Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 6,001–6,050 of 15,271
- Unclassified
Consumer Product Recall · June 18, 2025
Shenzhen Yumo Commerce and Trade Corporation, of China
MaxKare Electric BlanketsThe recalled blankets can overheat and ignite, posing burn and fire hazards.
- Unclassified
Consumer Product Recall · June 18, 2025
Shenzhen Leader-Union Technology Co. Ltd., of China
YaFiti 12-Drawer White DressersThe recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers violate the federal standard as required by the STURDY Act.
- Unclassified
Consumer Product Recall · June 18, 2025
Sichuanyongzhichengguojimaoyiyouxiangongsi, d/b/a TADAKAZU, of China
TADAKAZU Baby LoungersThe recalled portable baby loungers violate the federal safety standards for Infant Sleep Products because the sides are shorter than the minimum side height limit to secure the infant; the sleeping pad's thickness exceeds the maximum limit, posing a suffocation hazard; and an infant could fall out of an enclosed opening at the foot of the lounger or become entrapped. The portable loungers do not have a stand, posing a fall hazard. These violations create an unsafe sleeping environment for infants, posing a risk of serious injury or death.
- Class II
Medical Device Recall · June 17, 2025
KWIK-STIK and LYFO DISK, quality control kit for culture media Catalog # 0805K and 0805LAffected products contain Staphylococcus epidermidis instead of the expected Brevundimonas diminuta. This may cause the user's quality control to fail and delayed diagnosis for the patient.
- Class II
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- Class II
Medical Device Recall · June 17, 2025
Medtronic SmartLink Software loaded on SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Azure Astra application, Software Model Number D00U003; 2. PerceA software update for Medtronic CareLink SmartSync Device Manager (SmartSync) is now available. The update eliminates the potential display of an erroneous electrical reset (pop-up) message upon interrogation with a SmartSync Device Manager. The erroneous message indicates an electrical reset has occurred. However, no reset has actually occurred and there are no parameter changes or loss of diagnostics. Prior to this software update, if an erroneous SmartSync message was displayed, confusion regarding the message could have caused a clinician to consider an unnecessary system revision. Medtronic has received 39 reports of this display error with two instances of unnecessary device explant through 30 April 2025.
- Class II
- Class II
- Class II
Food Recall · June 17, 2025
Reisman's 2/pk Soft Chip Cookie (with fudge filling) 3 oz.Undeclared wheat
- Class II
- Class I
Food Recall · June 17, 2025
Passion Fruit Mousse, NET WT 8 OZ (230g), Sabores Bakery, Plastic Cups, 3.5-inch-wide x 3.75 in high, Keep refrigerated, PRODUCED EXCLUSIVELY BY: SABORES FIT BAKERY LLC. ORLANDO, FL 32836, UPC 7 35816Undeclared allergens: Milk, Eggs, Soy Ingredients (Soybean oil, Soy Lecithin), Wheat, Tree Nuts (Almonds, Hazelnuts) on label and incomplete Contains statement
- Class I
Food Recall · June 17, 2025
Four Milk Mousse, NET WT 8 OZ (230g), Sabores Bakery, Plastic Cups, 3.5-inch-wide x 3.75 in high, Keep refrigerated, PRODUCED EXCLUSIVELY BY: SABORES FIT BAKERY LLC. ORLANDO, FL 32836, UPC 7 35816 971Undeclared allergens: Milk, Eggs, Soy Ingredients (Soybean oil, Soy Lecithin), Wheat, Tree Nuts (Almonds, Hazelnuts) on label and incomplete Contains statement
- Class II
- Class II
- Class II
- Class I
Food Recall · June 17, 2025
Choco Mousse, NET WT 8 OZ (230g), Sabores Bakery, Plastic Cups, 3.5-inch-wide x 3.75 in high, Keep refrigerated, PRODUCED EXCLUSIVELY BY: SABORES FIT BAKERY LLC. ORLANDO, FL 32836, UPC 7 35816 97176 2Undeclared allergens: Milk, Eggs, Soy Ingredients (Soybean oil, Soy Lecithin), Wheat, Tree Nuts (Almonds, Hazelnuts) on label and incomplete Contains statement
- Class II
Food Recall · June 17, 2025
Bake-a-holic Pecan Bars Cheesecake Royale Pecan BarsReview of Label determined allergen was listed as unsalted butter/ heavy cream. In one instance of identified label, there was no milk or dairy listed listed in Contains statement. Further review of label revealed "soy" had been removed.
