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

18526–18550 of 39605

SevereFDA (Devices)·Z-1139-2018·2018-03-28
BD Vacutainer Tubes Recalled for Lead Test Inaccuracy
Becton Dickinson is recalling specific Vacutainer tubes because they may cause underestimation of lead levels in blood samples when used with certain assays.
Product
BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 (UDI: 50382903664011); 2. 366450 (UDI: 50382903664509); 3. 366643 (UDI: 50382903666435); 4. 367835 (UDI: 50382903678353); 5. 367841 (UDI: 50382903678414); 6. 367844 (UDI: 50382903678445); 7. 367856 (UDI…
Category
Medical Device
Distribution
47 states
SevereFDA (Devices)·Z-1133-2018·2018-03-28
Boston Scientific Recalls SpyScope DS Biliary Catheters Due to Sleeve Defect
Boston Scientific is recalling 5,026 units of SpyScope DS Access and Delivery diagnostic biliary catheters because a sleeve may protrude, causing tissue damage or bleeding.
Product
SpyScope DS Access and Delivery diagnostic biliary catheter, M00546600
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1075-2018·2018-03-28
Iridex TruFocus LIO Premiere Laser Indirect Ophthalmoscope Recalled for Misdirected Energy
Iridex Corporation is recalling the TruFocus LIO Premiere Laser Indirect Ophthalmoscope because laser energy was not directed as intended, causing focal cataracts and iris burns.
Product
Iridex TruFocus LIO Premiere" Laser Indirect Ophthalmoscope ( LIO ) The LIO is a headmounted indirect ophthalmoscope which is used with a handheld lens to view and perform laser treatments on a patient s retina. It allows binocular visualization of the peripheral retina…
Category
Medical Device
Distribution
0 states
SevereUSDA FSIS·026-2018·2018-03-28
Tony Downs Recalls Chicken Products Due to Possible Plastic Contamination
Tony Downs Foods is recalling approximately 96,384 pounds of canned chicken breast products that may contain hard plastic. The recall was initiated after two consumer complaints regarding foreign matter.
Product
Tony Downs Foods — Tony Downs Food Company, Inc. Recalls Chicken Products due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
SevereCPSC·18732·2018-03-28
Shop LC Recalls Electric Blankets Due to Fire and Burn Hazards
Shop LC is recalling electric heated throw blankets because the heating coils can overheat, posing fire and burn hazards.
Product
Electric heated micro plush flannel sherpa throw blankets
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Food)·F-1000-2018·2018-03-28
Guixens Food Group Recalls Dried Yellow Potatoes for Undeclared Sulfites
Guixens Food Group, Inc. is recalling La Marinera Dried Yellow Potatoes because the product contains undeclared sulfites, a common allergen.
Product
La Marinera, Dried Yellow Potatoes-Papa seca amarilla, NET WEIGHT 10oz (283.5gr.), Imported/Distributed by: Guixens Food Group, Inc., Expiration date: July 2018
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1141-2018·2018-03-28
BD Vacutainer Tubes Recalled for Lead Test Inaccuracy
Becton Dickinson is recalling specific Vacutainer tubes because they may cause underestimation of lead in blood samples when used with certain assays.
Product
BD Vacutainer¿ EDTA Pink Top Tube; Catalog Numbers: 1. 367842 (UDI: 50382903678421); 2. 367899 (UDI: 50382903678995); 3. 368049 (UDI: 50382903680493); 4. 368589 (UDI: 50382903685894)
Category
Medical Device
Distribution
47 states
SevereFDA (Food)·F-0996-2018·2018-03-28
Avalon Packaging Recalls NXTGEN Kratom Due to Salmonella Risk
Avalon Packaging is recalling NXTGEN Kratom dietary supplements due to the potential for Salmonella contamination. The affected product consists of 1,108 bottles of 70 capsules each.
Product
NXTGEN Botanicals, Maeng Da Kratom, Dietary Supplement, 70 Capsules, Made in the U.S.A
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-0194-2018·2018-03-28
Monteris Medical Recalls NeuroBlate Systems Due to MRI Interaction
Monteris Medical Corp is recalling 52 NeuroBlate systems used for MRI-guided neurosurgery due to an unanticipated interaction with 1.5 Tesla MRI systems.
Product
MONTERIS MEDICAL NEUROBLATE SYSTEM, used for MRI-guided neurosurgical ablation.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1123-2018·2018-03-28
MedComp Recalls 12F Modified Tesio Catheter Sets Due to Connection Failures
Medical Components, Inc. is recalling 40 kits of 12F Modified Tesio Catheter Sets because connection failures could cause blood loss or air emboli.
Product
12F MODIFIED Tesio CATHETER SET, REF MCTC1235SM, UDI 884908027259 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1142-2018·2018-03-28
BD Vacutainer Tubes Recalled for Lead Test Inaccuracy
Becton Dickinson is recalling specific Vacutainer tubes because they may cause underestimation of lead levels in blood samples when used with certain assays.
Product
BD Vacutainer¿ Lithium Heparin Green Top Tube; Catalog Numbers: 1. 366664 (UDI: 50382903666640); 2. 367884 (UDI: 50382903678841); 3. 367886 (UDI: 50382903678865); 4. 368040 (UDI: 50382903680400); 5. 366667 (UDI: 50382903666671); 6. 367880 (UDI: 50382903678803)
Category
Medical Device
Distribution
47 states
SevereFDA (Devices)·Z-1119-2018·2018-03-28
MedComp Repair Kit Recalled for Potential Connection Failures
