Safety Recalls
RSS ↗17,559 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 3,451–3,500 of 17,559
- Class II
Food Recall · February 21, 2026
CLOVER SONOMA SOUR CREAM NET WT 8OZ UPC 0 70852 61800 5 & 16OZ UPC 0 70852 61500 4 DISTRIBUTED BY: CLOVER-STORNETTA FARMS LLC PETALUMA, CA 94952Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- Class II
Food Recall · February 21, 2026
Great Value Lowfat Cottage Cheese Small Curd 2% Milkfat NET WT 24OZ UPC 0 78742 11673 0 DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- Class II
Food Recall · February 21, 2026
Great Value Fat Free Cottage Cheese Small Curd 0% Milkfat NET WT 24OZ UPC 0 78742 37339 3 DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- Class II
Food Recall · February 21, 2026
CLOVER SONOMA COTTAGE CHEESE LOW FAT 2% MILKFAT NET WT 16OZ UPC 0 70852 54400 7 & 32OZ UPC 0 70852 54200 3 DISTRIBUTED BY: CLOVER-STORNETTA FARMS LLC PETALUMA, CA 94952Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- Class II
Food Recall · February 21, 2026
Great Value Cottage Cheese Small Curd 4% Milkfat NET WT 16oZ UPC 0 78742 37235 8; 24oz UPC 0 78742 37236 5 & 3lb UPC 0 78742 14797 0 DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- Unclassified
Vehicle Recall · February 20, 2026
2023 FORD EXPEDITION, 2023 FORD MAVERICK, 2023 FORD F-550 SD, 2023 FORD F-450 SD, 2023 FORD F-600 SD, 2023 LINCOLN NAVIGATOR, 2024 FORD EXPEDITION, 2024 FORD MAVERICK, 2024 FORD F-450 SD, 2024 FORD F-Trailer lights or brakes that do not function can reduce the driver’s ability to control the trailer and decrease the trailers visibility to other road users, increasing the risk of a crash.
- Unclassified
Vehicle Recall · February 20, 2026
2025 VOLVO EX30A high voltage battery that overheats increases the risk of a fire.
- Class II
Medical Device Recall · February 20, 2026
Brand Name: Elegance¿ Anterior Cervical Plate Product Name: ELEGANCE 1 LEVEL CERVICAL PLATE, ELEGANCE 2 LEVEL CERVICAL PLATE, ELEGANCE 3 LEVEL CERVICAL PLATE, ELEGANCE 4 LEVEL CERVICAL PLATE Model/CDue to a quality issue regarding the presence of burr on the finished cervical plate product.
- Class II
Medical Device Recall · February 20, 2026
Radius VSM Disposable NIBP Cuff, REF: 4825, 4826Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate patients, which may distract clinicians away from management of true positive alarms, which could delay treatment; 2) Small and medium size blood pressure cuffs may contain rough edges, may result in skin irritation/redness.
- Class II
Medical Device Recall · February 20, 2026
Radius VSM ECG pre-connected Set, REF: 4842, 4695Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate patients, which may distract clinicians away from management of true positive alarms, which could delay treatment; 2) Small and medium size blood pressure cuffs may contain rough edges, may result in skin irritation/redness.
- Unclassified
Consumer Product Recall · February 19, 2026
Shenzhen Huakechuang Technology Co. Ltd., dba Huaker, of China
Huaker Magnetic Balls and Rods SetsThe recalled magnet toy building sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard.
- Unclassified
Consumer Product Recall · February 19, 2026
Shenzhen Yimu Technology Co., Ltd. dba JJGoo, of China
JJGoo LED Balloon LightsThe recalled lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings required by Reese's Law. When button cell batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- Unclassified
Consumer Product Recall · February 19, 2026
Ningbo Shenyu Medical Equipment Co., Ltd., of China
Vive Health Bed RailsThe recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Sundried Tomato Cream Cheese; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Class II
Medical Device Recall · February 19, 2026
AMO Puerto Rico Manufacturing, Inc.
Brand Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Product Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Model/Catalog Number: DIB00 Software Version: N/A PrDue to identifying a limited quantity of intraocular lenses that may have a haptic that sticks to the optic which prevents the lens from unfolding as consistently as expected.
- Unclassified
Vehicle Recall · February 19, 2026
Jaguar Land Rover North America, LLC
2023 LAND ROVER RANGE ROVER, 2023 LAND ROVER RANGE ROVER SPORT, 2024 LAND ROVER RANGE ROVER, 2024 LAND ROVER RANGE ROVER SPORTA detached panoramic sunroof side trim can become a road hazard, increasing the risk of injury or crash.
- Class III
Food Recall · February 19, 2026
MEI HEONG YUEN GARLIC FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts, Salt, Garlic, Liquorice, Sugar, Saccharin; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd;Products contain cyclamates (banned sweetener)
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Strawberry Cream Cheese; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Apple Cinnamon Cream Cheese; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Lox Cream Cheese; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Scallion Cream Cheese; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Blueberry Cream Cheese; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Class III
Food Recall · February 19, 2026
MEI HEONG YUEN WALNUT FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts, Salt, Liquorice, Sugar, Spices, Sodium Cyclamate, Acesulfame-K, Vanilla, Ethyl Maltol; Shelf Life: 18 Months; ManufaProducts contain cyclamates (banned sweetener)
- Class III
Drug Recall · February 19, 2026
Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphate Capsules 300 mg, International Isotopes Inc., Idaho Falls, ID 83401. NDC: 692Failed Tablet/Capsule Specifications
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Tofu Whipped; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Unclassified
Consumer Product Recall · February 19, 2026
SAMIT Youth Multi-Purpose HelmetsThe recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the positional stability and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.
