Safety Recalls
RSS ↗17,553 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 2,501–2,550 of 17,553
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Banana Ice Cream - 32 oz; 56 ozUndeclared Milk, Yellow #5.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Mango Ice Cream - 32 oz; 56 ozUndeclared Milk, Yellow #5.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Lime Sherbert - 32 ozUndeclared Milk, Wheat, Soy, Yellow #5, Green #3.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Almond Joy Ice Cream - 32 ozUndeclared Milk, Almonds, Soy, Sulfites.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Coconut Pineapple Ice Cream - 32 oz; 56 ozUndeclared Milk.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Black Raspberry Ice Cream - 32 ozUndeclared Milk, Red #40, Blue #1.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Champagne Sherbert - 32 ozUndeclared Milk, Red #40.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Peanut Butter Fudge Ice Cream - 32 ozUndeclared Milk, Peanuts.
- Class III
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Burgundy Cherry Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00909Undeclared Red #40, Blue #1, Blue #2
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Lemon Chiffon Ice Cream - 32 ozUndeclared Milk, Eggs, Yellow #5.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Ube Ice Cream - 32 ozUndeclared Milk, Red #3, Red #40, Blue #1, Blue #2.
- Class III
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Peppermint Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00933Undeclared Red #40
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Pistachio Ice Cream - 32 ozUndeclared Milk, Pistachios, Yellow #5, Blue #1.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Chocolate Mint Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00917Undeclared Soy (with mitigating circumstances), Yellow #5, Blue #1
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Rocky Road Ice Cream - 56 ozUndeclared Milk, Walnuts, Eggs.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Chocolate Showers Ice Cream - 32 oz; 56 ozUndeclared Milk, Soy.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Orange Sherbert - 32 ozUndeclared Milk, Yellow #5.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Sea Salt Caramel Ice Cream - 32 ozUndeclared Milk, Soy, Sulfites.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Maple Walnut Ice Cream - 32 ozUndeclared Milk, Walnuts, Sulfites.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Pumpkin Ice Cream - 32 ozUndeclared Milk, Yellow #6.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Chocolate Ice Cream - 32 oz; 56 ozUndeclared Milk.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Butter Brickle Ice Cream - 32 ozUndeclared Milk, Almonds, Soy.
- Class II
Food Recall · April 15, 2026
Silver Moon LP dba Loard's Ice Cream
Loard's Horchata Ice Cream - 32 ozUndeclared Milk, Soy.
- Class II
Medical Device Recall · April 14, 2026
Philips Evolution Upgrade 1.5T with MR Elastography (MRE). 1. Model Number (REF): 782116 2. Model Number (REF): 782148. 3. Model Number (REF): 782166.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781270. 2. Model Number (REF): 782113.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+ iOS CGM App Model/Catalog Number: SW14244 Software Version: versions 1.5.0 and 1.6.0 Product Description: DexA software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app is running in the background, EGV notifications may queue up and then "replay" sequentially when the user brings the app to the foreground, causing the Glucose Compass to flicker through previous EGVs. In more severe instances, the app may perceive signal loss and deploy signal loss mitigations. This delay in EGV and alert processing creates a risk that users may miss detection of a hypoglycemic or hyperglycemic event, or make treatment decisions based on outdated glucose information.
- Class II
Medical Device Recall · April 14, 2026
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App Model/Catalog Number: SW13355 Software Version: Versions 2.9.0 through 2.11.2 Product DescriptionA software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app is running in the background, EGV notifications may queue up and then "replay" sequentially when the user brings the app to the foreground, causing the Glucose Compass to flicker through previous EGVs. In more severe instances, the app may perceive signal loss and deploy signal loss mitigations. This delay in EGV and alert processing creates a risk that users may miss detection of a hypoglycemic or hyperglycemic event, or make treatment decisions based on outdated glucose information.
