Safety Recalls
RSS ↗17,559 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 3,651–3,700 of 17,559
- Unclassified
Consumer Product Recall · February 5, 2026
Clark Core Services LLC, dba Clark Associates, of Lancaster, Pennsylvania
Lancaster Table & Seating Powder-Coated Aluminum Outdoor Chairs and BarstoolsThe legs of the chairs and barstools can bend or break while the chair is in use, posing a fall hazard.
- Unclassified
Consumer Product Recall · February 5, 2026
Wenxi Xuefeng Technology Co., Ltd, dba Dresbe, of China
Dresbe LED Christmas HeadbandsThe recalled headbands violate the mandatory standard for consumer products with button cell and coin batteries because the button cell batteries in the headbands can be accessed easily by children, posing an ingestion hazard. Additionally, the packaging and product do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.
- Unclassified
Consumer Product Recall · February 5, 2026
Shanghai Taiye Furniture Co., Ltd., dba Furnulem, of China
Furnulem 5-Drawer DressersThe recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory standard as required by the STURDY Act.
- Unclassified
Consumer Product Recall · February 5, 2026
Kitosun Original Company Limited, dba Kitosun, of China
Kitosun Submersible LED LightsThe recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain lithium coin batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings as required by Reese's Law. When children swallow button cell or coin batteries, the ingested batteries can cause serious injuries, internal chemical burns, and death, posing an ingestion hazard to children.
- Unclassified
Consumer Product Recall · February 5, 2026
Jinjiangshi XunMai Network Technology Co., Ltd., dba Semfri, of China
Semfri Children's HelmetsThe recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional stability, labeling 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
Drug Recall · February 5, 2026
Fresenius Kabi Compounding, LLC
acyclovir sodium, 200 mg, 200mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, For Intravenous Use, Single-Use Bag, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-035-56Lack of Assurance of Sterility
- Unclassified
Consumer Product Recall · February 5, 2026
Andy & Evan Industries, Inc., of New York City, New York
Andy & Evan Children's Pajama SetsThe recalled children's pajamas violate the mandatory flammability standard for children's sleepwear, posing a risk of serious burn injuries or death.
- Unclassified
Consumer Product Recall · February 5, 2026
DriBiz LLC, Fairview Heights, Illinois
Ammo Tabs Fiber Desiccant Tiles used for Firearms and AmmunitionThe Ammo Tab can fail to protect the firearms and ammunition from humidity, allowing excess moisture to cause corrosion or rust that can increase the risk of malfunction and pose an injury hazard.
- Unclassified
Consumer Product Recall · February 5, 2026
Changzhou Xunchuang Home Furnishing Co., Ltd., dba Momok of China
Fixwal 7-Drawer DressersThe recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory standard as required by the STURDY Act.
- Unclassified
Consumer Product Recall · February 5, 2026
Yita LLC, dba Yitahome, Uforic, Dextrus, Yintatech and ModFusion, of Kent, Washington
Yitahome, Uforic, Dextrus, Yintatech and ModFusion-branded DressersThe recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory standard as required by the STURDY Act.
- Unclassified
Consumer Product Recall · February 4, 2026
Scepter Gas and Oil Combination Fuel ContainersThe recalled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under the Portable Fuel Container Safety Act, posing a deadly risk of flash fire. In addition, the Children's Gasoline Burn Prevention Act requires all closures on portable gasoline fuel containers to be child resistant. The spout on the product is not child-resistant, posing a risk of burn and poisoning to children.
- Class II
Drug Recall · February 4, 2026
Dexamethasone Sodium Phosphate Injection, USP, 100 mg/ 10 mL, (10 mg/mL), 10x10 mL Multiple Dose Vials, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873, NDC carton: 70069-02Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were above specs for these impurities: Dexamethasone Sodium Phosphate EP impurity G (Impurity RU 49336) and dexamethasone formate.
- Class II
Medical Device Recall · February 4, 2026
Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Number (REF): 00516 Product Description: The STA¿ - Liatest¿ Free Protein S kits are intended for use oThe potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects normal-range values.
