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

7151–7175 of 7514

SevereFDA (Drugs)·D-0795-2021·2021-09-22
Florance Morris Hand Sanitizer Recalled for Methanol Contamination
Florance Morris ANTISEPTIC Hand Sanitizer (70% ethyl alcohol) distributed nationwide is recalled due to FDA-detected methanol contamination and insufficient ethanol content. The product was distributed by Asimex International LLC in Florida.
Product
Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%), packaged in a) 8.45 fl oz (250 mL) bottles and b) 33.81 fl oz (1L) bottles, Distributed by: Asimex International LLC, 9100 S Dadeland Blvd, Ste 912, Miami, FL 33156, COUNTRY OF ORIGIN: MEXICO.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0975-2021·2021-09-22
Purim Health Products EpiGenius Kids Creamy Chocolate Recalled for Undeclared Milk
Purim Health Products EpiGenius Kids Creamy Chocolate powder is recalled due to undeclared milk in an MCT powder ingredient. The product was not labeled to indicate the presence of milk, which is a common allergen.
Product
Purim Health Products: EpiGenius Kids Creamy Chocolate; 630 Grams, individually packed pouches. Daily Superfoods. This high protein, whole-food blend is an excellent source of vitamins A, C, D and E and contains superfruits and superveggies, along with healthy fat, fiber and
Category
Food
Distribution
0 states
SevereFDA (Drugs)·D-0796-2021·2021-09-22
Florance Morris ANTISEPTIC Hand Sanitizer Recalled for Methanol Contamination
Florance Morris ANTISEPTIC Hand Sanitizer (70% ethyl alcohol) in 8.45 fl oz and 33.81 fl oz bottles is being recalled due to methanol contamination found in some lots. All lots are affected due to manufacturing under the same conditions as contaminated products.
Product
Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%), packaged in a) 8.45 fl oz (250 mL) bottles and b) 33.81 fl oz (1L) bottles, Distributed by: Asimex International LLC, 9100 S Dadeland Blvd, Ste 912, Miami, FL 33156, COUNTRY OF ORIGIN: MEXICO.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0805-2021·2021-09-22
AMINOSYN II 15% Amino Acid Injection Recalled for Particulate Matter
ICU Medical Inc is recalling AMINOSYN II 15% An Amino Acid Injection due to the presence of particulate matter including fibers, hair, and proteinaceous material found in retained samples.
Product
AMINOSYN II 15% An Amino Acid Injection, Sulfite-Free, 2000 mL in flexible containers, Rx ONLY, Hospira, Inc., Lake Forest, IL 60045. NDC 0409-7171-17
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1005-2021·2021-09-22
Loki Fish Wild Keta Salmon Lox Recalled for Listeria Contamination
Loki Fish Company is recalling Loki Fish Wild Keta Salmon Lox (4 oz. pouches, UPC 92103 00111) distributed in Oregon and Washington due to potential Listeria monocytogenes contamination.
Product
Loki Fish Wild Keta Salmon Lox, packaged in a 4 oz. plastic pouch, sliced on a coated board, 24 packages to a case. UPC 92103 00111. The label is read in parts: LOKI FISH *** WILD KETA LOX *** Ingredients: Wild Keta salmon, honey, salt and spices *** PRODUCT OF USA *** KEEP RE
Category
Food
Distribution
0 states
CriticalFDA (Devices)·Z-2402-2021·2021-09-15
Pipeline Flex Embolization Device Recalled for Potential Push Wire Fracture Risk
Micro Therapeutics recalls Pipeline Flex Embolization Devices for potential push wire fractures in the delivery system during use. Device fractures in the Hypotube may result in malfunction during vascular procedures.
Product
Pipeline Flex Embolization Device
Category
Medical Device
Distribution
48 states
CriticalFDA (Devices)·Z-2392-2021·2021-09-15
Eco-Med ultrasound gels and lotions recalled for bacterial contamination
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. are being recalled due to potential bacterial contamination. The FDA issued a Class I recall on August 18, 2021, advising health care providers to stop using all affected products.
Product
LiquaSonic Ultrasound Gel 5L, Model No. 001222
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2391-2021·2021-09-15
FDA Recalls Ultrasound Gel for Risk of Bacterial Contamination
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. are being recalled due to the risk of bacterial contamination. Healthcare providers and consumers should stop using affected products.
