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

926–950 of 89448

HighFDA (Devices)·Z-2617-2026·2026-07-08
DePuy Synthes ATTUNE Revision Hinge Knee Insert Components Recall
DePuy Synthes is recalling ATTUNE Revision Hinge Knee Insert Components distributed to Minnesota, North Carolina, and Texas because external sterile packaging was found adhered to internal sterile packaging, potentially compromising sterility.
Product
Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below product descriptions and Part Codes. 1. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 10mm B; Part Number: 151730410. 2. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 12mm B; Part Number: 151730412.
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-2626-2026·2026-07-08
Boston Scientific CRE Pro Wireguided catheters recalled for packaging
Boston Scientific is recalling CRE Pro Wireguided 6-8mm 240cm catheters worldwide due to a potential sterile breach in the packaging pouches, which could compromise device sterility.
Product
CRE Pro Wireguided 6-8mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0661-2026·2026-07-08
Cinacalcet Tablets Recalled for N-Nitroso Impurity Exceeding Limits
Cipla USA, Inc. is recalling Cinacalcet Hydrochloride 30 mg tablets due to the presence of N-nitroso-cinacalcet above the acceptable daily intake. The affected product was distributed nationwide.
Product
CINACALCET — CINACALCET (CINACALCET)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2609-2026·2026-07-08
Medline Convenience Kits Containing Recalled Swan-Ganz Catheters
Medline is recalling convenience kits containing Swan-Ganz catheters due to leaks and breakage of the proximal injectate lumen hub, which may cause infection, medication loss, or blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN CABG DYNJ905855 KIT UNIVERSITY CABG PACK DYNJ905857 OH MED RN CDS DYNJ905936B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2612-2026·2026-07-08
Medline Convenience Kits with Recalled Swan-Ganz Catheters
Medline Convenience kits containing recalled Swan-Ganz catheters may leak or break at the proximal injectate lumen hub, risking infection, medication loss, and blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK CTX DYNJ68530A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2627-2026·2026-07-08
CRE Pro Wireguided 8-10mm 240cm Medical Device Sterile Pouch Breach
Boston Scientific is recalling CRE Pro Wireguided 8-10mm 240cm devices worldwide due to a potential sterile breach of the product packaging pouches. The breach could compromise the sterility of the devices.
Product
CRE Pro Wireguided 8-10mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V443000·2026-07-08
Husqvarna and GasGas Motorcycles Recalled for Brake Caliper Cracks
KTM North America is recalling certain 2022-2024 Husqvarna FE 501S, FE 350S, and 2024 GasGas ES 350 and ES 500 motorcycles due to a potential rear brake caliper crack that could reduce braking ability and increase crash risk.
Product
HUSQVARNA — HUSQVARNA, GASGAS FE 350S, ES 350, ES 500, FE 501S
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0660-2026·2026-07-08
Amphetamine extended-release capsules contain immediate-release pellets after label mix-up
Mixed amphetamine salts extended-release capsules, 5 mg, from Lannett are being recalled because the capsules contain only immediate-release pellets. 1,392 bottles affected.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SULFATE, DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE SULFATE AND AMPHETAMINE ASPARTATE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·26V442000·2026-07-08
PETERBILT 579 Tractors Recalled for Air Brake Valve Installation
PACCAR is recalling certain 2026–2027 Peterbilt 579 and 2027 Kenworth T680 tractors with a potentially incorrectly installed trailer air connection quick release valve that can cause trailer instability after braking.
Product
KENWORTH — KENWORTH, PETERBILT T680, 579
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2642-2026·2026-07-08
ARTIS Icono Ceiling Model 11328100 Loss of Movement Capability Recall
Siemens Medical Solutions is recalling 119 units of the ARTIS icono ceiling (Model 11328100) due to potential loss of movement capability when the detector lift height is adjusted to its maximum or minimum limits.
Product
ARTIS icono ceiling. Model Number: 11328100.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2670-2026·2026-07-08
Radius VSM ECG Pre-connected Set Recalled for Incorrect Heart Rate Detection
Masimo Corporation is recalling Radius VSM ECG pre-connected sets because the ECG electrode assembly may incorrectly detect extreme bradycardia or tachycardia and trigger false alarms on patients with normal heart rates, potentially distracting clinicians from true positive alarms and delaying treatment.
Product
Radius VSM ECG pre-connected Set, REF: 4842, 4695
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1129-2026·2026-07-08
MorningStar Farms Buffalo Chik'n Nuggets recalled for potential plastic contamination
MorningStar Farms Buffalo Chik'n Nuggets (10.5 oz.) are being recalled due to potential contamination with plastic material. Affected products have Best If Used By dates of JUL 07 2027 and JUL 08 2027.
