Safety Recalls
RSS ↗15,184 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 2,051–2,100 of 15,184
- Unclassified
Consumer Product Recall · February 12, 2026
Hangzhouyoupengmaoyiyouxiangongsi (Hangzhou Youpeng Trading Co., Ltd.), dba Babibaby, of China
CheerKid Baby Bath SeatsThe recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.
- Class III
Drug Recall · February 12, 2026
Eptifibatide Injection, 75 mg/100 mL vial for weight-adjusted bolus dosing, 1x100 mL Single-dose Vial, For Intravenous Use Only, Rx Only, Manufactured by: Hainan Poly Pharm. Co., Ltd., Guilinyang EconLabeling: Not Elsewhere Classified. The carton for Eptifibatide Injection 75 mg/100 mL states 75 mg/100 mL vial for weight-adjusted bolus dosing. The approved statement is 75 mg/100 mL vial for weight-adjusted infusion.
- Class I
Medical Device Recall · February 12, 2026
Flexible Cryoprobe (OD 1.1mm, L1.15mm) w/ oversheath (OD2.6mm, L817mm) REF: 20402-401 STERILE EO. For surgical useProbes may rupture/burst during activation
- Unclassified
Consumer Product Recall · February 12, 2026
Jet Importer: Watkins Manufacturing Corporation, of Vista, California
Hydromassage Rotary Jet (6 fin) in Highlife Collection spasThe hydromassage rotary jets can create a suction force that allows the user's hair to be entangled, submerging their head underwater, posing entanglement and drowning hazards to the user.
- Unclassified
Consumer Product Recall · February 12, 2026
Leioujiapin Technology Co., Ltd. dba Beloems, of China
Beloems Adult Portable Bed RailsThe recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. The bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard.
- Unclassified
Consumer Product Recall · February 12, 2026
TIANJINSHIHAOWEIXINSHENGJIDIANANZHUANGGONGCHENG, of China
3-Pack Smoke Detector Fire AlarmsIf the sensing threshold of security warnings is set too high, the alarm might not sound in a timely manner, posing a fire hazard.
- Unclassified
Consumer Product Recall · February 12, 2026
Shenzhen Zhongyuantong Technology Co., Ltd., dba SOOWERY of China
SOOWERY 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.
- Class II
Medical Device Recall · February 11, 2026
Burlington Medical, Blockers.Potential for attenuation degradation over time, decreasing the lifespan.
- Class II
Medical Device Recall · February 11, 2026
Burlington Medical, Frontal ApronsPotential for attenuation degradation over time, decreasing the lifespan.
- Class II
Medical Device Recall · February 11, 2026
Burlington Medical, Leg Wraps.Potential for attenuation degradation over time, decreasing the lifespan.
- Class II
Medical Device Recall · February 11, 2026
Waldemar Link GmbH & Co. KG (Mfg Site)
Embrace Drill Tower, Standard/Lateral (25mm); Item Number: 645-081/63;The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described in the surgical technique are correct.
- Class II
Medical Device Recall · February 11, 2026
TMJ Bilateral Implants, REF: CHG020Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided open bite.
- Class I
Food Recall · February 11, 2026
Junebar Chocolate Cherry All Natural Snack Bar; INGREDIENTS: ORGANIC ALMOND BUTTER, DATE PASTE, ORGANIC BLACK BEANS, ORGANIC SWEET POTATOES, GLUTEN FREE ROLLED OATS, SEMI-SWEET SOY FREE VEGAN CHOCOLATProducts contain undeclared milk and soy.
- Class II
Medical Device Recall · February 11, 2026
Burlington Medical, Demi Half Aprons.Potential for attenuation degradation over time, decreasing the lifespan.
- Class II
Medical Device Recall · February 11, 2026
Burlington Medical, KiltPotential for attenuation degradation over time, decreasing the lifespan.
- Class II
Medical Device Recall · February 11, 2026
Burlington Medical, BAT (Breast, Axilla and Thyroid) Coverage.Potential for attenuation degradation over time, decreasing the lifespan.
- Class II
Medical Device Recall · February 11, 2026
Burlington Medical, Kilt Blockers.Potential for attenuation degradation over time, decreasing the lifespan.
- Class II
Medical Device Recall · February 11, 2026
Waldemar Link GmbH & Co. KG (Mfg Site)
Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described in the surgical technique are correct.
- Class II
Medical Device Recall · February 11, 2026
Burlington Medical, Protective Sleeves.Potential for attenuation degradation over time, decreasing the lifespan.
- Class II
Medical Device Recall · February 11, 2026
Burlington Medical, Wrap Aprons.Potential for attenuation degradation over time, decreasing the lifespan.
- Class II
Medical Device Recall · February 11, 2026
Burlington Medical, VestPotential for attenuation degradation over time, decreasing the lifespan.
- Class II
Medical Device Recall · February 11, 2026
Burlington Medical, Caps.Potential for attenuation degradation over time, decreasing the lifespan.
- 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 11, 2026
Burlington Medical, Thyroid Shield.Potential for attenuation degradation over time, decreasing the lifespan.
- 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
BD Alaris" System with Guardrails" Suite MX with Point of Care UnitDue to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi communication with Point-of-Care Units
- 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
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
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)
- 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
Artegraft Vascular Graft; REF#: AG740;Labeling mix-up resulting in the incorrect lot outer packaging of product.
- 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.
- 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)
- 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 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.
- Unclassified
Vehicle Recall · February 7, 2026
2023 KIA TELLURIDE, 2024 KIA TELLURIDEA fire increases the risk of injury.
- Unclassified
Vehicle Recall · February 7, 2026
2023 KIA EV6, 2024 KIA EV6, 2024 KIA EV9A fire increases the risk of injury.
- Unclassified
Vehicle Recall · February 7, 2026
2023 HYUNDAI IONIQ 5, 2024 HYUNDAI IONIQ 5A fire increases the risk of injury.
- 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 Dynamic Matrix Ref: 31057Augmentation devices failed bacterial endotoxin testing.
- 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 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
Vehicle Recall · February 6, 2026
2027 KIA TELLURIDE, 2027 KIA TELLURIDE HYBRIDA seat belt strap that does not extend can fail to restrain an occupant in a crash, increasing the risk of injury.
- 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.