- Class II
Food Recall · February 19, 2026
Willamette Valley Pie Company, LLC
Frozen Raw Bulk 8 inch Blueberry Crumble Pie (4 pies/case). Net wt. 24.5oz. UPC 0002251881223. Handmade - Willamette Valley Pie Company LLC. 1651 Eska Way, Silverton, OR. Frozen Raw pies were sold frPotential contamination with listeria monocytogenes.
- Class II
Food Recall · February 19, 2026
Willamette Valley Pie Company, LLC
Frozen Raw Bulk 9 inch Blueberry Crumble Pie ES (4 pies/case). Net wt. 38oz. UPC 00022518893257. Handmade - Willamette Valley Pie Company LLC. 1651 Eska Way, Silverton, OR. Frozen raw pies were soldPotential contamination with listeria monocytogenes.
- Unclassified
Consumer Product Recall · February 19, 2026
Meijer Distribution, Inc., of Grand Rapids, Michigan
Meijer one-piece footed 12-, 18-and 24-month children's sleepwearThe recalled sleepwear violates the mandatory flammability standard for children's sleepwear, posing a risk of burn injuries to children.
- Unclassified
Consumer Product Recall · February 19, 2026
Prismatic 3D Prints LLC of Loveland, Colorado
Prismatic 3D Prints Book Nooks with LightsThe recalled book nooks violate the mandatory standard for consumer products containing button cell or coin batteries because the nooks include a spare lithium coin battery that can be easily accessed by children. In addition, the spare coin battery is not in child resistant packaging, and the packaging does not have the warnings as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Whipped Cream Cheese; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Jalapeno Cream Cheese; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Unclassified
Consumer Product Recall · February 19, 2026
Joly's LLC, of Orlando, Florida
Joly's 80% Vinegar (32 oz, pack of two)The recalled vinegar product violates the precautionary labeling requirements under the Federal Hazardous Substances Act (FHSA) because the hazardous substance lacks required warning labels and first-aid treatment instructions. This poses a deadly risk of poisoning if the contents are swallowed and a serious injury from chemical burns to the skin and eyes if improperly handled.
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Vegetable Cream Cheese; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Garlic & Herb Cream Cheese; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Walnut Raisin Cream Cheese; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Jalapeno Cheddar Cream Cheese; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Class III
Food Recall · February 19, 2026
MEI HEONG YUEN TANGERINE FLAVOR ROASTED PEANUTS; NET 9.17 oz (260g); Ingredients: Peanuts, Salt, Sugar, Liquorice, Spices, Sodium Cyclamate, Acesulfame-K, Vanilla, Ethyl Maltol; Shelf Life: 18 Months;Products contain cyclamates (banned sweetener)
- Class I
Food Recall · February 19, 2026
Made Fresh Salads brand Caramel Apple Cream Cheese; 5 lb white plastic tubProducts may be contaminated with Listeria monocytogenes.
- Class I
Medical Device Recall · February 18, 2026
Purge Cassette, sold within Impella Pump Sets and Individually Packaged. Labeled and distributed in the below configurations and corresponding product codes. 1. Purge Cassette, 5 Pack; Product CodeIncreased risk of purge leaks with Generation 1 purge cassettes.
- Class I
Medical Device Recall · February 18, 2026
Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., LtdIf heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by placing pad under the body, then the high limit device is unable to sense the higher temperature so power is not terminated. May cause a burning smell prior to melting/burning potentially causing burns to persons and property.
- Class II
Medical Device Recall · February 18, 2026
CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113, 3549313, 354-9314 SILTEX Low Height Tissue Expander Style (9100, 450cc), (9300, 450cc), (9300, 550cc)Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
- Class II
Medical Device Recall · February 18, 2026
Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585 Product Description: Aptima HPV assay Component: NoDue to product exhibiting potential to generate either invalid or false negative results.
- Class II
Drug Recall · February 18, 2026
MAXIMUM, ZONE 1, 4% Lidocaine Cream, 1/2 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-014.Stability Data Does Not Support Expiry Date.
- Class II
Medical Device Recall · February 18, 2026
Artoura Breast Tissue Expanders Reference Numbers: SDC-100UH SDC-110UH SDC-120UH SDC-130UH SDC-135UH SDC-140UH Smooth Ultra High Profile Tissue Expander, 350cc, 455cc, 535cc, 650cc, 700cc, 850ccInfusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
- Class II
Medical Device Recall · February 18, 2026
Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC-155H Smooth High Profile Tissue Expander, 225cc, 300cc, 375cc, 475cc, 500cc, 600Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
- Class III
Drug Recall · February 18, 2026
Nilotinib Capsules, 200 mg per capsule, packaged in cartons, Rx only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, Outer carton: 112 capsules (4 individuaFailed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.
- Class I
Medical Device Recall · February 18, 2026
Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory Therapy system.Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of a possible decrease in oxygen levels (oxygen desaturation), or potential lung tissue injury from overexpansion (barotrauma) when the Volara device is used in the home care environment. This correction is providing the home caregiver specific instructions for use.
- Class III
Drug Recall · February 18, 2026
Nilotinib Capsules, 150 mg per capsule, packaged in cartons, Rx only, Manufactured by: Cipla Ltd., Verna, Goa, India, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NFailed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.
- Class II
Medical Device Recall · February 18, 2026
Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software version 3.2.0.1 Product Description: Welch Allyn Spot VisiDisplay screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals.