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

3301–3325 of 6105

CriticalFDA (Devices)·Z-1650-2023·2023-06-14
Philips Trilogy and LifeVent ventilator models recalled for flow sensor debris
Environmental debris accumulation may block flow sensors in Philips ventilators, potentially preventing accurate pressure and flow delivery to patients.
Product
Trilogy Evo O2 and LifeVent EVO2, Model Numbers DS2100X11B, IN2100X15B, IN2100X19, FX2100X15B, LA2100X15B, IA2100X15B, FP2100X10, FR2100X14B, ND2100X15B, IT2100X21B, ES2100X15B, DE2100X13B, EU2100X15B, EU2100X19, EE2100X15B, and SP2100X26B
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0976-2023·2023-06-14
Tastykake Chocolate Kandy Kakes recalled for undeclared peanuts
Tastykake Chocolate Kandy Kakes are being recalled due to undeclared peanuts. The product poses a serious risk to individuals with peanut allergies.
Product
Tastykake Chocolate Kandy Kakes NET WT 8 OZ (227g) 6-1.3 OZ (38g) PKGS TASTY BAKING COMPANY, PHILADELPHIA, PA 19112 UPC 0 25600 00225 4
Category
Food
Distribution
6 states
CriticalFDA (Food)·F-0983-2023·2023-06-14
Cookies Recalled for Undeclared Soy and Wheat Allergens
TETAS Mireya, SABOR Galleta Oreo cookies are being recalled due to undeclared soy and wheat allergens. Consumers with soy or wheat allergies should not consume this product.
Product
TETAS Mireya, SABOR Galleta Oreo
Category
Food
Distribution
0 states
CriticalFDA (Devices)·Z-1666-2023·2023-06-14
StealthStation Cranial Software displays inaccurate navigation during brain surgery
A software anomaly in Medtronic's StealthStation Cranial Software may cause inaccurate surgical navigation during brain procedures. This can result in unintended tissue damage and prolonged surgery.
Product
StealthStation Cranial Software, Model: 9735585, used with StealthStation S7/i7 systems
Category
Medical Device
Distribution
1 state
SevereFDA (Food)·F-0980-2023·2023-06-14
TETAS Mireya candy recalled for undeclared soy and walnut allergens
DIBE LLC is recalling TETAS Mireya candy due to undeclared soy and walnut allergens. Consumers with allergies to these ingredients should not consume the product.
Product
TETAS Mireya, SABOR Ferrero
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1649-2023·2023-06-14
Philips Respironics Ventilators Recalled for Flow Sensor Debris Accumulation
Philips Respironics recalled approximately 57,395 ventilators due to environmental debris potentially accumulating on the flow sensor, which may prevent accurate delivery of pressure and volume to patients, risking hypoxemia.
Product
Trilogy Evo, Garbin Evo, and Aeris EVO, Model Numbers DS2110X11B, IN2110X15B, JP2110X16B, AU2110X15B, LA2110X15B, CA2110X12B, BR2110X18B, KR2110X15B, IA2110X15B, FP2110X10, FR2110X14B, ND2110X15B, IT2110X21B, ES2110X15B, DE2110X13B, BL2110X15B, GB2110X15B, EU2110X15B, EE2110X15B,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0974-2023·2023-06-14
Dark Chocolate Almonds Recalled Due to Undeclared Milk Allergen
Meijer Inc is recalling Frederik's by Meijer Dark Chocolate Almonds due to undeclared milk. The product was distributed to Meijer stores in six Midwest states.
Product
Frederik's by Meijer Dark Chocolate Almonds, 12oz stand-up pouch, UPC 7-08820-68730-1
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0979-2023·2023-06-14
TETAS Mireya Galleta Maria Cookies Recalled for Undeclared Soy and Wheat
DIBE LLC is recalling TETAS Mireya SABOR Galleta Maria cookies due to undeclared soy and wheat allergens. Consumers with allergies to these ingredients should not consume the product.
