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

8026–8050 of 113894

ModerateFDA (Food)·H-0328-2025·2025-07-30
Gedney dill pickles slated for disposal were inadvertently sold
Gedney dill pickle products, including Whole Pickles and Mini Munchers Kosher Dill, are being recalled because product slated for disposal due to damage was inadvertently sold. 3,520 cases affected.
Product
Dill Pickles packaged under the following label: 1. Gedney Whole Pickles, item 15100, Net 32 fl oz. (1Qt)946mL. UPC 0 41660-00151 8. 2. Gedney Mini Munchers Kosher Dill, item 17100, Net 32 fl oz. (1Qt)946mL. UPC 0 41660-00171 6. 3. Gedney Kosher Dill Babies, item 17200, Net 3
Category
Food
Distribution
1 state
ModerateFDA (Food)·H-0307-2025·2025-07-30
Middle East Coast tahini dip may contain spoilage organisms
Middle East Coast brand Tahini Dip in 6 oz tubs is being recalled because the product may be contaminated with spoilage organisms. 658 tubs are affected.
Product
Middle East Coast brand Tahini Dip; NET WT: 6 OZ (170g); INGREDIENTS: TAHINI, ORGANIC LEMON JUICE, GARLIC, OLIVE OIL, SEA SALT, ORGANIC TOASTED SESAME. CONTAINS SESAME; Locally Crafted by SHOVEL AND SPOON; UPC 8 60005 50281 3
Category
Food
Distribution
3 states
ModerateFDA (Food)·H-0390-2025·2025-07-30
Herbalife Relaxation Tea made with an incorrect ingredient from the supplier
Herbalife Nutrition Relaxation Tea is being recalled because an incorrect ingredient was received from the supplier and used in manufacturing the finished product. 5,888 units are affected.
Product
Herbalife Nutrition, Relaxation Tea, Net Wt: 1.69 OZ (48g) UPC# L044KUS0A-00
Category
Food
Distribution
0 states
ModerateFDA (Devices)·Z-2142-2025·2025-07-30
Ellik Evacuator male connector tubing has conflicting sterilization instructions in Japan
The Tubing for Male Connector 194, Ellik Evacuator, model 190-4, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU.
Product
Tubing for Male Connector 194, Ellik Evacuator. Model Number: 190-4. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
Category
Medical Device
Distribution
0 states
ModerateFDA (Drugs)·D-0538-2025·2025-07-30
Prolia prefilled syringes recalled after potential temperature excursions during transit delays
Prolia (denosumab) injection 60 mg/mL is being recalled because of CGMP deviations involving potential temperature excursions due to transit delays. 6 pre-filled syringes are affected.
Product
PROLIA — PROLIA (DENOSUMAB)
Category
Drug
Distribution
3 states
ModerateFDA (Drugs)·D-0540-2025·2025-07-30
Benlysta vials recalled after potential temperature excursions during transit delays
Benlysta (belimumab) for injection 400 mg/20 mL is being recalled because of CGMP deviations involving potential temperature excursions due to transit delays. 3 vials are affected.
Product
BENLYSTA — BENLYSTA (BELIMUMAB)
Category
Drug
Distribution
3 states
ModerateFDA (Devices)·Z-2157-2025·2025-07-30
EasiSlush sterile slush solution missed a quarterly gamma sterilization dose audit
Bridge to Life EasiSlush is being recalled because quarterly dose audits monitoring the gamma sterilization process were not completed on time for three lots in the first quarter of 2024. 4,528 units affected.
Product
Bridge to Life EasiSlush, (Sodium Chloride Solution for Sterile Slush Preparation) (0.9% Sodium Chloride Irrigation, USP), Part Number REF BTLE-1250
Category
Medical Device
Distribution
16 states
ModerateFDA (Drugs)·D-0537-2025·2025-07-30
Clomipramine capsules failed a degradation product specification at expiry testing
Clomipramine Hydrochloride Capsules USP 25 mg are being recalled after an out of specification result for an unspecified degradation product during retention sample testing at expiry. 2,724 bottles affected.
Product
CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE CAPSULES)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0539-2025·2025-07-30
Evenity prefilled syringes recalled after potential temperature excursions during transit delays
Evenity (romosozumab-aqqg) injection 105 mg/1.17 mL is being recalled because of CGMP deviations involving potential temperature excursions due to transit delays. 2 pre-filled syringes affected.
Product
EVENITY — EVENITY (ROMOSOZUMAB-AQQG)
Category
Drug
Distribution
3 states
ModerateFDA (Devices)·Z-2140-2025·2025-07-30
Green endoscope silicone seals have conflicting sterilization instructions in Japan
Green Silicone Seals for Accessories, reusable 0-7 FR, model CS-G7, are being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU.
Product
Green Silicone Seal for Accessories, Reusable Silicone Seal 0 - 7 FR. Model Number: CS-G7. The reusable silicone seals fit over the biopsy port of endoscopes to seal off the working channel. Some contain a lumen which allows instruments to be passed through the seal and mini
Category
Medical Device
Distribution
0 states
ModerateFDA (Drugs)·D-0536-2025·2025-07-30
Compounded quadruple ophthalmic solution returned subpotent assay results in stability testing
A compounded Tropicamide-Proparacaine-Phenylephrine-Ketorolac sterile ophthalmic solution is being recalled because of subpotent assay results during stability testing. 2,890 vials are affected.
Product
Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5mL, 2x5ML vial per carton, Rx Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-733-05.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2143-2025·2025-07-30
