 units are affected.
Product
Allura Xper FD20 Biplane OR Table Product Codes: (1)722020, (2) 722025; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0621-2025·2025-10-01
CBD and THC gummies recalled over potential peanut protein cross-contact
Extract Labs Sugar-free Mixed Berry Gummies, lot 25E5082907A, are recalled because of potential peanut protein cross-contact. 2,180 gummies in 109 bottles are affected.
Product
Sugar-free Mixed Berry Gummies Brand Name: Extract Labs Generic Name: Dietary Supplement Strength: 10mg CBD and 10mg D9 THC per gummy Dosage: 1 gummy Form: Gummy Administration: Oral Intended use: Dietary Supplement Type of packaging: 225cc amber packer bottle with…
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-2604-2025·2025-10-01
CT 6000 scanners recalled because the patient table may drop unexpectedly
Philips CT 6000 systems, model 728307, are recalled because the patient support table may descend unexpectedly due to ball screw misalignment after a replacement. 6 units are affected.
Product
Philips CT systems labeled as the following: 1. CT 6000, Model Number: 728307.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2598-2025·2025-10-01
Brilliance iCT systems recalled over ball screw misalignment dropping the couch
Philips Brilliance iCT systems, model 728306, are recalled because the patient support table may descend unexpectedly after a ball screw replacement. 210 units are affected.
Product
Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2636-2025·2025-10-01
Vessel harvesting systems recalled after out-of-box failures in harvesting tool jaws
Vasoview Hemopro 3 Endoscopic Vessel Harvesting Systems are recalled after out-of-box failures including deformed jaw attachments, jaws not fully closed and lifted heater wire. 98 units are affected.
Product
Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW HEMOPRO 3 Endoscopic Vessel Harvesting (EVH) System (VH-6000, VH-6001, and VH-6010) is a vessel harvesting kit designed for use with a 7 mm endoscope to cut and cauterize vessel branches.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2595-2025·2025-10-01
Brilliance CT 40 and 64 channel systems recalled over unexpected couch descent
Philips Brilliance CT 40 Channel, Brilliance CT 64 Channel and Ingenuity Flex systems are recalled because the patient support table may descend unexpectedly after a ball screw replacement. 181 units are affected.
Product
Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel, Model Number: 728235. 2. Brilliance CT 64 Channel, Model Number: 728231. 3. Ingenuity Flex, Model Number: 728317
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2635-2025·2025-10-01
Allura CV20 systems recalled over internal component deterioration disabling motorized movement
Philips Allura CV20 systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 46 units are affected.
Product
Allura CV20; Product Code: 722031; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2634-2025·2025-10-01
Allura Xper FD20/15 OR Table recalled over internal component deterioration
The Philips Allura Xper FD20/15 OR Table is recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. One unit is affected.
Product
Allura Xper FD20/15 OR Table; Product Code: 722059; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2628-2025·2025-10-01
Allura Xper FD20 OR Table recalled over CMOS battery and drive deterioration
Philips Allura Xper FD20 OR Table systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 174 units are affected.
Product
Allura Xper FD20 OR Table Product Codes: (1)722023, (2) 722035, (3) 722015; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2622-2025·2025-10-01
Patient monitors recalled over potential activation of an abnormal alarm pause
BeneVision N1 Patient Monitors are recalled because of the potential for activation of an abnormal alarm pause. 2,278 units are affected.
Product
BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017, 6660E-PA00014, 6660E-PA00012, 6660E-PA00011, 6660E-PA00018, 6660E-PA00015, 6660E-PA00020, Q6660E-PA00011, 6660E-PA00021, 6660E-PA00016, 6660E-PA00019, Q6660E-PA00018, 6660E-PA00010, Q6660E-PA00010, Q6660E-PA00021…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2625-2025·2025-10-01
Allura Xper FD10 OR Table recalled over ageing power supply and drive
Philips Allura Xper FD10 OR Table systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 2 units are affected.
Product
Allura Xper FD10 OR Table Product Codes: (1)722022, (2) 722033; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V653000·2025-09-30
Thor motorhome propane tank support weld can fracture releasing the tank
Thor Motor Coach is recalling certain 2024-2025 Luminate and Indigo RVs because the LP tank support tube may be too short with an insufficient weld that can fracture, allowing the tank to detach.