Product
TETAS Mireya, SABOR Galleta Maria
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1630-2023·2023-06-14
StealthStation Cranial Software Depth Gauge Synchronization Failure Risk
A software anomaly in StealthStation Cranial Software causes depth gauge displays to lose synchronization during cranial biopsy procedures, risking inaccurate surgical guidance and tissue injury.
Product
StealthStation Cranial Software, Models: 9735585, 9735586 (kit), 9735587 (kit), used with StealthStation S7/i7 systems
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0977-2023·2023-06-14
Onion Powder Premium Recalled for Potential Salmonella Contamination
Olam Food Ingredients is recalling Onion Powder Premium sold in bulk fiber bags due to potential Salmonella contamination. Affected product was distributed to Canada, Arkansas, and Illinois.
Product
Onion Powder Premium, 44.9 and 50 lb. fiber bags sold as bulk ingredient
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1633-2023·2023-06-14
FDA Recalls Walnut Wearable Smart Thermometer Due to Reported Skin Burns
BearCare's Walnut Wearable Smart Thermometer (Model WT20) is being recalled due to reports of skin burns in children ages 0-6. The device was distributed nationwide; 1818 units were affected.
Product
Walnut Wearable Smart Thermometer, intended for continuous chest temperature monitoring of children ages 0-6 years in non-emergency medical situations, Model Number WT20
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1651-2023·2023-06-14
Trilogy Evo O2 EV300 respiratory devices recalled for debris accumulation
Philips Respironics recalled 18,855 Trilogy Evo O2 EV300 devices because environmental debris may accumulate on the flow sensor, potentially causing inaccurate delivery of pressure or flow. This could result in patient hypoxemia if not promptly addressed.
Product
Trilogy Evo O2 EV300, Model Numbers DS2200X11B, IN2200X15B, FX2200X15B, CA2200X12B, FR2200X14B, ND2200X15B, ES2200X15B, BL2200X15B, GB2200X15B, EU2200X15B, EE2200X15B, and TR2200X15B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0975-2023·2023-06-14
Food Recall: Meijer Express Dark Chocolate Covered Almonds Due to Undeclared Milk
Meijer Inc is recalling Meijer Express Dark Chocolate Covered Almonds due to undeclared milk, a serious risk for consumers with milk allergies. The recall affects 9,030 units in Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.
Product
Meijer Express Dark Chocolate Covered Almonds, 7.5oz plastic cup with lid, UPC 7-60236-19787-4
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1652-2023·2023-06-14
Trilogy Evo Universal Ventilator Class I Recall—22,237 Units Affected
The FDA has issued a Class I recall for the Trilogy Evo Universal Ventilator Model DS2000X11B, affecting 22,237 units distributed nationwide and globally. The device is manufactured by Philips Respironics, Inc.
Product
Trilogy Evo Universal Ventilator, Model Number DS2000X11B
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·23V421000·2023-06-12
2022 Nissan Sentra: Driver Cowl Seal Defect May Cause Electrical Failures
The 2022 Nissan Sentra may have a defective driver's side cowl seal, allowing water intrusion and electrical corrosion. This could cause loss of airbag function, exterior lighting, and braking safety features, increasing crash and fire risk.
Product
NISSAN — 2022 NISSAN SENTRA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V413000·2023-06-08
Jeep Grand Cherokee Models Recalled for Detaching Rear Coil Springs
Chrysler is recalling certain 2022-2023 Jeep Grand Cherokee and 2021-2023 Jeep Grand Cherokee L vehicles. Rear coil springs may detach while driving, creating a crash risk; dealers will repair them free.
Product
JEEP — 2021 JEEP GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0957-2023·2023-06-07
Living Nutz Nut & Seed Butter Recalled for Potential Salmonella Contamination
Living Nutz Nut & Seed Butter products have been recalled due to potential Salmonella contamination. The recall affects 68 units distributed across seven states.
Product
Living Nutz Nut & Seed Butter Raw Sprouted & Stoneground; 8 oz., 12 oz. or 64 oz.