Medical Components, Inc. is recalling 5 MedComp Repair Kits due to potential connection failures that could cause blood loss or air emboli.
Product
REPAIR KIT, REF ARA101, UDI 884908083637 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1140-2018·2018-03-28
BD Vacutainer Tubes Recalled for Lead Test Inaccuracy
Becton Dickinson is recalling specific Vacutainer tubes because they may cause underestimation of lead levels in blood samples when used with certain assays.
Product
BD Vacutainer¿ EDTA Tan Top Tube; Catalog Number: 367855 (UDI: 50382903678551)
Category
Medical Device
Distribution
47 states
SevereFDA (Food)·F-0935-2018·2018-03-28
Weis Dried Beef Party Rye Dip Recalled for Undeclared Allergens
Weis Markets is recalling Dried Beef Party Rye Dip because the label failed to list egg and milk, which are present in the ingredients.
Product
Dried Beef Party Rye Dip; Ingredients: Hellman's Mayonaise, Sour Cream, Dried Beef (Cured with Water, Salt, Sugar, Sodium Nitrate, Sodium Nitrite), Parsley, Onion, Dill Weed; SELL BY date up to 3/11/18
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0939-2018·2018-03-28
ASR Group Recalls Tank Truck Medium Invert Syrup Due to Metal
ASR Group International Inc. is recalling approximately 50,000 wet pounds of Tank Truck Medium Invert Syrup because it may contain foreign metal material.
Product
Tank Truck Medium Invert Syrup (403777)
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-1104-2018·2018-03-28
Boston Scientific Recalls Malecot Nephrostomy Catheters Due to Mid-Shaft Breakage
Boston Scientific is recalling certain Malecot Nephrostomy Catheters because they are breaking at the mid-shaft bond during use.
Product
Percutaneous Access Set, Product Number: M0064201150, GTIN: 08714729009757 The Malecot Nephrostomy Catheter Set is intended to establish percutaneous nephrostomy drainage and is indicated for the following: Diagnostic Indications: " Antegrade pyelography " Pressure/perfusion…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·18V200000·2018-03-28
Toyota Recalls 2018 Camry Vehicles Due to Engine Piston Defect
Toyota is recalling 2018 Camry vehicles with 2.5L engines because oversized pistons may cause the engine to stall, increasing crash risk.
Product
TOYOTA — TOYOTA CAMRY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V198000·2018-03-27
Newmar Recalls Motorhomes Due to Power Steering Hose Routing Defect
Newmar is recalling 2011-2017 Mountain Aire, Dutch Star, and Ventana motorhomes because the power steering hose may rub against the starter motor, causing fluid leaks or electrical arcing.
Product
NEWMAR — NEWMAR MOUNTAIN AIRE, DUTCH STAR, VENTANA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V195000·2018-03-26
Polaris Recalls 2015-2018 Slingshot Motorcycles Due to Seat Belt Weld Defect
Polaris is recalling 2015-2018 Slingshot motorcycles because improperly welded seat brackets may fail, increasing crash injury risk.
Product
POLARIS — POLARIS SLINGSHOT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V191000·2018-03-26
Western Star Trucks Recalled for Electrical Arc Fire Risk
Daimler Trucks North America is recalling 2017-2019 Western Star trucks because a power stud may contact the bulkhead, causing an electrical arc that increases fire risk.
Product
WESTERN STAR — WESTERN STAR 6900, 4900, 4700, 5700
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V192000·2018-03-26
Thomas Built Buses Recall School Buses Due to Seat Bracket Crack Risk
Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses school buses because a wall mounting bracket may crack, causing seats to detach in a crash.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX, MINOTOUR, SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V190000·2018-03-26
Thomas Built Buses Saf-T-Liner C2 Propane Leak Recall
Daimler Trucks North America is recalling 2014-2019 Thomas Built Buses Saf-T-Liner C2 school buses with propane engines due to a fuel line chafing risk that could cause a leak and fire.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V193000·2018-03-26
Thomas Built Buses Recall Transit Models Due to Seat Bracket Defect
Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses transit models because a wall mounting bracket may crack, increasing injury risk in a crash.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX, SAF-T-LINER C2, MINOTOUR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V188000·2018-03-23
Ferrari Recalls 458 Italia and California Models for Air Bag Defect
Ferrari is recalling 2009-2011 California and 2010-2011 458 Italia vehicles because passenger air bag inflators may explode during a crash, posing a risk of serious injury or death.
Product
FERRARI — FERRARI 458 ITALIA, CALIFORNIA
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0971-2018·2018-03-21
Starwest Botanicals Recalls Organic Cardamom Pods Due to Salmonella Risk
Starwest Botanicals is recalling organic cardamom pods after a customer reported a positive Salmonella test result for a specific bulk lot.
Product
Cardamom Pods Green Whole Organic Sold in 25 lb. bulk boxes and 1 lb. retail plastic bags UPC 1 pound bags: 7-6796302528-9; UPC bulk: 7 679630257-2 Imported from Guatemala Starwest Botanicals, Sacramento, CA
Category
Food
Distribution
0 states

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18526–18550 of 39605