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

2476–2500 of 39705

SevereFDA (Devices)·Z-2083-2025·2025-07-16
FEM-FLEX II femoral arterial cannulas may have wire protruding from body
Edwards FEM-FLEX II Femoral Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 847 units affected.
Product
Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016AS Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2082-2025·2025-07-16
FEM-FLEX II FEMII016A cannulas may have wire protruding from body
Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII016A, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 6,801 units affected.
Product
Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V470000·2025-07-16
BMW electric vehicle battery modules may be improperly assembled
BMW is recalling certain 2022-2025 iX, 2023-2024 i7 and 2022-2023 i4 vehicles because high-voltage battery cell modules may not have been assembled properly, stressing the module frame.
Product
BMW — BMW I4, I7, IX
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2047-2025·2025-07-16
Bravo CF capsule delivery devices may have misapplied adhesive causing malfunction
The Bravo CF capsule delivery device is being recalled because misapplied adhesive may prevent the pH capsule attaching to the oesophagus or detaching from the delivery device. 128,202 units affected.
Product
Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guidance, Product Number FGS-0635 (5 pack) and FGS-0636 (1 pack)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0213-2025·2025-07-16
JLM dark chocolate nonpareils recalled over undeclared milk allergen
JLM Manufacturing Dark Chocolate Nonpareils in 14 oz tubs are being recalled because of undeclared milk. 971 cases are affected, distributed nationwide.
Product
JLM Manufacturing Dark Chocolate Nonpareils, 14oz clear plastic tub, UPC 7 60208 12450 1, item # 392303, 12 retail units per wholesale case
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-0214-2025·2025-07-16
Garlic cheddar cheese curds recalled over potential Listeria monocytogenes contamination
Vampire Slayer Garlic Cheddar Cheese Curds are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 260 cases are affected.
Product
VAMPIRE SLAYER Garlic Cheddar Cheese Curds, net wt. 6 oz. Product is package in a sealed plastic cup with lid. UPC on 6oz. retail cup: 8 51222 00528 7. FaceRockCreamery.com MASTER CASE's label is read in parts: Item No. 240062 Vampire Slayer Curds 12/6oz., net wt. 4.5 lbs. Face…
Category
Food
Distribution
2 states
SevereFDA (Food)·H-0216-2025·2025-07-16
Weaver white seed nonpareil chocolate recalled over undeclared milk allergen
Weaver Chocolates Nonpareil Semi-Sweet Chocolate (White Seeds) in 25 lb bulk cases is being recalled because of an undeclared milk allergen. 1,760 cases are affected.
Product
Weaver Chocolates, D2645 - Nonpareil, Semi-Sweet Chocolate (White Seeds) - 25 lbs. Bulk Cases
Category
Food
Distribution
14 states
SevereNHTSA·25T013000·2025-07-15
Continental Recalls General Tire Altimax RT45 Tires Due to Sidewall Defect
Continental Tire is recalling 542 General Tire Altimax RT45 tires that may have been overcured, posing a risk of tread separation or sidewall breakage.
Product
TIRES:SIDEWALL recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V415000·2025-07-15
Porsche suspension strut retaining ring can loosen dislodging the strut
Porsche is recalling certain 2025 Panamera, Panamera E-Hybrid and Taycan vehicles because a retaining ring on top of the suspension strut may come loose, dislodging the strut and losing air from the spring.
Product
PORSCHE — PORSCHE TAYCAN, PANAMERA, PANAMERA 4 E-HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V468000·2025-07-14
AMO Recalls 2025 Utility Trailers Due to Axle Separation Risk
American Manufacturing Operations is recalling 2025 AMO Utility trailers because shackle nuts may loosen, allowing the axle to detach and increasing crash risk.
Product
AMO — AMO UTILITY TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V467000·2025-07-11
Ford Bronco Sport and Escape fuel injectors may crack and leak
Ford is recalling certain 2021-2024 Bronco Sport and 2020-2022 Escape vehicles with 1.5L engines because a fuel injector may crack and leak fuel inside the engine compartment. 694,271 vehicles affected.
Product
FORD — FORD BRONCO SPORT, ESCAPE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V459000·2025-07-11
Zero Motorcycles Recalls 2024 Models Due to Front Brake Hose Defect
Zero Motorcycles is recalling 2024 DSR/X, DS, DSR, and DSRP motorcycles because a twisted front brake hose may leak fluid and reduce braking ability.
Product
ZERO — ZERO DSRP, DSR, DS, DSR/X
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V465000·2025-07-11
Malibu Boats Recalls Triple Axle Boat Trailers Due to Brake Line Fracture Risk
Malibu Boats is recalling 2021-2026 Triple Axle Boat Trailers because a brake line may fracture, causing a loss of brake function and increasing crash risk.
Product
MALIBU BOATS — MALIBU BOATS TRIPLE AXLE BOAT TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·25377·2025-07-10