- Unclassified
Vehicle Recall · February 4, 2026
2025 CHEVROLET CORVETTE, 2026 CHEVROLET CORVETTE COUPEThe driver may be unaware that the turn signal is not working, increasing the risk of a crash.
- Unclassified
Vehicle Recall · February 4, 2026
2025 FREIGHTLINER BUSINESS CLASS M2A lack of lubrication may cause binding gears and difficulty steering, increasing the risk of a crash.
- Class II
Medical Device Recall · February 4, 2026
React Health PHOENIX 5L Oxygen ConcentratorDevices which did not meet internal quality specifications were inadvertently distributed.
- Class II
Medical Device Recall · February 4, 2026
The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.Potential for the Cassette Loading Lever to break.
- Unclassified
Vehicle Recall · February 4, 2026
Ember Recreational Vehicles, INC
2026 EMBER E-SERIESIncorrect weight information may lead to unintentionally overloading the vehicle, increasing the risk of a crash.
- Class III
Drug Recall · February 3, 2026
Pitavastatin Tablets, 2 mg, packaged in 90-count bottles, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Annora Pharma Pvt. LTd., Sengareddy - 502313, Telengana, IndiPresence of foreign tablets/capsules: one Pitavastatin tablet 1mg found in bottle of Pitavastatin tablets 2mg
- Class II
Medical Device Recall · February 3, 2026
Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/Catalog Number: KIT-311XImpactor handle may be missing cross-pin
- Class II
Food Recall · February 3, 2026
Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid dietary supplement, Glass bottle with dropper cap. (Individual 1 fl oz bottles (not solLabel declares bovine colostrum but does not declare milk allergen.
- Class II
Food Recall · February 3, 2026
Cocos Wholesale and Imports, LLC
Coco's Italian Market Cannoli Making Kit with 6 Cannoli Shells & Cream, Net Wt. 8 oz. (227g), Keep Frozen, packaged in a plastic container, UPC 0680334992716Label lists flour as a sub-ingredient of the shells, and ricotta cheese as a sub-ingredient of the cream but does not declare wheat or milk.
- Class II
Medical Device Recall · February 3, 2026
Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Numbers E85101LA and E85101LPThere is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position.
- Class II
Medical Device Recall · February 3, 2026
IBA Proton Therapy System - PROTEUS 235It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration. In this condition, the TSS does not interrupt the beam delivery if the Healthy Signal from an external gating device is lost. This may lead to a risk of mistreatment when external gating devices are used.
- Class II
Food Recall · February 3, 2026
Cocos Wholesale and Imports, LLC
Coco's Italian Market Heat-n-Eat Fettuccini Alfredo in homemade Alfredo Sauce, Net Wt. 19 oz. (510g), Keep Frozen, packaged in a microwaveable plastic container, UPC 0680334993607Label lists semolina and durum flour as sub-ingredients of the pasta, but does not declare wheat
- Class II
Medical Device Recall · February 3, 2026
Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05Impactor handle may be missing cross-pin
- Unclassified
Vehicle Recall · February 2, 2026
2024 JEEP WAGONEER S, 2025 JEEP WAGONEER S, 2025 RAM 5500, 2025 RAM 3500, 2026 RAM 3500Trailer brake lights and turn signals that do not illuminate reduce visibility to other drivers, increasing the risk of a crash. Additionally, trailer brakes that fail increase the risk of a crash.
- Class II
Medical Device Recall · February 2, 2026
Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intenThe potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
- Class II
Drug Recall · February 2, 2026
Pro Numb Tattoo Numbing Spray LLC
Pro Numb Tattoo Numbing Spray, 5% Lidocaine, [1 FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-111-11cGMP deviations
- Class II
Medical Device Recall · February 2, 2026
Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF Model/Catalog Number: 7B3050 Software Version: N/A Product Description: A device designed for subcutaneous implantation andThe potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
- Class II
Medical Device Recall · February 2, 2026
Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be usThe potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
- Class II
Medical Device Recall · February 2, 2026
MICS3 Angled Sagittal Saw Attachment; Part Number: 210490A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and detach from the attachment.
