Archive
1,013 recalls were announced in March 2023.
Of the 1,013 recalls this month scored against our rubric, 7% are Critical, 43% are Severe.
Which agencies issued them
Accord Healthcare is recalling Buspirone Hydrochloride tablets due to manufacturing process deviations found during an FDA inspection. The recall affects approximately 3,784 bottles distributed in the United States, Puerto Rico, and Canada.
Accord Healthcare is recalling Simvastatin 10 mg tablets distributed in the U.S., Puerto Rico, and Canada due to manufacturing process deviations discovered during FDA inspection. Patients should contact their pharmacy or healthcare provider.
Sciegen Pharmaceuticals is recalling 4,392 bottles of Gabapentin 600 mg tablets after a pharmacist discovered some 800 mg tablets mixed into bottles.
Accord Healthcare is recalling 44,068 bottles of Doxazosin 1 mg tablets distributed in the US, Puerto Rico, and Canada due to Current Good Manufacturing Practice deviations found during an FDA inspection.
DuPont Nutrition USA is recalling BD-102 NF Microcrystalline Cellulose, a pharmaceutical excipient, due to failed conductivity specifications. Affected batches were distributed nationwide and internationally for use in drug manufacturing.
Accord Healthcare is recalling Pravastatin Sodium 10 mg tablets for CGMP deviations found during FDA inspection. About 9,600 bottles were distributed across the United States, Puerto Rico, and Canada. No illnesses reported.
Accord Healthcare recalls approximately 665,469 bottles of Montelukast Sodium 10 mg tablets due to manufacturing process deviations discovered during FDA inspection.
DuPont is recalling Avicel PH-200, a pharmaceutical excipient, because test results showed conductivity out of specification. No illnesses or injuries have been reported.
SAF-Holland is recalling ADZ-123-9 truck suspensions because the rear lower control arm may fail, potentially causing loss of vehicle control.
Terex Advance is recalling 2022 Front Discharge Mixer Commander vehicles because front-drive steer axle fasteners may not be tightened sufficiently, risking axle separation and loss of control.
Grand Design is recalling 139 units of 2023 Imagine travel trailers. The Federal Certification Label incorrectly states tire size and inflation pressure, which may cause premature tire wear or blowout, increasing crash risk.
Kia is recalling 2021-2023 K5 vehicles due to potentially incorrect installation of side curtain air bags that could prevent proper deployment in a crash.
Newell Coach Corp. is recalling 2023-2024 P50 motor coaches because brake lights may fail to illuminate unless the brake pedal is fully depressed, increasing crash risk.
Dahlia Imports is recalling approximately 196,019 pounds of raw bone-in goat products imported from Australia without the required USDA import reinspection.
Triumph is recalling certain 2023 Bonneville T120 motorcycles because the left-hand side brake disc may detach, reducing brake performance and increasing crash risk. Dealers will install replacement parts free of charge.
GH Foods NW, LLC is recalling approximately 106 pounds of Trader Joe's Lemon Chicken & Arugula Salad because the label fails to declare wheat, a known allergen.
Dorel Juvenile Group is recalling specific Safety 1st and Maxi-Cosi child seats because lower anchors may fail, allowing the seat to detach in a crash.
Forest River is recalling 2020-2023 Palomino Solaire 320TSBH travel trailers because missing freshwater tank supports may cause the tank to dislodge and fall, creating a road hazard.
Xos is recalling 275 RM01, SA01, and SV05 vehicles because improperly tightened bolts may allow the driveshaft to separate, increasing crash risk.
Lordstown is recalling 2023 Endurance vehicles because worn electric park brake washers may cause the vehicle to roll away.
Toyota is recalling 2022-2023 Tundra and Tundra Hybrid trucks with Toyota genuine tonneau covers. The cover's attachment joints may loosen and allow the cover to detach while driving, creating a road hazard.
Harbor Freight is recalling Central Hydraulics High Position Motorcycle Lifts because welds or tubing may break, causing the lift to fall or drop the motorcycle.
Mack is recalling approximately 17 model-year 2023 Granite trucks because front-drive steer axle fasteners may not have been properly tightened and could come loose, risking loss of steering control and crashes.
Jaguar Land Rover is recalling 2023 Defender 130 vehicles with third-row seats because the seatback latch may not secure child seat tethers properly, increasing crash injury risk.
Ouwoer Kids Bike Helmets sold on Amazon from March to November 2022 fail to meet federal safety standards and may not protect children in a crash. About 120 units are affected; no injuries have been reported.
