Safety Recalls
RSS ↗17,559 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 3,601–3,650 of 17,559
- Class I
Food Recall · February 11, 2026
Junebar Peanut Chocolate Chip All Natural Snack Bar; INGREDIENTS: ORGANIC PEANUT BUTTER, DATE PASTE, ORGANIC BLACK BEANS, ORGANIC SWEET POTATOES, GLUTEN FREE ROLLED OATS, SEMI-SWEET SOY FREE VEGAN SHOProducts contain undeclared milk and soy.
- Class II
Medical Device Recall · February 11, 2026
Burlington Medical, Half Aprons.Potential for attenuation degradation over time, decreasing the lifespan.
- Class II
Medical Device Recall · February 10, 2026
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee SystemDrill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
- Class II
Medical Device Recall · February 10, 2026
Artegraft Vascular Graft; REF#: AG740;Labeling mix-up resulting in the incorrect lot outer packaging of product.
- Unclassified
Vehicle Recall · February 10, 2026
2025 VOLVO VNL (4), 2026 VOLVO VNL (4)Inadequate parking brake force can result in a rollaway, increasing the risk of a crash.
- Class II
Medical Device Recall · February 10, 2026
Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2" MSC8622EP DRESSING,COLLAGEN,PURACOL PLUS, 2X2.2"Elevated endotoxin levels identified in affected lots. Issue may elicit strong inflammatory response if used, including local tissue irritation, delayed wound healing, or systemic effects such as fever and hypotension. In severe cases, septic shock may result.
- Class II
Food Recall · February 10, 2026
VERGANI 1944 MILANO 'PANDORO CLASSICO' Gluten Free, 600g NET WT. 1 LBS. 5.2 OZ., packaged in paper cartons, 6 units per case. Lot 217666, UPC 8002114019833Potential contamination with foreign material (Teflon fragments) from flaking cooking molds.
- Class II
Drug Recall · February 10, 2026
Adbry, (tralokinumab-ldrm) injection, 300 mg/2mL, Packaged as a) 1 x Single dose Autoinjector, SAMPLE NOT FOR SALE, NDC 50222-350-91; b) 2 x Single dose Autoinjectors, NDC 50222-350-02; Rx only, ManuLack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.
- Class II
Medical Device Recall · February 10, 2026
EndoVive Safety PEG Kit; Outer Box Material Number (UPN): M00509001; Inner Box Material Number (UPN): M00509000;Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open or compromised seals on the sterile swabstick packaging, which could result in loss of sterility or drying of the antiseptic solution. This component is placed outside of the sterile barrier of the tray manufactured by Boston Scientific, which contains the majority of the kit components. As such, inclusion of the affected ChloraPrep Triple Swabsticks does not degrade the integrity of the other components within the PEG kit.
- Class II
Food Recall · February 10, 2026
Wellsley Farms Farm- Raised Atlantic Salmon Net WT. 32 oz. (2 lbs.) 907 gContaminated with Listeria monocytogenes
- Class II
Medical Device Recall · February 10, 2026
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee SystemDrill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
- Unclassified
Vehicle Recall · February 9, 2026
2023 HARLEY-DAVIDSON RH1250S, 2024 HARLEY-DAVIDSON RH1250S, 2026 HARLEY-DAVIDSON RH1250SAn upper triple clamp that fractures can lead to a loss of control, increasing the risk of a crash.
- Class II
Medical Device Recall · February 9, 2026
Abbott Diagnostics Scarborough, Inc.
Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applicable Product Description: Influenza A/B virus nucleic acid IVD, kit, nucleic acid technique ComponIt was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.
- Class II
Drug Recall · February 9, 2026
Cetrorelix Acetate for Injection (Kit), 0.25 mg per vial, Single-Dose Kit, Rx Only, Mfd. for: Meitheal Pharmaceuticals, Chicago, IL NDC 71288-558-90.Defective Delivery System: Missing or duplicated needles within the injection kit
- Class II
Medical Device Recall · February 9, 2026
RefleXion X1 Radiotherapy System Model RXM1000, Part #800-00006-00Due to a radiotherapy medical system software defect, when performing angular roll corrections followed by a repeat localization, the roll corrections applied in the initial localization scan are not carried through to treatment delivery leading to the treatment plan dose being delivered to the incorrect location, potentially a displacement of 5mm or higher, with a 10% to 20% underdose.
- Unclassified
Consumer Product Recall · February 9, 2026
Airova, Inc. of Newark, California
Aroeve brand air purifiersThe air purifiers can overheat and ignite, posing fire and burn hazards to consumers.
