Archive
1,013 recalls were announced in March 2023.
Of the 1,013 recalls this month scored against our rubric, 7% are Critical, 44% are Severe.
Which agencies issued them
Accord Healthcare is recalling rosuvastatin 40 mg tablets distributed in the US, Puerto Rico, and Canada due to manufacturing quality control deviations found during an FDA inspection. No illnesses have been reported.
Accord Healthcare is recalling Atorvastatin Calcium 10 mg tablets distributed in the United States, Puerto Rico, and Canada following FDA inspection findings of manufacturing deviations.
Accord Healthcare is recalling Glimepiride 4 mg tablets due to Current Good Manufacturing Practice deviations discovered during an FDA inspection. Approximately 1.16 million bottles across the United States, Puerto Rico, and Canada are affected.
Accord Healthcare is recalling 8,184 bottles of Ropinirole 4 mg tablets due to manufacturing practice deviations found during an FDA inspection. The recalled batches were distributed in the United States, Puerto Rico, and Canada.
Corim Industries is recalling Agglomerated Peanut Butter Hot Chocolate and Peanut Butter Cappuccino products in multiple formats due to undeclared peanut allergen on the label.
Accord Healthcare is recalling Pirfenidone 801 mg tablets due to Current Good Manufacturing Practice deviations identified during an FDA inspection. Affected batches P2202519 and P2202513 were distributed in the United States, Puerto Rico, and Canada.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Off Grid Trailers is recalling 150 Expedition, Switchback, and Pando travel trailers because a cooktop component may fracture and cause a gas leak.
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.
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.
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.
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.
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.
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.
Continental Tire is recalling specific General Altimax RT43 tires because they lack required identification markings, which could hinder future recall efforts.
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.
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.
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 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.
Draeger Medical recalls NovaStar TS Anti-Asphyxia Valves due to magnets that may interfere with implanted and non-implanted medical devices and metallic implants.
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 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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
Forest River is recalling 2013 Coachmen Cross Country and 2023 Coachmen Sportscoach motorhomes because the entry door latch may fail, preventing entry or exit.
Daiso California Warehouse is recalling Tohato Caramel Corn 5-packs because almond appears in the ingredient list but is missing from the allergen Contains statement. Consumers with almond allergies who rely on the allergen statement may unknowingly consume this product.
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.
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.
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.
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.
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.
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.
Tampico Spice Company is recalling Cajun Seasoning in multiple sizes due to elevated aflatoxin contamination. Affected lots were distributed across eight states.
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.
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.
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.
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.
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 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).
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. voluntarily recalled specific lots of TIROSINT (levothyroxine sodium) Oral Solution nationwide due to subpotency. The affected medication contains less active ingredient than labeled.
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 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.
B. Braun Medical is recalling 0.9% Sodium Chloride Injection due to possible incomplete container seals that may leak. The recall involves 483,229 bags distributed nationwide.
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).
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 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.
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.
Medline Industries recalls approximately 720 Sterile Maximum Barrier Pack-LF units due to improper component placement preventing sterilization. The affected packs were distributed in Arkansas, Colorado, and Georgia.
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.
IBSA Pharma is recalling TIROSINT levothyroxine sodium oral solution nationwide due to subpotent drug content. The recall affects lots 220413 and 220964.
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.
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.
Hologic is recalling 797 units of its 3Dimensions/Selenia Dimensions mammography systems nationwide due to unexpected C-arm movement that may cause blunt trauma.
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.
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.
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.
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. recalls TIROSINT (levothyroxine sodium) oral solution nationwide due to subpotent formulation containing less active ingredient than labeled.
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).
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.
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 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.
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.
B. Braun Medical's 0.9% Sodium Chloride Injection batches recalled due to risk of incomplete seals that could allow leakage, potentially compromising sterility. The recall affects 1,343,982 bags distributed nationwide.
Access Vascular is recalling the HydroMID 4Fr Single Lumen Maximal Barrier Kit because the outer bag and inner Tyvek header bag are mislabeled. The device is used for short-term peripheral venous access.
Looking for a different month? Back to 2023.