- Class II
Medical Device Recall · February 1, 2026
On-X Mitral Heart Valve with Conform-X Sewing Ring, Model: ONXMC-25/33Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.
- Class I
Food Recall · January 31, 2026
Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. UPC 000011 812722. Product is packaged in a clear clamshell container. ALLERGENS INFORMATION: CONTAINS WHEAT, EGG, MILK,Undeclared hazelnut.
- Class II
Medical Device Recall · January 30, 2026
Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-02There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
- Class II
Medical Device Recall · January 30, 2026
HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03 Model / UDI-DI codes: Vital Sync 3.3.1 / 10884521844933 Vital Sync 3.4.0 / 1Due to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on the remote patient monitoring system.
- Class II
Medical Device Recall · January 30, 2026
Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-406, 2There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
- Class II
Medical Device Recall · January 30, 2026
DxC 700 AU, REF: B86444, B86446A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open beyond15 minutes may lead to: Reagent Blank and calibration databases not opening errors: CAL History DB Open Error.., RB History DB Open Error..; system will stop analyzing, firm service must visit to apply software solution; may lead to delay in diagnosis and/or patient treatment.
- Unclassified
Vehicle Recall · January 30, 2026
2023 BMW X3, 2023 BMW X4, 2023 TOYOTA SUPRA, 2024 BMW 530IFire increases the risk of injury.
- Class II
Medical Device Recall · January 30, 2026
MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61Three software defects (Pump Error 53, BG check, and Critical Pump Error (Open Book Image)) that occurred as a result of software updates (versions 6.60, 6.61, and 6.62), which could result in a risk of hypoglycemia or hyperglycemia due to inaccuracies in insulin delivery (either under-delivery, over-delivery, or cessation of delivery).
- Class II
Medical Device Recall · January 30, 2026
Tandem pumps are battery-operated infusion pumps capable of both basal and bolus delivery of insulin. The pumps utilize a motor-driven mechanism to deliver insulin from within a disposable cartridge,The Czech language user guide contained multiple translation errors. The most significant error was that it incorrectly instructs users to verify that the infusion set is connected to the body, when it should instead direct users to confirm that the infusion set is not connected to the body. Following this instruction could result in unintended insulin delivery, potentially leading to a hypoglycemic event.
- Unclassified
Vehicle Recall · January 30, 2026
2025 GRAND DESIGN LINEAGEA loose seat base increases the risk of injury in the event of a crash.
- Class I
Food Recall · January 30, 2026
The Tuna Salad product container is mislabeled with a Chicken Salad lid, which states: Molly Kitchen's Chicken Salad, 789953, NET WT. 5 LB (2.26 kg) per plastic tub. UPC 7 5810830149 8. Distributed byUndeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad.
- Class II
Food Recall · January 30, 2026
Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel. Net wt: Approx: 2 oz (57g). UPC 8 55725 00514 0. Taste of Maui Snacks dba of J2C Hawaii, LLC PO Box 1023, Wailuku HI 96793. The product label iIngredients List declares peanut but the Contains statement does not declare peanut
- Class I
Food Recall · January 30, 2026
Karns Foods, Mini Dark Chocolate Raspberry Cups, 8 oz Clear plastic tamper evident packs, 36-42 packed per breakoutProduct may contain undeclared peanuts.
- Class II
Medical Device Recall · January 30, 2026
Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 5826659-027, 58There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
- Class II
Medical Device Recall · January 30, 2026
CHEMISTRY ANALYZER AU5800, REF: B96697, B96698, B23279, B23280, B23281A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open beyond15 minutes may lead to: Reagent Blank and calibration databases not opening errors: CAL History DB Open Error.., RB History DB Open Error..; system will stop analyzing, firm service must visit to apply software solution; may lead to delay in diagnosis and/or patient treatment
- Class II
Medical Device Recall · January 30, 2026
Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART, Model Number: DYNJ902487A; 2) CARDIAC PROCEDURE, Model Number: DYNJ908126; 3) CARDIO CONGENITO, Model NumbeThe instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target patient population as adults, 18 years and older.