Product
LiquaSonic Ultrasound Gel 250mL, Model No. 001205
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2403-2021·2021-09-15
EV3 Pipeline Flex Embolization Device Recalled for Push Wire Fracture Risk
Micro Therapeutics Inc. is recalling 16,169 EV3 Pipeline Flex Embolization Devices due to potential push wire fractures in the delivery system during use.
Product
EV3 Pipeline Flex Embolization Device with Flex Shield Technology
Category
Medical Device
Distribution
48 states
SevereFDA (Devices)·Z-2377-2021·2021-09-15
NORMOFLO Irrigation Warming Sets Recalled for Aluminum Leaching Risk
Smiths Medical is recalling NORMOFLO Irrigation Warming sets (Models IR-40, IR-500, IR-600, IRI-600, IRI-600B, IR-700) due to potential aluminum leaching when used at lower flow rates with certain solutions and blood products. No illnesses have been reported.
Product
NORMOFLO Irrigation Warming administration set (disposable), Models IR-40, IR-500, IR-600, IRI-600, IRI-600B, IR-700
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2376-2021·2021-09-15
NORMOFLO Irrigation Fluid Warmer Recalled for Risk of Aluminum Leaching
Smiths Medical recalls NORMOFLO Irrigation Fluid Warmer Models H-1100 and H-1129 (913 units) due to potential harmful aluminum leaching when used at lower flow rates with certain solutions and blood products.
Product
NORMOFLO Irrigation Fluid Warmer Models H-1100 and H-1129
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·21V706000·2021-09-10
2022 Nissan Pathfinder Hood Latch Bracket May Detach, Posing Crash Risk
Nissan is recalling 2022 Pathfinder vehicles due to insufficient welds on the secondary hood latch bracket. The bracket may detach, allowing the hood to open if the primary latch fails, obstructing the driver's view and increasing crash risk.
Product
NISSAN — 2022 NISSAN PATHFINDER
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·21780·2021-09-09
Teak shower benches recalled due to fall hazard and collapse risk
Ivena teak shower benches sold at Costco can collapse during use, posing a fall hazard. Consumers have reported 81 incidents of collapse or breakage, including four injuries.
Product
Teak shower benches
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0778-2021·2021-09-08
Hand Sanitizer Gel Recalled Due to Methanol Contamination Risk
Global Sanitizers LLC is recalling MEDICALLY MINDED ANTIMICROBIAL Hand Sanitizer Gel (70% ethyl alcohol) due to manufacturing deviations. Products were made under the same conditions as a lot found to contain methanol.
Product
MEDICALLY MINDED ANTIMICROBIAL Hand Sanitizer Gel with Aloe Vera, (Ethyl Alcohol 70% v/v), 10 FL OZ / 300 mL, Manufactured by Grupo V-Klean S.A. de C.V, Calle Alborada 124, Parques del Pedregal, Tlalpan, 14250 Ciudad de Mexico, CDMX, Distributed by SBL Brands, LLC. Las Vegas, NV
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0888-2021·2021-09-08
BrightFarms Sunny Crunch Lettuce Recalled for Salmonella Risk
Bright Farms is recalling BrightFarms Sunny Crunch lettuce sold in 4oz and 8oz plastic clamshells because the product may be contaminated with Salmonella.
Product
BrightFarms Sunny Crunch; packaged in clear, plastic clamshells; 4oz and 8oz; grown at the company's Rochelle, Illinois indoor farm
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0891-2021·2021-09-08
BrightFarms 50/50 Spring & Spinach Salmonella Contamination Recall
BrightFarms 50/50 Spring & Spinach in 4oz clamshells may be contaminated with Salmonella. The product was distributed in Illinois, Wisconsin, Iowa, Indiana, and Michigan with best-by dates through July 29, 2021.
Product
BrightFarms 50/50 Spring & Spinach; packaged in clear plastic clamshells, 4oz; grown at the company's Rochelle, Illinois indoor farm
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0902-2021·2021-09-08
Cahill Whiskey Cheddar Cheese Recalled for Potential Listeria Contamination
Whole Foods Market is recalling Cahill Whiskey Cheddar Cheese due to potential contamination with Listeria monocytogenes. The cheese was distributed to stores across multiple states from May to July 2021.