- Class II
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- Class I
Food Recall · June 17, 2025
Three Milk Mousse, NET WT 8 OZ (230g), Sabores Bakery, Plastic Cups, 3.5-inch-wide x 3.75 in high, Keep refrigerated, PRODUCED EXCLUSIVELY BY: SABORES FIT BAKERY LLC. ORLANDO, FL 32836, UPC 7 35816 97Undeclared allergens: Milk, Eggs, Soy Ingredients (Soybean oil, Soy Lecithin), Wheat, Tree Nuts (Almonds, Hazelnuts) on label and incomplete Contains statement
- Class II
- Class I
Food Recall · June 17, 2025
Strawberry Mousse, NET WT 8 OZ (230g), Sabores Bakery, Plastic Cups, 3.5-inch-wide x 3.75 in high, Keep refrigerated, PRODUCED EXCLUSIVELY BY: SABORES FIT BAKERY LLC. ORLANDO, FL 32836, UPC 7 35816 97Undeclared allergens: Milk, Eggs, Soy Ingredients (Soybean oil, Soy Lecithin), Wheat, Tree Nuts (Almonds, Hazelnuts) on label and incomplete Contains statement
- Class II
- Class II
- Class II
- Class I
Medical Device Recall · June 17, 2025
i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.Potential for faulty devices as a result of depleted batteries.
- Class II
Medical Device Recall · June 17, 2025
QuickVue: Dipstick Strep A Test: 50T, REF: 20108; 25T, REF: 20125; 50T, SCN, REF: 20108SCDipstick strep A test has potential for false positive results.
- Class II
Medical Device Recall · June 17, 2025
MI Cancer Seek REF MSC000 UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Seek is a single-site assay intended to provide tumor mutational profiling to be used by qualified healthcare professiDue to an incorrect test results provided that indicated the incorrect drug therapy recommendation
- Class II
Medical Device Recall · June 17, 2025
Medtronic SmartLink software loaded on CareLink SmartSync Device Manager, Model Number 24967A with the following software components: 1. Azure Astra application, Software Model Number D00U003; 2A software update for Medtronic CareLink SmartSync Device Manager (SmartSync) is now available. The update eliminates the potential display of an erroneous electrical reset (pop-up) message upon interrogation with a SmartSync Device Manager. The erroneous message indicates an electrical reset has occurred. However, no reset has actually occurred and there are no parameter changes or loss of diagnostics. Prior to this software update, if an erroneous SmartSync message was displayed, confusion regarding the message could have caused a clinician to consider an unnecessary system revision. Medtronic has received 39 reports of this display error with two instances of unnecessary device explant through 30 April 2025.
- Class II
Medical Device Recall · June 16, 2025
InPen App, CFN: MMT-8060 (iOS Users) and MMT-8061 (Android Users)Medtronic MiniMed, Inc. is recalling InPen App for iOS and Android users due to software design errors that could lead to a missed short-acting insulin dose reminder and a recommendation to correct a high glucose value. It does not impact insulin delivery, long-acting insulin dose reminders, or CGM alerts, and users can still use the pen itself to calculate a dose, deliver insulin, record the dose date/time, and view CGM data. This issue was identified during internal testing before release in the US but after release to OUS customers, no complaints or MDRs related to this recall have been reported. Use of the affected device may result hyperglycemia by failing to alert the user and delay treatment of diabetes.
- Class I
Medical Device Recall · June 16, 2025
SafeStar 55 Plus Filter. Bidirectionally breathing system filter.Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
- Class II
Medical Device Recall · June 16, 2025
Biofinity XR Toric Contact LensLens blisters may have an incomplete or leaking seal which may render them unsterile.
- Class II
Drug Recall · June 16, 2025
SUN PHARMACEUTICAL INDUSTRIES INC
Lisdexamfetamine Dimesylate Capsules, 60 mg, CII, 100-count bottles, Rx only, Manufactured by: OHM Laboratories, New Brunswick, NJ 08901, Distributed by: Sun Pharmaceuticals, Inc., Cranbury, NJ 08512,Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 9 month long term stability station (25¿C, 60%RH).
- Class II
Medical Device Recall · June 16, 2025
Biofinity Toric Multifocal Contact LensLens blisters may have an incomplete or leaking seal which may render them unsterile.
- Class I
Food Recall · June 16, 2025
D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds), 25lb Bulk Cases Packaged into Various Size Units After distribution.undeclared milk allergen
- Class I
Medical Device Recall · June 16, 2025
SafeStar 60A Plus Filter. Bidirectionally breathing system filter.Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
- Class II
Drug Recall · June 16, 2025
0.9% Sodium Chloride Injection USP, 500 mL, packaged in 500 mL excel containers and further packaged 24 per case, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC 0264-7800-10.Lack of assurance of sterility: pinholes, within the finger boxes used during Form Fill Seal process resulting in leaks.
- Class III
Drug Recall · June 16, 2025
Testosterone 200 mg Pellet packaged in 1mL amber vials, Rx only, Compounded product. Qualgen 14844 Bristol Park Blvd Edmond OK 73013, NDC 69761-202-01Labeling: Incorrect or Missing Lot and/or Exp. Date: A printing issue resulted in incorrect lot numbers on the label.
- Class I
Medical Device Recall · June 16, 2025
SafeStar 90 Plus Filter. Bidirectionally breathing system filter.Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.