The TJX Companies is recalling approximately 81,700 office chairs because the back can break or detach from the seat base when occupied, posing a fall hazard. The firm has received 12 reports of the chair back failing, including 10 reports of injuries.
Newmar is recalling certain 2021-2023 Bay Star, Bay Star Sport, and Canyon Star motorhomes because the entry door latch may fail and prevent entry or exit, increasing the risk of injury in emergencies.
Helly Hansen is recalling about 13,900 adult workwear sweatshirts and hoodies because they fail to meet federal flammability standards for clothing textiles, posing a risk of burn injuries.
Primark is recalling about 1,665 children's bamboo plates sold from October 2021 through August 2022 because they contain elevated levels of lead and formaldehyde, which are toxic if ingested by children.
Smocked Runway is recalling about 7,200 Classic Whimsy children's pajamas that fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries. Consumers should stop using the product immediately and contact the manufacturer for return instructions.
Off Grid Trailers is recalling 150 Expedition, Switchback, and Pando travel trailers because a cooktop component may fracture and cause a gas leak.
Winnebago is recalling certain 2023 Adventurer, Vista, and Itasca Sunstar motorhomes for missing rear reflectors that fail federal safety standards. Missing reflectors reduce visibility to other drivers, increasing crash risk.
Patagonia is recalling about 8,000 Infant Capilene Midweight Base Layer Sets because snaps on the bodysuit can detach, posing a choking hazard to infants. One incident of a snap detaching and being mouthed by a baby has been reported.
RELiON Battery is recalling certain lots of InSight Series 48V lithium-ion batteries because they can overheat, posing thermal burn and fire hazards. The company has received five reports of overheating with no injuries reported to date.
DR Power is recalling about 2,100 PRO XL501 Chipper Shredders because the fin scroll can fail and eject metal pieces from the hopper during operation. No injuries have been reported, but the company has received six reports of metal ejection.
Active Sports is recalling CTRL Imperial Wakeboard Bindings because the binding can partially detach from the baseplate or the external mount can crack, causing users to lose balance and fall into the water. The company has received 21 reports of detachment or cracking but no injuries have been reported.
Continental Tire is recalling specific General Altimax RT43 tires because they lack required identification markings, which could hinder future recall efforts.
Daiso is recalling Harvest Sesame 94g units due to undeclared soy and sesame allergens on the label. The recall affects 317,751 units distributed across Daiso retail locations in six U.S. states and Canada.
Daiso is recalling KASHIWADO Hitoritoiro Fly Beans Senbei because the product contains peanuts not listed on the label, creating a risk for consumers with peanut allergies.
Harvest Biscuits 4Kinds of Nuts (94g units) are recalled because the product contains soy and peanuts that are not listed on the ingredient label. The product was distributed to Daiso stores across multiple US states and Canada.
Rao's Made for Home Slow Simmered Soup labeled as Chicken & Gnocchi is being recalled because it actually contains vegetable minestrone with an undeclared egg allergen. The recall affects 13,751 cases distributed across multiple states.
Daiso California Warehouse is recalling Katoseika Chocolat Orange Candy (60g) due to undeclared soy allergen. The product was distributed to Daiso stores across multiple U.S. states and Canada.
DAISO CALIFORNIA WAREHOUSE is recalling MEITO Powdered Apple Tea 4packs because the product contains milk that is not declared on the label. Consumers with milk allergies should not consume this product.
Caramel Corn Boys Festival snack packs, distributed to Daiso stores, contain undeclared almonds and peanuts. This creates serious health risks for consumers with nut allergies.
Draeger Medical is recalling 893 units of NovaStar TS Standard elbow components due to magnets that could interfere with medical devices and metallic implants.
Pilgrim's Roasted Nut'Z Squirrel Mix (8 oz bags) is recalled for undeclared milk, soy lecithin, and food colors. The product poses allergic reaction risk to consumers with milk or soy allergies.
DAISO CALIFORNIA WAREHOUSE is recalling ITOSEIKA Chocolate Chip Cookies due to undeclared milk allergen on the label. Products were distributed to Daiso stores in California, Washington, Nevada, Texas, New York, New Jersey, and British Columbia.
KASHIWADO Hitoritoiro Fly Beans Senbei crackers are being recalled because the product contains peanuts that are not listed on the ingredient label. Consumers with peanut allergies should avoid this product.
Draeger Medical recalls NovaStar TS Anti-Asphyxia Valves due to magnets that may interfere with implanted and non-implanted medical devices and metallic implants.
Pilgrim's Roasted Nut'Z Chocolate Toffee Almonds are recalled due to undeclared milk and soy lecithin. The product poses a serious risk to consumers with dairy and soy allergies.