Ellik Evacuator recalled over conflicting sterilization instructions in Japanese inserts
The Ellik Evacuator, model 194, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU. 11 units are affected.
Product
Ellik Evacuator. Model Number: 194. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2163-2025·2025-07-30
ACUVUE OASYS MAX multifocal daily lenses have bubbles and voids
ACUVUE OASYS MAX 1-Day MULTIFOCAL contact lenses are being recalled because of defects, specifically bubbles and voids, identified during standard finished goods testing. 114,165 lenses affected.
Product
ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2141-2025·2025-07-30
Ellik Evacuator glass body has conflicting sterilization instructions in Japan
The Glass Body for the 194 Ellik Evacuator, model 190A, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU.
Product
Glass Body For 194 Ellik Evacuator. Model Number: 190A. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
Category
Medical Device
Distribution
0 states
SevereNHTSA·25V495000·2025-07-29
Mack Recalls 2026 Granite Trucks Due to Brake Drum Incompatibility
Mack Trucks is recalling 2026 Granite GR trucks because incompatible brake drums and steer axles may cause loss of brake function, increasing crash risk.
Product
MACK — MACK GRANITE GR (4)
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25E046000·2025-07-29
Terran Industries Recalls 7000lb Axle Assemblies Due to Suspension Defect
Terran Industries is recalling 7000lb axle assemblies because incorrect suspension components may have been installed, posing a risk of axle spring failure or wheel detachment.
Product
SUSPENSION:MULTIPLE AXLE recall
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·027-2025·2025-07-29
Ada Valley Recalls Frozen Ground Beef Due to Metal Contamination
Ada Valley Meat Company is recalling approximately 1,065 pounds of fully cooked frozen ground beef due to possible metal contamination. The products were distributed to five states.
Product
Ada Valley Gourmet Foods — Ada Valley Meat Company Recalls Ready-To-Eat Ground Beef Products Due to Possible Foreign Matter Contamination
Category
Food
Distribution
5 states
SevereNHTSA·25V494000·2025-07-28
Kia Telluride door belt molding trim can delaminate and detach
Kia is recalling certain 2023-2025 Telluride vehicles because the door belt molding trim can delaminate and detach from the vehicle, becoming a road hazard.
Product
KIA — KIA TELLURIDE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V493000·2025-07-28
Kia K5 rear window trim pieces may loosen and detach
Kia is recalling certain 2023-2025 K5 vehicles because the left and right rear window trim pieces may loosen and detach, becoming a road hazard for other vehicles.
Product
KIA — KIA K5
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V492000·2025-07-28
Porsche Recalls 2024-2025 Macan 4 Electric for Air Bag Defect
Porsche is recalling 2024-2025 Macan 4 Electric vehicles because front seat air bags may be improperly secured, potentially preventing proper deployment during a crash.
Product
PORSCHE — PORSCHE MACAN 4 ELECTRIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V491000·2025-07-28
Grech motorhome awnings can extend unintentionally during transit
Grech Motors is recalling certain 2020-2025 Strada, Turismo and Terreno motorhomes because the retractable awning may extend unintentionally while the vehicle is moving.
Product
GRECH — GRECH STRADA, TURISMO, TERRENO
Category
Vehicle
Distribution
Distributed nationwide
ModerateNHTSA·25V490000·2025-07-28
2026 Tesla Model Y vehicles recalled for inoperable horn
Tesla is recalling certain 2026 Model Y vehicles because the horn ground wire ring terminal may be improperly secured, causing the horn to fail. An inoperable horn increases the risk of crashes.
Product
TESLA — TESLA MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-07272025-01·2025-07-27
USDA Alerts on Ham Salad Products with Recalled Breadcrumbs
USDA FSIS issued a public health alert for Reser's and Molly's Kitchen ham salad products containing breadcrumbs recalled for possible Listeria monocytogenes contamination.
Product
Reser's Fine Foods, Inc. — FSIS Issues Public Health Alert For Ready-To-Eat Ham Salad Products Containing FDA-Regulated Breadcrumbs That Have Been Recalled Due to Possible Listeria Monocytogenes Contamination
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·25V486000·2025-07-25
Forest River Recalls 2025-2026 Motorhomes Due to Fuel Line Fire Risk
Forest River is recalling 2025-2026 Sunseeker, Solera, and other motorhomes because fuel line connectors may detach, creating a fire hazard.
Product
FOREST RIVER — FOREST RIVER, EAST TO WEST SUNSEEKER, FREELANDER, LEPRECHAUN, FORESTER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V488000·2025-07-25
Ford electronic brake booster can fail losing power brake assist
Ford is recalling certain 2025 Lincoln Navigator, F-150, Expedition, Bronco and Ranger vehicles because the Electronic Brake Booster module may malfunction, causing a loss of power brake assist.
Product
FORD — FORD, LINCOLN F-150, EXPEDITION, BRONCO, RANGER
Category
Vehicle
Distribution
Distributed nationwide

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8026–8050 of 113894