Product
Cahill Whiskey Cheddar Cheese packaged in clear plastic PLU 5478494884
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0894-2021·2021-09-08
BrightFarms Butter Crisp Lettuce Recalled for Salmonella Risk
BrightFarms Butter Crisp lettuce packaged in 4-oz clear plastic clamshells is being recalled due to potential Salmonella contamination. The product was distributed in Illinois, Wisconsin, Iowa, Indiana, and Michigan with best-by dates through July 29, 2021.
Product
BrightFarms Butter Crisp; packaged in clear, plastic clamshells; 4oz; grown at the company's Rochelle, Illinois indoor farm
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0893-2021·2021-09-08
BrightFarms Spring Crunch Lettuce Recall Due to Salmonella Risk
BrightFarms Spring Crunch lettuce packaged in 4oz clear plastic clamshells may be contaminated with Salmonella. The recall affects products distributed in Illinois, Wisconsin, Iowa, Indiana, and Michigan with best-by dates through July 29, 2021.
Product
BrightFarms Spring Crunch; packaged in clear, plastic clamshells; 4oz; grown at the company's Rochelle, Illinois indoor farm
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0901-2021·2021-09-08
Cahill Cheddar with Porter Cheese Recalled for Listeria Contamination Risk
Whole Foods Market is recalling Cahill Cheddar with Porter cheese (PLU 93579) sold in clear plastic packaging due to potential contamination with Listeria monocytogenes, a serious foodborne pathogen.
Product
Cahill Cheddar with Porter PLU 93579 packaged in clear plastic
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0890-2021·2021-09-08
BrightFarms Harvest Crunch Salmonella Contamination Recall
BrightFarms Harvest Crunch packaged salad may be contaminated with Salmonella. The recall affects products distributed in Illinois, Wisconsin, Iowa, Indiana, and Michigan with best-by dates through July 29, 2021.
Product
BrightFarms Harvest Crunch; packaged in clear plastic clamshells; 4oz; grown at the company's Rochelle, Illinois indoor farm
Category
Food
Distribution
5 states
SevereNHTSA·21V697000·2021-09-08
2021 Porsche Taycan: Brake booster defect may cause brake pedal failure
Certain 2021 Porsche Taycan vehicles have a loose pressure input rod connection on the brake booster that may detach, causing brake pedal failure and increasing crash risk. Dealers will repair or replace the brake booster free of charge.
Product
PORSCHE — 2021 PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0782-2021·2021-09-08
MEDICALLY MINDED Hand Sanitizer Gel Recalled for Methanol Contamination
Global Sanitizers LLC is recalling MEDICALLY MINDED Hand Sanitizer Gel (Ethyl Alcohol 70% v/v, 8.5 FL OZ / 250 mL) distributed nationwide due to manufacturing conditions that led to methanol contamination in product lots.
Product
MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8.5 FL OZ / 250 mL bottle, Made in Mexico, Distributed by SBL Brands, LLC Las Vegas, NV 89119. UPC: 6 76753 00359 1 ,
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0895-2021·2021-09-08
BrightFarms Nutrigreens Recalled for Potential Salmonella Contamination
BrightFarms Nutrigreens 3oz packages may be contaminated with Salmonella. The product was grown at the company's Rochelle, Illinois indoor farm and distributed across Illinois, Wisconsin, Iowa, Indiana, and Michigan with best-by dates through July 29, 2021.
Product
BrightFarms Nutrigreens; packaged in clear, plastic clamshells; 3oz; grown at the company's Rochelle, Illinois indoor farm
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0889-2021·2021-09-08
BrightFarms Spring Mix Recalled Due to Salmonella Risk
BrightFarms Spring Mix sold in 4oz and 8oz clamshells may be contaminated with Salmonella. The product was distributed across Illinois, Wisconsin, Iowa, Indiana, and Michigan with best-by dates through July 29, 2021.
Product
BrightFarms Spring Mix; packaged in clear, plastic clamshells; 4oz and 8oz; grown at the company's Rochelle, Illinois indoor farm
Category
Food
Distribution
5 states

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7151–7175 of 7514