Category
Food
Distribution
7 states
SevereFDA (Food)·F-0966-2023·2023-06-07
Black Fungus Golden Koi Recalled for Possible Salmonella Contamination
AH USA Group Inc is recalling Black Fungus Golden Koi 2.5 oz packages due to potential salmonella contamination. The product was distributed across 19 states.
Product
Black Fungus Golden Koi 2.5 oz packages 100 bags per case UPC: 81005681145 Product of China
Category
Food
Distribution
19 states
SevereFDA (Food)·F-0963-2023·2023-06-07
Bean Sprouts from Chang & Son Enterprises Recalled for Listeria Contamination
Bean sprouts produced by Chang & Son Enterprises, Inc. are recalled due to potential Listeria monocytogenes contamination. Affected products include 10-pound bags and 12-ounce packages with sell-by dates before May 28, 2023.
Product
a.) BEAN SPROUTS, 10 LBS, PRODUCT OF USA; CHANG FARM; SO.DEERFIELD, MA; KEEP REFRIGERATED; package in plastic bags b.) Nature's Wonder brand Premium BEAN SPROUTS; ALL NATURAL AND READY TO COOK; NET WT 12 oz (340 g); REFRIGERATE
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0964-2023·2023-06-07
Soybean Sprouts Recalled Due to Potential Listeria Contamination
Nature's Wonder Premium Soybean Sprouts are recalled due to potential Listeria monocytogenes contamination. Affected products (12 oz bags, UPC 815098001347) were distributed in seven states; discard or return if purchased.
Product
Nature's Wonder Premium Soybean Sprouts 12oz bag (UPC: 815098001347)
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0970-2023·2023-06-07
Organic Pineapple Chunks Recalled for Potential Listeria Contamination
SunOpta Grains and Foods Inc. is recalling Organic Pineapple Chunks due to potential Listeria monocytogenes contamination. Affected lots 8FQ229702000MX and 8FQ229802000MX were distributed in Oregon.
Product
Organic Pineapple Chunks, Item 4510-000, packed in 30 lb. poly-lined boxes.
Category
Food
Distribution
1 state
SevereFDA (Drugs)·D-0868-2023·2023-06-07
Pediatric Cough Suppressant G-SUPRESS DX Recalled Due to Product Mix-Up
G-SUPRESS DX pediatric drops are being recalled due to a product mix-up: an incorrect product was found inside some cartons in Puerto Rico. The recall affects 9,077 bottles (Lot D20911, expires Oct/25).
Product
G-SUPRESS DX — G-SUPRESS DX (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE)
Category
Drug
Distribution
0 states
SevereNHTSA·23V391000·2023-06-01
2023 Entegra Odyssey motorhomes recalled for loose rear axle bolts
Jayco is recalling certain 2023 Entegra Odyssey motorhomes because bolts securing the rear axle rotor to the wheel hub may be improperly tightened, potentially causing wheel separation and increased crash risk.
Product
ENTEGRA — 2023 ENTEGRA ODYSSEY
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·23213·2023-06-01
PowerXL Self-Cleaning Juicers recalled for laceration and ingestion hazards
Empower Brands is recalling about 469,000 PowerXL Self-Cleaning Juicers because they can rupture during use, causing cuts, or leave particle shavings in juice. The company is aware of 261 incident reports including 47 injuries.
Product
PowerXL Self-Cleaning Juicers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·23212·2023-06-01
EGO Power+ Cordless Hedge Trimmers recalled for unexpected activation and laceration risk
Chervon North America is recalling about 85,000 EGO Power+ Model HT2410 Cordless Brushless Hedge Trimmers due to a faulty rear trigger switch. The company has received 34 reports of unexpected activation, including 8 that caused lacerations requiring stitches.
Product
EGO Power+ Model HT2410 Cordless Brushless Hedge Trimmers
Category
Consumer Product
Distribution
Distributed nationwide

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3301–3325 of 6105