Daiso potato crackers with sardines (46g) are being recalled due to undeclared milk allergen. The product was distributed across six US states and parts of Canada.
Pilgrim's Roasted Nut'Z English Toffee Peanuts (580 packages) are recalled because the label does not declare the presence of milk. Consumers with milk allergies should not consume this product.
TOHATO Bitter Caramel Corn 77g units are recalled because they contain almonds not listed on the ingredient label. This poses a serious risk to consumers with almond allergies.
TOHATO Nagewa Snack Seaweed Flavor contains undisclosed milk and shellfish allergens. The product is distributed to Daiso stores in CA, WA, Nevada, TX, NY, and NJ; consumers with these allergies should not consume.
Caramel Corn The Star Festival 80g units are recalled because they contain almonds that are not listed on the ingredient label. About 317,751 units were distributed to Daiso stores in six U.S. states and Canada.
KANRO Pure gummy candies are being recalled due to undeclared soy allergen on the label. The recall affects 113,205 units sold at Daiso stores across multiple states and Canada.
TOHATO Caramel Corn products sold at Daiso stores are being recalled because almonds are present but not listed on the ingredient label, posing risk to people with almond allergies.
Medline Sterile Hand Pack surgical prep kits are recalled because components were improperly placed in the nonsterile portion of the tray and did not receive proper sterilization. Affects 1,689 trays distributed in AR, CO, and GA.
Cardinal Health's Presource Packs IV START KIT is being recalled due to a manufacturing defect in the connector that may cause fluid leaks and compromise intravenous fluid delivery.
BAKE'N JOY FOODS is recalling Gordon Choice Cranberry Orange Flavored Nut muffin batter due to undeclared soy lecithin. Consumers with soy allergies face a reaction risk.
IBSA Pharma is recalling certain lots of TIROSINT (levothyroxine sodium) oral solution nationwide because the product contains less active ingredient than labeled. Patients using affected lots may not receive adequate thyroid hormone replacement.
Siemens is recalling the Atellica IM Folate 140 test kit due to negative bias that occurs when whole blood calibration is mistakenly used to test serum samples, potentially producing falsely low folate measurements.
TIROSINT (levothyroxine sodium) oral solution has been recalled nationwide by IBSA Pharma Inc. due to subpotency, with the affected medication containing less active ingredient than labeled.
Siemens Luminos dRF Max diagnostic imaging systems are being recalled due to a risk of collision with ceiling, walls, or nearby objects caused by default room configuration settings. This could result in serious injury to staff or patients.
Siemens is recalling ADVIA Centaur diagnostic test kits used to detect hepatitis B antibodies due to test interference that can produce false positive results when performed before another hepatitis B test on the same sample.
Siemens Healthcare Diagnostics is recalling 7,884 ADVIA Centaur Folate 500 diagnostic test kits because using whole blood calibration with serum samples produces negative bias and inaccurate results.
Access Vascular is recalling HydroMID 4Fr Single Lumen Maximal Barrier Kits due to an incorrect component listed on the inner kit label. The error could lead to confusion and improper use of the device.
Pilgrim's Roasted Nut'Z White Chocolate Raspberry Cashews are recalled due to undeclared milk and soy lecithin. The product was distributed in California, Oregon, and Washington.
Cardinal Health Presource Packs IV start kits with ICU MicroClave Clear Connectors are being recalled due to a manufacturing defect that may cause fluid leaks and loss of fluid path integrity.
Siemens Healthcare is recalling 1,865 Atellica IM Folate 700 diagnostic kits nationwide and internationally. The kits may produce inaccurate folate test results when whole blood calibration is used instead of serum calibration.
Siemens Uroskop Omnia Max imaging systems are recalled due to collision risk with ceilings, walls, or objects caused by default configuration settings. The systems may move dangerously, potentially injuring staff or patients.
Pilgrim's Roasted Nut'Z Creme Brulee Cashews are recalled for undeclared walnut. The product was distributed in California, Oregon, and Washington and poses a risk to consumers with walnut allergies.
IBSA Pharma Inc. recalled TIROSINT levothyroxine sodium lot 220853 nationwide due to subpotency. The oral solution may contain less active ingredient than labeled, potentially affecting thyroid hormone replacement therapy.
Airstream is recalling 2021-2023 travel trailers with SDS2 cooktops. Burner tubes may fracture and cause gas leaks, increasing fire risk. Dealers will install a support bracket at no charge.
IBSA Pharma Inc. is recalling TIROSINT (levothyroxine sodium) oral solution nationwide due to subpotency. Two lot numbers are affected: Lot #220407 (Exp. 10/2023) and Lot #220960 (Exp. 03/2024).
