Safety Recalls

15,186 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 2,101–2,150 of 15,186

• Vehicle Recall · February 6, 2026

  Kia America, Inc.

  2027 KIA TELLURIDE, 2027 KIA TELLURIDE HYBRID

  A seat belt strap that does not extend can fail to restrain an occupant in a crash, increasing the risk of injury.

  Unclassified

• Food Recall · February 6, 2026

  Valley Springs Artesian Gold, LLC

  Valley Springs Steamed Distilled Water. 1 Gal Net, 128 Fl. Oz. UPC 0 31193-00601 2. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901.

  Water was bottled under insanitary conditions.

  Class II

• Medical Device Recall · February 6, 2026

  Trividia Health, Inc.

  Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX AIR Kit/REA4001-01, Leader TRUE METRIX AIR Kit/RE

  The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose.

  Class I

• Medical Device Recall · February 6, 2026

  Trividia Health, Inc.

  Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX GO Kit/RF4001-01BK, CVS TRUE METRIX GO Kit/RF4007

  The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose.

  Class I

• Medical Device Recall · February 6, 2026

  Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha

  Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CR

  Software anomaly in the patient positioning system may result in positional discrepancy.

  Class II

• Vehicle Recall · February 6, 2026

  Nova Bus (US) Inc.

  2023 NOVA BUS LFS

  A low brake air pressure warning light that fails to illuminate when the engine is off will not alert the driver to a low brake pressure condition, increasing the risk of a crash if the parking brake is disengaged before starting the engine.

  Unclassified

• Vehicle Recall · February 6, 2026

  Braun Corporation

  2023 CHRYSLER VOYAGER, 2023 CHRYSLER PACIFICA, 2024 CHRYSLER PACIFICA, 2025 CHRYSLER PACIFICA, 2026 CHRYSLER PACIFICA

  The unintended connection may prevent the air bags from deploying, increasing the risk of injury during a crash.

  Unclassified

• Food Recall · February 6, 2026

  Valley Springs Artesian Gold, LLC

  Valley Springs 100% Natural Bottled Water. Fluoride Added. 1 Gal Net, 128 Fl. Oz. UPC 0 31193-01301 0. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901.

  Water was bottled under insanitary conditions.

  Class II

• Medical Device Recall · February 6, 2026

  BD KIESTRA LAB AUTOMATION

  BD Kiestra" ReadA; Catalog No.: 446948.

  In certain situations, following a system reboot, one or more modules may have become unreachable via the remote connectivity interface. When this occurred, there was potential for delays in plate retrieval from the incubator while connectivity was restored. This issue was intermittent and did not affect test results, performance of the assay, or sample integrity.

  Class II

• Medical Device Recall · February 6, 2026

  Datascope Corp.

  Battery Charging Station; Model: 0998-00-0802;

  The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to operate the IABP. Getinge has identified that a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging. The right bay of the Battery Charging Station is not affected by this issue.

  Class III

• Medical Device Recall · February 6, 2026

  Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha

  Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR

  Software anomaly in the patient positioning system may result in positional discrepancy.

  Class II

• Medical Device Recall · February 6, 2026

  International Life Sciences

  Artelon FlexBand Plus Ref: 41054 & 41057

  Augmentation devices failed bacterial endotoxin testing.

  Class II

• Medical Device Recall · February 6, 2026

  Trividia Health, Inc.

  Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX Kit/RE4001-01, Leader TRUE METRIX Kit/RE4002-01,

  The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose.

  Class I

• Consumer Product Recall · February 5, 2026

  Guangzhou Tenghui Fragrance & Flavor Co., Ltd., of China

  Lotus Joy Organic Sweet Birch Essential Oil Bottles

  The essential oil bottles contain methyl salicylate, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The bottles are not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.

  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 Barstools

  The 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

  Aterian, Inc., of Summit, New Jersey

  PurSteam Mighty Lil Steamers and PurSteam Elite Travel Steamers

  The steamers can expel hot water from the steam nozzle during use, posing a serious burn hazard to consumers.

  Unclassified

• Consumer Product Recall · February 5, 2026

  Guangzhou Feifan Kuajing Supply Chain Co., Ltd. dba Gumili Beauty, of China

  GM Gumili Wintergreen Essential Oil Bottles

  The essential oil contains methyl salicylate, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging for the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.

  Unclassified

• Consumer Product Recall · February 5, 2026

  Kitosun Original Company Limited, dba Kitosun, of China

  Kitosun Submersible LED Lights

  The 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

• Drug Recall · February 5, 2026

  Fresenius Kabi Compounding, LLC

  vancomycin HCl, 1.5 grams, 1.5 grams added to 500 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-016-59

  Lack of Assurance of Sterility

  Class II

• Drug Recall · February 5, 2026

  Fresenius Kabi Compounding, LLC

  vancomycin HCl, 2 grams, 2 grams added to 500 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-019-59.

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · February 5, 2026

  Remel, Inc

  Campy CVA Medium 100/PK, R01272

  Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.

  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 71506-035-56

  Lack of Assurance of Sterility

  Class II

• Consumer Product Recall · February 5, 2026

  Shanghai Taiye Furniture Co., Ltd., dba Furnulem, of China

  Furnulem 5-Drawer Dressers

  The 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

• Food Recall · February 5, 2026

  IF Holding II, LLC

  tippy toes apple pear banana 6 months & up baby food 2-4OZ (113g) PACKS NET WT 8 OZ (226g) DISTRIBUTED BY TOPCO ASSOCIATES LLC ELK GROVE VILLAGE, IL 60007 1-888-423-0139 PRODUCT OF USA UPC: 03680026

  Potential contamination with patulin.

