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

11626–11650 of 27718

HighFDA (Devices)·Z-2417-2024·2024-07-31
Call station devices may fail to transmit emergency alarms to staff
Securitas Healthcare's Arial Call Station (models CSK200 and CSK200MR) may fail to transmit alarms and experience premature battery depletion. The FDA recall affects 1,268 units distributed in the U.S. and Canada.
Product
Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery-operated call device installed inside resident living areas to allow immediate staff response.
Category
Medical Device
Distribution
9 states
HighFDA (Devices)·Z-2428-2024·2024-07-31
Beckman Coulter Clinical Reagent Recalled Due to Incorrect Lipemia Check Settings
Beckman Coulter has recalled 13,565 units of IGM clinical reagent due to incorrect lipemia check settings that may produce false low results or report high results as normal. Affected units were distributed worldwide.
Product
Beckman Coulter, REF: OSR61173, IGM 4x14 mL R1, 4x11 mL R2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2432-2024·2024-07-31
Abbott Infinity 7 Implantable Pulse Generators Recalled for Potentially Shortened Service Life
Abbott is recalling 1198 Infinity 7 Implantable Pulse Generators due to potentially incorrect service life indicators and end-of-service dates in product labeling, which could result in loss of therapy.
Product
Abbott Infinity 7, Implantable Pulse Generator, REF: 6663, SterileEO, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2418-2024·2024-07-31
Wireless Nurse Call Station Recalled for Potential Alarm Communication Failure
Arial Call Station wireless nurse call systems (models CSK200-1069 and CSK200-1069MR) are recalled due to risk of alarm communication failure and premature battery depletion. 77 units affected across multiple U.S. states.
Product
Arial Call Station, Model Numbers CSK200-1069 and CSK200-1069MR, is a wireless nurse call station.
Category
Medical Device
Distribution
13 states
HighFDA (Food)·F-1490-2024·2024-07-31
Organic Aussie Bites recalled for undeclared gluten content
Best Express Foods is recalling Universal Bakery Organic Aussie Bites due to undeclared gluten. Products labeled as gluten-free were found to contain gluten above regulatory limits.
Product
Universal Bakery Organic Aussie Bites, 30 oz clamshell container USDA Organic Certified Gluten Free Rolled Oats, Dried Apricots, Flax Seeds, Sunflower Seeds, Honey, Coconut, Quinoa, Chia Seeds + More! INGREDIENTS: Organic Rolled Oats, Organic Oat Flour, Organic Invert Cane Sugar
Category
Food
Distribution
13 states
HighFDA (Drugs)·D-0617-2024·2024-07-31
Venlafaxine Hydrochloride extended-release capsules recalled for failed dissolution specifications
Zydus Pharmaceuticals (USA) Inc. is recalling Venlafaxine Hydrochloride Extended-Release Capsules USP 37.5mg due to failed dissolution specifications in lots M213175 and M213176. The recall affects 13,128 and 252 bottles distributed nationwide.
Product
VENLAFAXINE HYDROCHLORIDE — VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2434-2024·2024-07-31
Perfusor Space Syringe Pump Recalled Due to Monoject Syringe Incompatibility
B Braun Medical's Perfusor Space Syringe Pump may not properly recognize Cardinal Health Monoject syringes due to manufacturing changes, risking medication overdose, underdose, or therapy delays.
Product
Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Wireless Model/Catalog Number: 8713031U Software Version: 8713031U Product Description: Perfusor Space Syringe Pump, Infusion Pump, 1 each Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2438-2024·2024-07-31
Sensis Vibe diagnostic systems software crash during event documentation
Siemens Sensis Vibe diagnostic systems may crash when using documentation features during once-per-study event reporting. Three systems are affected; no injuries reported.