- Class II
Medical Device Recall · April 14, 2026
Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120. 2. Model Number (REF): 782153.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782130.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Food Recall · April 14, 2026
Specially SELECTED brand Vanilla Creme Brulee; NET WT 3.6oz (103g); INGREDIENTS: CREAM (MILK, CREAM), FROZEN YOLK MIX (EGG YOLK, SUGAR) SUGAR, NATURAL VANILLA FLAVOR, TAPIOCA STARCH, CARRAGEENAN; TOPPProduct may contain foreign objects, specifically glass.
- Class II
Medical Device Recall · April 14, 2026
Philips Ingenia Elition S with MR Elastography (MRE). 1. Model Number (REF): 781357. 2. Model Number (REF): 782106. 3. Model Number (REF): 782137.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Philips Ingenia 1.5T CX with MR Elastography (MRE). 1. Model Number (REF): 781262.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Philips Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 781358. 2. Model Number (REF): 782107. 3. Model Number (REF): 782136. 510(k) Numbers: K213516, K223458,The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Unclassified
Vehicle Recall · April 14, 2026
2025 FORD F-53, 2026 FORD F-59A missing spindle nut may lead to brake system damage or wheel detachment, resulting in a loss of vehicle control and increasing the risk of a crash.
- Class II
Medical Device Recall · April 14, 2026
Philips Ingenia 3.0T CX with MR Elastography (MRE). 1. Model Number (REF): 781271. 2. Model Number (REF): 782105. 510(k) Numbers: K173079, K183063, K193215, K213583, K223458, K251397, K2The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Philips Achieva 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781196. 2. Model Number (REF): 781296.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Philips Achieva 1.5T Initial system with MR Elastography (MRE). 1. Model Number (REF): 781178.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Philips Ingenia 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781315. 2. Model Number (REF): 781341. 3. Model Number (REF): 781396. 4. Model Number (REF): 782115. 510(k)The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Philips Achieva 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781278.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781260. 2. Model Number (REF): 782112.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Unclassified
Vehicle Recall · April 14, 2026
2023 FORD BRONCO, 2024 FORD BRONCOExcessive wear of the transmission and transfer case splines may result in a loss of drive power or vehicle rollaway, increasing the risk of a crash.
- Class II
Medical Device Recall · April 14, 2026
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number: SW12300 Software Version: Versions 2.9.0 through 2.11.2 Product Description: DeA software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app is running in the background, EGV notifications may queue up and then "replay" sequentially when the user brings the app to the foreground, causing the Glucose Compass to flicker through previous EGVs. In more severe instances, the app may perceive signal loss and deploy signal loss mitigations. This delay in EGV and alert processing creates a risk that users may miss detection of a hypoglycemic or hyperglycemic event, or make treatment decisions based on outdated glucose information.
- Class II
Medical Device Recall · April 14, 2026
Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781342. 2. Model Number (REF): 781377. 3. Model Number (REF): 782103. 510(k) Numbers: K163116, K173079, K183063,The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class III
Drug Recall · April 14, 2026
Premier, Monsel's, Ferric Subsulfate Solution, 8 mL bottles, Rx only, Manufacturer: Premier Medical Products, 1710 Romano Drive, Plymouth Meeting, PA 19462, NDC 48783-112-08.Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14). It is important to note that this error is limited to the vial itself; the saleable unit of the box of 12 bottles has the correct expiration date printed.
- Class II
Medical Device Recall · April 14, 2026
Philips Ingenia Ambition X with MR Elastography (MRE). 1. Model Number (REF): 781356. 2. Model Number (REF): 782109. 3. Model Number (REF): 782138. 4. Model Number (REF): 782160.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Philips Evolution upgrade 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782143. 2. Model Number (REF): 782162.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Philips Ingenia Ambition S with MR Elastography (MRE). 1. Model Number (REF): 781359. 2. Model Number (REF): 782108. 3. Model Number (REF): 782139.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 14, 2026
Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 782118. 2. Model Number (REF): 782144. 3. Model Number (REF): 782163.The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
- Class II
Medical Device Recall · April 13, 2026
Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)Nitrile Exam Glove failed to meet specifications chemical permeation performance.