  Class II

• Consumer Product Recall · February 5, 2026

  Salvia Cosmeceuticals, of India

  Organic Zing Birch Oil Bottles

  The essential oil bottles contain methyl salicylate, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The bottles for the products are not child resistant, posing a risk of poisoning if the contents are swallowed by young children.

  Unclassified

• Drug Recall · February 5, 2026

  Fresenius Kabi Compounding, LLC

  thiamine HCl, 500 mg, 500 mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-079-56.

  Lack of Assurance of Sterility

  Class II

• Drug Recall · February 5, 2026

  Fresenius Kabi Compounding, LLC

  ketamine HCl, 1,000 mg, 1,000 mg per 100 mL (10 mg per mL) in Sodium Chloride Injection, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-050-56

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · February 5, 2026

  Diagnostica Stago, Inc.

  Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF 00515 Product Description: in vitro diagnostic. The STA - Liatest D-Di kit is an assay for the quantitative det

  After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range.

  Class II

• Consumer Product Recall · February 5, 2026

  Andy & Evan Industries, Inc., of New York City, New York

  Andy & Evan Children's Pajama Sets

  The 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 Ammunition

  The 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

  Shenzhenmengzhongfeikejiyouxiangongsi doing business as Flyindream, of China

  Cobelae Busy Book for Toddlers

  The toy books violate the small parts ban because the beads can loosen and detach from the product, posing a deadly choking hazard.

  Unclassified

• Consumer Product Recall · February 5, 2026

  Wenxi Xuefeng Technology Co., Ltd, dba Dresbe, of China

  Dresbe LED Christmas Headbands

  The 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

  Changzhou Xunchuang Home Furnishing Co., Ltd., dba Momok of China

  Fixwal 7-Drawer Dressers

  The 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

  Xuzhou Mingquanhe Home Furnishing Co., Ltd., of China

  EnHomee 10-Drawer Dressers

  The 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 required by the STURDY Act.

  Unclassified

• Consumer Product Recall · February 5, 2026

  Little Cow Company LLC, of Portland, Oregon

  Little Cow Co. 9 oz candles in glass jars

  The glass jar holding the candle can crack or break during use, posing fire, burn and laceration hazards.

  Unclassified

• Consumer Product Recall · February 5, 2026

  Lola Plus The Boys Inc., of Chicago, Illinois

  Lola + The Boys Youth Clothing with Drawstrings

  The drawstrings in the recalled clothing can get caught on objects and cause death or serious injury to children due to the strangulation hazard. The clothes are in violation of the federal rule for children's upper outerwear and present a substantial product hazard.

  Unclassified

• Consumer Product Recall · February 5, 2026

  Jinjiangshi XunMai Network Technology Co., Ltd., dba Semfri, of China

  Semfri Children's Helmets

  The 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.

  Unclassified

• Consumer Product Recall · February 5, 2026

  Huizhou Sunhouse Home Furnishings Co., Ltd., of China

  Shintenchi 6-Drawer Dressers

  The 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 Dressers

  The 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

• Medical Device Recall · February 4, 2026

  Fresenius Kabi USA, LLC

  The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.

  Potential for the Cassette Loading Lever to break.

  Class II

• Vehicle Recall · February 4, 2026

  Keystone RV Company

  2026 KEYSTONE MONTANA

  A detached underbelly can become a road hazard for other vehicles, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · February 4, 2026

  Diagnostica Stago, Inc.

  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 o

  The 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.

  Class II

• Vehicle Recall · February 4, 2026

  BMW of North America, LLC

  2023 BMW K 1600 B, 2024 BMW K 1600 B

  An overheated reverse gear control unit increases the risk of a fire.

  Unclassified

• Vehicle Recall · February 4, 2026

  General Motors, LLC

  2023 CHEVROLET MALIBU, 2024 CHEVROLET MALIBU, 2025 CHEVROLET MALIBU

  A rearview image that does not display correctly reduces the driver's view behind the vehicle, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · February 4, 2026

  3B Medical, Inc.

  React Health PHOENIX 5L Oxygen Concentrator

  Devices which did not meet internal quality specifications were inadvertently distributed.

  Class II

• Vehicle Recall · February 4, 2026

  General Motors, LLC

  2025 CHEVROLET CORVETTE, 2026 CHEVROLET CORVETTE COUPE

  The driver may be unaware that the turn signal is not working, increasing the risk of a crash.

  Unclassified

• Drug Recall · February 4, 2026

  SOMERSET THERAPEUTICS LLC

  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: 70069-02

  Failed 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

• Consumer Product Recall · February 4, 2026

  Mameix Retail, Inc. of Canada

  Scepter Gas and Oil Combination Fuel Containers

  The 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.

  Unclassified

• 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 0680334993607

  Label lists semolina and durum flour as sub-ingredients of the pasta, but does not declare wheat

  Class II

• Medical Device Recall · February 3, 2026

  Exactech, Inc.

  Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/Catalog Number: KIT-311X

  Impactor handle may be missing cross-pin

  Class II