Ozark Trail 64 ounce water bottle lids can forcefully eject
Ozark Trail 64 oz Stainless Steel Insulated Water Bottles are being recalled because the lid can forcefully eject on opening. Three injuries are reported, including two cases of permanent vision loss.
Product
Ozark Trail 64 oz Stainless Steel Insulated Water Bottles
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·25V462000·2025-07-10
Mitsubishi Fuso Rizon Trucks Recalled for Electric Parking Brake Fire Risk
Mitsubishi Fuso is recalling 2024-2025 Rizon trucks because an oversized spacer in the electric parking brake may cause overheating and fire.
Product
MITSUBISHI FUSO — MITSUBISHI FUSO RIZON FECXK (E18), RIZON FEC9K (E18), RIZON FEC7K (E16)
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0202-2025·2025-07-09
Harris Teeter Sushi Recalled Over Possible Salmonella Contamination
Harris Teeter is recalling ZENSHI HANDCRAFTED SUSHI California Rolls due to possible Salmonella contamination from recalled cucumbers used in production.
Product
ZENSHI HANDCRAFTED SUSHI California Roll 10pc (Brown Rice) Net Wt. 7.1oz UPC 0 23012 94265 6 & UPC 0 23012 95137 5
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0208-2025·2025-07-09
Bibimbap Bowl recalled due to potential Salmonella contamination
JFE Franchising Inc is recalling 13 oz Bibimbap Bowls (UPC 63912389259) because cucumbers in the product have the potential to be contaminated with Salmonella.
Product
Bibimbap Bowl 13 oz 63912389259
Category
Food
Distribution
7 states
SevereFDA (Food)·H-0140-2025·2025-07-09
Harris Teeter ZENSHI Handcrafted Sushi Crunchy Dragon Roll Recalled for Salmonella
Harris Teeter is recalling ZENSHI HANDCRAFTED SUSHI Crunchy Dragon Roll (10pc, 9.6oz) due to possible Salmonella contamination from recalled cucumbers used in the product.
Product
ZENSHI HANDCRAFTED SUSHI Crunchy Dragon Roll 10pc Net Wt. 9.6oz UPC 0 23012 94461 2
Category
Food
Distribution
8 states
SevereFDA (Drugs)·D-0503-2025·2025-07-09
Lidocaine HCL Sterile Injection recalled for sterility assurance concerns
Tailstorm Health INC is recalling Lidocaine HCL Sterile Injection (20 mg/mL) due to FDA inspection findings of concerns with the sterile manufacturing process. The recalled product is distributed nationwide.
Product
LIDOcaine HCL Sterile Injection, USP, 20 mg/mL, 2%, (200 mg/10 mL), For Infiltration & Nerve Block, Including Caudal & Epidural Use, Preservative Free, 10mL Sterile Single-Dose Vial, Rx Only, Medivant Healthcare, 158 S. Kyrene Rd., Chandler, AZ, 85226, NDC 81483-0001-0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0160-2025·2025-07-09
Harris Teeter Zenshi Handcrafted Sushi First Down Platter Salmonella Recall
Harris Teeter is recalling Zenshi Handcrafted Sushi First Down Platter (19.7oz) because cucumbers used in the sushi were recalled due to possible Salmonella contamination.
Product
ZENSHI HANDCRAFTED SUSHI First Down Platter Net Wt 19.7oz UPC 0 23012 94150 5
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0137-2025·2025-07-09
ZENSHI Handcrafted Sushi Cream Cheese Roll Tuna recalled for Salmonella
Harris Teeter is recalling ZENSHI Handcrafted Sushi Cream Cheese Roll - Tuna because the cucumbers used in the product were recalled due to possible Salmonella contamination.
Product
ZENSHI HANDCRAFTED SUSHI Cream Cheese Roll - Tuna 10pc Net Wt 7.1oz UPC 0 23012 95039 2
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0192-2025·2025-07-09
Harris Teeter ZENSHI Handcrafted Sushi Spicy Roll Tuna Salmonella Recall
Harris Teeter is recalling ZENSHI HANDCRAFTED SUSHI Spicy Roll - Tuna 10pc (Brown Rice) due to possible Salmonella contamination from recalled cucumbers used in the product.
Product
ZENSHI HANDCRAFTED SUSHI Spicy Roll - Tuna 10pc (Brown Rice) Net Wt. 7.1oz UPC 0 23012 94319 6 & UPC 0 23012 95149 8
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0168-2025·2025-07-09
ZENSHI Handcrafted Sushi Hawaiian Roll Tuna recalled for Salmonella
Harris Teeter is recalling ZENSHI Handcrafted Sushi Hawaiian Roll - Tuna (10pc, 11.6oz) due to possible Salmonella contamination from recalled cucumbers used in the product.
Product
ZENSHI HANDCRAFTED SUSHI Hawaiian Roll - Tuna 10pc Net Wt. 11.6oz UPC 0 23012 94369 1
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0133-2025·2025-07-09
ZENSHI Handcrafted Sushi Classic Crab Roll Sushi Recalled for Salmonella
Harris Teeter is recalling ZENSHI Handcrafted Sushi Classic Crab Roll (10.5 oz) because cucumbers used to make the sushi were recalled due to possible Salmonella contamination.
Product
ZENSHI HANDCRAFTED SUSHI Classic Crab Roll Sushi Net Wt. 10.5oz UPC 0 23012 00702 7
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0173-2025·2025-07-09
Harris Teeter ZENSHI Handcrafted Sushi Hybrid Roku Tray Recalled for Salmonella
Harris Teeter is recalling ZENSHI Handcrafted Sushi Hybrid Roku Tray (82pc, 88.6oz) due to possible Salmonella contamination from recalled cucumbers used in the sushi.
Product
ZENSHI HANDCRAFTED SUSHI Hybrid Roku Tray 82pc Net Wt. 88.6oz UPC 0 23012 94259 5
Category
Food
Distribution
8 states

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