IBSA Pharma has recalled TIROSINT levothyroxine sodium oral solution nationwide due to subpotency. Affected lots 220418 and 220560 may contain insufficient active ingredient for proper thyroid hormone replacement therapy.
Certain 2023 Mazda CX-50 vehicles with a trailer hitch may have a harness that detaches and becomes damaged, causing trailer lights and brakes to fail. This increases the risk of crashes when towing.
Siemens ADVIA Centaur Folate 100 test kits are recalled due to negative bias when whole blood calibration is used to test serum samples. The affected kits may produce falsely low folate results.
IBSA PHARMA is recalling TIROSINT (levothyroxine sodium) oral solution due to subpotency in specific batches. The affected product may contain less active ingredient than labeled.
IBSA Pharma has recalled two lots of TIROSINT levothyroxine sodium oral solution nationwide because they contain less active ingredient than labeled. The affected lots are 220409 (expiring 10/2023) and 220956 (expiring 03/2024).
IBSA Pharma Inc. voluntarily recalled specific lots of TIROSINT (levothyroxine sodium) Oral Solution nationwide due to subpotency. The affected medication contains less active ingredient than labeled.
IBSA Pharma voluntarily recalled TIROSINT levothyroxine sodium oral solution nationwide due to subpotency concerns. Affected lots are 220416 (Exp. 10/2023) and 221053 (Exp. 4/2024).
Tampico Spice Company is recalling Taco Meat Seasoning due to elevated aflatoxin levels. Affected products in multiple sizes were distributed across eight states.
Cardinal Health is recalling Presource Packs IV START TRAY I kits due to a manufacturing defect in the ICU MicroClave Clear Connector that may cause fluid leaks and loss of fluid path integrity.
Siemens Luminos Agile Max diagnostic imaging systems recalled due to default configuration parameters allowing collision with room structures, risking serious injury to staff or patients.
IBSA Pharma Inc. has recalled TIROSINT levothyroxine sodium oral solution nationwide due to subpotency. Some doses may contain less active ingredient than labeled. Patients should contact their healthcare provider.
Siemens recalls Luminos Agile imaging systems that may collide with ceilings or walls due to default configuration settings, potentially causing serious injury to staff or patients.
Pilgrim's Roasted Nut'Z Tri-Colored Chocolate Espresso Beans are recalled due to undeclared soy lecithin. Consumers with soy allergies may experience allergic reactions.
Siemens Luminos dRF diagnostic imaging system is being recalled nationwide due to potential collision with ceilings, walls, or objects caused by default room configuration parameters. Collisions could result in serious injury to patients or staff.
Ferrari is recalling 2021-2023 SF90 Stradale and 2022 SF90 Spider vehicles because the passenger air bag may impact a child seat, increasing injury risk.
Siemens is recalling ADVIA Centaur Folate 500 test kits because a calibration error causes inaccurate, falsely low results when testing serum samples, potentially affecting diagnostic accuracy.
Dr. Reddy's Laboratories is recalling Tacrolimus 0.5 mg capsules due to the presence of one 1 mg capsule co-mingled in affected bottles. The mismatched capsule could lead to incorrect dosing in immunosuppressed patients.
Medline is recalling sterile oncology port access trays in which some components were not properly sterilized due to improper placement during manufacturing. Healthcare facilities should immediately discontinue use of affected units.
Siemens Healthcare is recalling 9,272 Atellica IM Folate 700 test kits due to negative bias in results when whole blood calibration is used to test serum samples.
Nature's Eats Cashew Crave Mix 8 oz. is recalled for undeclared milk and soy allergens. The allergens are present in the product but not declared in the main 'Contains' statement.
Forest River is recalling 2013 Coachmen Cross Country and 2023 Coachmen Sportscoach motorhomes because the entry door latch may fail, preventing entry or exit.
Pilgrim's Roasted Nut'Z Garlic, Parmesan, Cracked Black Pepper Hazelnuts are recalled due to undeclared milk, a major allergen.
Tampico Spice Company Inc is recalling Cayenne Pepper in 1-pound and 5-pound jars due to elevated aflatoxin levels. The affected lot is #2112245, distributed across eight states.
Rising Pharmaceuticals is recalling Warfarin Sodium Tablets USP 1 mg due to failed impurities and degradation specifications. Approximately 12,216 bottles may have been distributed nationwide.
IBSA Pharma Inc. recalls TIROSINT (levothyroxine sodium) oral solution nationwide due to subpotent formulation containing less active ingredient than labeled.
Looking for a different month? Back to 2023.