Product
Sensis Vibe systems with software version VD15B in combination with Sensis High End Server -Intended to be used as a diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radiology as wel
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2424-2024·2024-07-31
BD Nano 2nd Gen Pen Needles recalled for post-expiration distribution
Embecta Corp. is recalling BD Nano 2nd Gen Pen Needles that were distributed at or after their February 29, 2024 expiration date. Using expired needles cannot guarantee sterility and integrity.
Product
BD Nano 2nd Gen Pen Needles 32G X 4mm (5-count sample contained in Patient Counseling Sample Toolbox -Catalog 6484755/Lot Number: 3750144)-Sterile, single use devices designed for the parenteral administration of a drug from a cartridge contained in a drug pen injector Model/C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2436-2024·2024-07-31
Perfusor Space infusion pump syringe incompatibility may cause dosing error
B Braun is recalling Perfusor Space infusion pump kits because Cardinal Health Monoject syringes have manufacturing changes that make them incompatible, potentially causing overdose, underdose, or delayed therapy.
Product
Brand Name: Perfusor Space Product Name: PERFUSOR SPACE ACM-KIT Model/Catalog Number: 8713040U Product Description: Perfusor Space, Infusion Pump Kit, 1 each Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2433-2024·2024-07-31
Infusion Pump Syringe Compatibility Issue May Cause Overdose or Underdose
B Braun is recalling Perfusor Space infusion pumps due to syringe compatibility issues with Cardinal Health Monoject syringes. The incompatibility may cause overdose, underdose, therapy delays, and alarm failures.
Product
Brand Name: Perfusor Space Product Name: Perfusor Space Infusion Pump System Model/Catalog Number: 8713030U Product Description: Perfusor Space Infusion Pump System, Infusion Pump, 1 each Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·24321·2024-07-25
Hover-1 Dynamo E-Scooters Recalled Due to Brake Failure Risk
DGL Group is recalling about 4,200 Hover-1 Dynamo e-scooters sold on Walmart.com from November 2021 through July 2022 because the brakes can fail, creating a serious injury and crash hazard. The company has received 22 reports of brake failure resulting in seven injuries.
Product
Hover-1 Dynamo E-scooters
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24315·2024-07-25
Ophanie Large Pink Area Rugs Recalled for Fire Hazard
Ophanie large pink area rugs sold on Amazon violate federal flammability regulations and pose a fire hazard. About 5,200 units sold from April through June 2024 are being recalled.
Product
Ophanie Large Pink Area Rugs
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24318·2024-07-25
Victor Electric Folding Soft Bullet Toy Guns Recalled for Eye Injury Hazard
Victor Electric Folding Soft Bullet Toy Guns sold on Temu.com lack required blaze orange tips and have projectiles that fail to meet federal safety standards for toy weapons. The recalled toy guns pose an eye injury hazard to children.
Product
Victor Electric Folding Soft Bullet Toy Guns
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24316·2024-07-25
Besrey Twins Strollers Recalled for Entrapment, Fall, and Choking Hazards
Stiger Inc. is recalling about 3,045 Besrey Twins Strollers sold on Amazon due to entrapment, fall, and choking hazards that violate federal stroller safety regulations. Consumers should stop using the product immediately.
Product
Besrey Twins Strollers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24312·2024-07-25
2024 Kawasaki Mule PRO 1000 Utility Vehicles Recalled for Fire Hazard
Kawasaki is recalling approximately 19,100 units of the 2024 Mule PRO 1000 utility vehicles due to improper combustion during engine start that can pose a fire hazard. Three fires have been reported with no injuries.
Product
2024 Kawasaki Mule PRO 1000 Off-Highway Utility Vehicles
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·24311·2024-07-25
Lancaster Table & Seating Plastic Restaurant High Chairs Recalled for Fall Hazard
Clark Associates is recalling about 27,140 Lancaster Table & Seating Standard Height Plastic Restaurant High Chairs because the T-bar at the front can become loose, fall, or break off during use, posing a fall hazard to children.