- Class II
Food Recall · February 9, 2026
Hortex Mieszanka 9 - skBadnikowa Spring vegetable mix with 9 ingredients, net wt 15.87oz., UPC 5 900477 018735 >, 14 units per casepotential contamination with glass
- Class II
Food Recall · February 9, 2026
Frozen Cooked Medium Shrimp Peeled & Deveined, Tail Off-White Shrimp; 1 lbs retail plastic bag. UPC: 041220333035Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
- Class I
Food Recall · February 8, 2026
Lobster & Crab Ravioli. Keep Frozen. Contains: Wheat, Eggs, Milk, Crustaceans-Shellfish. Product is intended to be further cooked. Weight: 1-10 pound (4.5g). Use within 6 months. 801-541-9292-www.FuUndeclared shrimp, crab, lobster, pollock (fish), whiting (fish), and soy.
- Class I
Medical Device Recall · February 6, 2026
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/RF4007The 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 II
Medical Device Recall · February 6, 2026
Artelon FLEXBAND TWIST .12 Ref: TW012 3.85x17mm HEX Anchor (Qty 2) 5.0x17mm HEX Anchor (Qty 1) 0.5x12cm FLEXBAND (Qty 1)Augmentation devices failed bacterial endotoxin testing.
- Class III
Medical Device Recall · February 6, 2026
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.
- Unclassified
Vehicle Recall · February 6, 2026
2025 HYUNDAI IONIQ 5An electrical short in the high voltage battery system increases the risk of a fire.
- Class II
Medical Device Recall · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057Augmentation devices failed bacterial endotoxin testing.
- Class I
Medical Device Recall · February 6, 2026
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
Medical Device Recall · February 6, 2026
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/REThe 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 II
Medical Device Recall · February 6, 2026
Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FRSoftware anomaly in the patient positioning system may result in positional discrepancy.
- Class II
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" 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
Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CRSoftware anomaly in the patient positioning system may result in positional discrepancy.
- Class I
Medical Device Recall · February 6, 2026
Owner's Booklets and Instructions for Use that are used with the following blood glucose measurement devices. Description/Item: TRUE METRIX PRO Meter Only/RE4H01P-40, TRUE METRIX PRO Starter Kit/REThe 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 II
Medical Device Recall · February 6, 2026
Artelon FlexBand Plus Ref: 41054 & 41057Augmentation devices failed bacterial endotoxin testing.
- Class II
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
Food Recall · February 6, 2026
Valley Springs Artesian Gold, LLC
Valley Springs 100% Natural Bottled Water packaged in the following size plastic jug with plastic caps: 1. 1 Gal Net 128 Fl oz. UPC 0 31193-00701 9. Bottled by Valley Springs/Artesian Gold, LLCWater was bottled under insanitary conditions.
- Unclassified
Consumer Product Recall · February 5, 2026
Xuzhou Mingquanhe Home Furnishing Co., Ltd., of China
EnHomee 10-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 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 jarsThe 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 DrawstringsThe 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
Huizhou Sunhouse Home Furnishings Co., Ltd., of China
Shintenchi 6-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
Guangzhou Tenghui Fragrance & Flavor Co., Ltd., of China
Lotus Joy Organic Sweet Birch Essential Oil BottlesThe 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.
- Class II
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
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 71506-016-59Lack 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
- Unclassified
Consumer Product Recall · February 5, 2026
Guangzhou Feifan Kuajing Supply Chain Co., Ltd. dba Gumili Beauty, of China
GM Gumili Wintergreen Essential Oil BottlesThe 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.
- 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 71506-050-56Lack of Assurance of Sterility
- Unclassified
Consumer Product Recall · February 5, 2026
Shenzhenmengzhongfeikejiyouxiangongsi doing business as Flyindream, of China
Cobelae Busy Book for ToddlersThe 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
Salvia Cosmeceuticals, of India
Organic Zing Birch Oil BottlesThe 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.
- Class II
Medical Device Recall · February 5, 2026
Campy CVA Medium 100/PK, R01272Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
- Class II
Medical Device Recall · February 5, 2026
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 detAfter receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range.
- Class II
Food Recall · February 5, 2026
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: 03680026Potential contamination with patulin.
- Unclassified
Consumer Product Recall · February 5, 2026
Aterian, Inc., of Summit, New Jersey
PurSteam Mighty Lil Steamers and PurSteam Elite Travel SteamersThe steamers can expel hot water from the steam nozzle during use, posing a serious burn hazard to consumers.