Product
MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 oz. (298g), packaged in a resealable plastic bag with UPC 028989101105, packed 6 bags per case
Category
Food
Distribution
41 states
HighFDA (Devices)·Z-2623-2026·2026-07-08
GC Agar Base Culture Media Reduced Recovery of Neisseria gonorrhoeae
Remel, Inc is recalling GC Agar Base culture media because some strains of Neisseria gonorrhoeae may not be recovered or may show reduced recovery on the product.
Product
GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2647-2026·2026-07-08
RayCare 2024A SP4 Oncology System Beam Set Delivery Note Data Loss
RayCare 2024A SP4 oncology information system may lose data or fail to notify users when beam set delivery notes are modified simultaneously or updated during treatment sessions.
Product
RayCare 2024A SP4. Oncology Information Systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2608-2026·2026-07-08
Medline Convenience Kits with Recalled Swan-Ganz Catheters
Medline Industries is recalling convenience kits containing Swan-Ganz catheters due to defects in the proximal injectate lumen hub that may leak or break, risking infection, medication loss, and blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters CENTRAL AND ARTERIAL LINE TOTE DYNJ8407
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2631-2026·2026-07-08
CRE Pro Wireguided esophageal stent device recalled for packaging sterility
Boston Scientific is recalling CRE Pro Wireguided 18-20mm 240cm esophageal stents due to potential sterile breach of product pouches. The breach could allow contamination of sterile devices.
Product
CRE Pro Wireguided 18-20mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1136-2026·2026-07-08
Pepperoni Rolls Recalled for Undeclared Milk Allergen and Temperature Control Failure
Fry Pie Factory LLC is recalling pepperoni rolls (5 oz, UPC 601959803041) distributed in Ohio and West Virginia due to undeclared milk allergen and failure to maintain required refrigeration during storage.
Product
Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged in a clear plastic bag, UPC 601959803041
Category
Food
Distribution
2 states
SevereNHTSA·26V435000·2026-07-07
Wabash Recalls Econex Refrigerated Bodies Due to Detaching Steps
Wabash is recalling 2021-2026 Econex Refrigerated Bodies because side door stirrup steps may detach, increasing the risk of injury or a crash.
Product
WABASH — WABASH ECONEX REFRIGERATED BODY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V434000·2026-07-07
Braun Recalls 2026 Chevrolet Traverse Vehicles Due to Fuel Leak Risk
Braun is recalling 2026 Chevrolet Traverse vehicles because a missing braze connection on the fuel fill line may allow fuel to leak, increasing the risk of fire.
Product
BRAUN — BRAUN CHEVROLET TRAVERSE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V445000·2026-07-07
Tesla Recalls 2026 Model Y and 2024 Model 3 for Safety Noncompliance
Tesla is recalling specific 2026 Model Y and 2024 Model 3 vehicles because they lack required safety features and bumper testing. Owners will be offered a repurchase.
Product
TESLA — TESLA MODEL Y, MODEL 3
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V436000·2026-07-07
Subaru Ascent, Forester, and Crosstrek vehicles with incorrect weight labels
Subaru is recalling certain 2019–2026 Ascent, 2025–2026 Forester, and 2026 Crosstrek Hybrid vehicles due to incorrect Gross Axle Weight Rating labels, which may lead to vehicle overload and increased crash risk.
Product
SUBARU — SUBARU ASCENT, FORESTER, CROSSTREK HYBRID, FORESTER HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26E043000·2026-07-07
Harbor Freight Recalls Kenway LED Towing and Submersible Light Kits
Harbor Freight Tools is recalling specific Kenway LED towing and submersible light kits because they may not illuminate properly, increasing crash risk.
Product
EXTERIOR LIGHTING:TAIL LIGHTS:BULBS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26E042000·2026-07-06
Prime-Time Recalls 2025-2026 Ford Med Transit Vans with Wheelchair Retractions
Prime-Time Specialty Vehicles is recalling 2025-2026 Ford Med Transit vans equipped with Q'Straint Max wheelchair retractors that may fail to lock, posing an injury risk.
Product
EQUIPMENT ADAPTIVE/MOBILITY:WHEELCHAIR RESTRAINTS/SECUREMENT:CRITICAL FASTENERS recall
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-07032026-01·2026-07-03
GoodTimes beef jerky contains undeclared wheat under FSIS public health alert
FSIS has issued a public health alert for Street's Beef Jerky Teriyaki Flavor because it contains wheat, which is not declared on the label. No recall was requested.
Product
GoodTimes Beef Jerky — FSIS Issues Public Health Alert for A Ready-To-Eat Beef Jerky Product Due to Misbranding and Undeclared Allergen
Category
Food
Distribution
1 state
CriticalCPSC·26600·2026-07-02
Junpower CR2032 Lithium Coin Batteries Recalled for Ingestion Hazard
Junpower CR2032 Batteries (20-piece packs) lack required child-resistant packaging and warning labels. If swallowed, these lithium coin batteries can cause serious internal injuries or death.
Product
Junpower CR2032 Batteries
Category
Consumer Product
Distribution
Distributed nationwide

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