Product
THOR MOTOR COACH — THOR MOTOR COACH INDIGO, LUMINATE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V654000·2025-09-30
Volvo EX90 power tailgate can suddenly drop from detached spindle nut
Volvo is recalling certain 2025 EX90 vehicles because a spindle nut may detach from the power operated tailgate drive units, causing the tailgate to drop suddenly. Owners are told not to use the feature.
Product
VOLVO — VOLVO EX90
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25E063000·2025-09-30
Q'Straint Recalls QRT-Deluxe and QRT-Max Wheelchair Restraints
Q'Straint is recalling QRT-Deluxe and QRT-Max wheelchair restraints because the retractors may not lock, preventing the wheelchair from being properly secured.
Product
EQUIPMENT ADAPTIVE/MOBILITY:WHEELCHAIR RESTRAINTS/SECUREMENT:LATCH/ANCHOR: recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·25V655000·2025-09-30
2021-2022 Nissan Leaf recalled for battery overheating during Level 3 fast charging
Nissan is recalling certain 2021-2022 Leaf vehicles with Level 3 quick charging capability because the lithium-ion battery may overheat during fast charging, increasing fire risk. Owners should not use Level 3 charging until a free software update becomes available.
Product
NISSAN — NISSAN LEAF
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·030-2025·2025-09-27
Hillshire Brands Recalls Corn Dogs and Sausage Sticks Due to Wood Contamination
Hillshire Brands is recalling corn dog and sausage on a stick products nationwide due to possible wood contamination. Consumers should discard or return the affected items.
Product
The Hillshire Brands Company — The Hillshire Brands Company Recalls Corn Dog and Sausage On A Stick Products Due To Possible Extraneous Matter Contamination
Category
Food
Distribution
Distributed nationwide
HighNHTSA·25E062000·2025-09-26
Medix Recalls Phoenix Quick Liner Wheel Covers on Ford Ambulances
Medix Specialty Vehicles is recalling Phoenix Quick Liner Wheel Covers on Ford Type-III ambulances because they may detach during transit, creating a road hazard.
Product
WHEELS:HUBCAP/COVER recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V642000·2025-09-25
Jeep Wagoneer quarter window trim may not be properly secured
Chrysler is recalling certain 2022-2024 Jeep Wagoneer and Grand Wagoneer vehicles because the quarter trim on the driver and passenger windows may not have been properly secured and can detach.
Product
JEEP — JEEP WAGONEER, GRAND WAGONEER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25E061000·2025-09-25
Cognito Motorsports Recalls Rev C Ball Joints for GMC and Chevrolet Trucks
Cognito Motorsports is recalling 12,160 Rev C Ball Joints installed on 2011-2025 GMC and Chevrolet 2500HD and 3500HD trucks because the ball stud may pull through the housing, risking loss of steering.
Product
SUSPENSION:FRONT:CONTROL ARM:UPPER BALL JOINT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V646000·2025-09-25
School bus tire can damage air line activating the parking brake
International is recalling certain 2024-2026 IC Bus CESB school buses because a tire may contact and damage the air dryer discharge line, causing an air leak that unintentionally applies the parking brake.
Product
IC BUS — IC BUS CESB
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·25475·2025-09-25
Countertop ovens recalled after 95 reports of doors closing and burning users
About 1,290,000 Oster French Door Countertop Ovens are recalled because the doors can unexpectedly close. Sunbeam has 95 reports of doors closing and causing burns, including two second-degree burns.
Product
Oster French Door Countertop Ovens
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25476·2025-09-25
Cooling gel seat pads recalled after a child suffered second degree burns
About 20,000 Hoovy Cooling Gel Insert Pads for car seats and strollers are recalled because they can become hot in the sun or a hot car. One child suffered second degree burns requiring medical attention.
Product
Hoovy Cooling Gel Insert Pads for Car Seats and Strollers
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·25V643000·2025-09-25
BMW Recalls 2026 M4 and 430i Vehicles for Fire Risk
BMW is recalling 2026 M4 and 430i vehicles because improperly connected battery cables may cause engine stalls or fires.
Product
BMW — BMW 430I, M4
Category
Vehicle
Distribution
Distributed nationwide

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