Product
Lancaster Table & Seating Standard Height Plastic Restaurant High Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24313·2024-07-25
Razor Icon Electric Scooters Recalled Due to Fall Hazard
Razor is recalling about 7,300 Icon electric scooters because the downtube can separate from the floorboard during use, causing falls. The company has received 34 reports of downtube separation with two reported injuries.
Product
Razor Icon electric scooters
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24310·2024-07-25
ProForm 50 LB Adjustable Dumbbells Recalled for Weight Plate Dislodgement
iFIT Inc. is recalling ProForm Rapid Strike 50 LB Adjustable Dumbbell Sets because weight plates can dislodge during use, causing impact injuries. The firm has received eight reports of dislodgement, including three resulting in contusions and abrasions.
Product
ProForm Rapid Strike 50 LB Adjustable Dumbbell Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24317·2024-07-25
2024 Arctic Cat Mountain 600 Snowmobiles Recalled Due to Crash Hazard
Textron Specialized Vehicles is recalling about 600 of the 2024 Arctic Cat Mountain 600 Snowmobiles because a pin on the steering knuckle u-joint may not be properly installed, allowing it to come loose and cause loss of steering control.
Product
2024 Arctic Cat Mountain 600 Snowmobiles
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1483-2024·2024-07-24
Deluxe Roasted Salted Mixed Nuts recalled for undeclared peanut allergen
DSD Merchandisers recalls Deluxe Roasted Salted Mixed Nuts (Item 99651) for undeclared peanut allergen, with distribution in six western states and a sell-by date of October 9, 2024. Consumers with peanut allergies should not consume this product.
Product
Deluxe Roasted Salted Mixed Nuts ITEM NUMBER 99651 UPC: 6-51433-99651-6 SELL BY: 10/09/2024
Category
Food
Distribution
6 states
CriticalFDA (Devices)·Z-2319-2024·2024-07-24
Abiomed Impella CP with SmartAssist heart pump units recalled for failed inspection
Abiomed is recalling 9 Impella CP with SmartAssist heart pump units that failed inspection and were inadvertently released. The devices were distributed in Florida, Massachusetts, Ohio, and Texas.
Product
Impella CP with SmartAssist, Product No.: 1000080 (REF 0048-0003). left heart support blood pump
Category
Medical Device
Distribution
4 states
SevereFDA (Food)·F-1479-2024·2024-07-24
Greens products recalled for potential Listeria monocytogenes contamination
Solata Food LLC is recalling multiple brands of greens products distributed in NY, NJ, and NH due to potential Listeria monocytogenes contamination. Affected products, totaling 4,382 lbs with expiration dates of June 20–24, 2024, should not be consumed.
Product
1. Greens Solata 5050; 6x10 clamshell; UPC: 850021494766 / 2. Greens Gaia Organic 5050; 6x10 clamshell; UPC: 850021494827 / 3. Greens Gaia Organic 50/50 blend; 8x45 clamshell; UPC: 850021494919 / 4. Greens Gaia Organic 50/50; 8x45 clamshell; UPC: 850021494957 / 5. Greens Full Ci
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1485-2024·2024-07-24
Terrafina raw macadamia nuts recalled for salmonella contamination
Terrafina macadamia nuts are being recalled because they tested positive for salmonella. The product was distributed in New Jersey and New York.
Product
Terrafina, Macadamia in the Raw , Net Wt. 6oz , (170 g)
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-2321-2024·2024-07-24
Ventilation Device Handset Plug May Disconnect from Nebulizer Adapter
Baxter's Volara System SPU circuit kits may have a faulty handset plug that disconnects from the nebulizer adapter, preventing proper ventilator gas flow.
Product
Volara System. Single Patient Use (SPU) Circuit 5kit for Volara and Single Patient Use (SPU) Circuit kit for Volara. Intermittent positive pressure breathing device.
Category
Medical Device
Distribution
Distributed nationwide

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11626–11650 of 27718