Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
35,069 found- Lower riskMedical device
Becton Dickinson & Company recalls BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a
Becton Dickinson recalls BD Vacutainer Luer Lok Access Devices that may shed contaminants into urine samples, leading to false high red blood cell counts when used with certain analyzers.
Becton DickinsonJan 6, 2022 - Use cautionMedical device
Philips North America recalls Ingenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 989710008732), patient transportation
Philips recalls Ingenia Ambition X patient transport systems with HA FlexTrak II accessory due to potential MRI safety risks from magnetic wheels. Affected units may be attracted to MRI machines if in the magnetic field.
PhilipsJan 6, 2022 - Lower riskFood
World Health Products LLC recalls GAT SPORT JETFUEL DIURETIC; FOR RELIEF OF WATER WEIGHT GAIN; Muscle Defining Formula; Stimulant Free Natural Herbal
World Health Products recalls GAT SPORT JETFUEL DIURETIC supplements due to potential undeclared milk content. Consumers should check lot numbers 2003610 and 2003609 for affected products.
World Health ProductsJan 6, 2022 - Lower riskFood
WayFare Health Foods, LLC. recalls Wayfare Dairy Free Butter Salted & Whipped,
Wayfare Dairy Free Butter Salted & Whipped, recalled due to suspected mold growth before expiration. Check product best by date for affected items.
WayfareJan 6, 2022 - Use cautionFood
Dole Fresh Vegetables Inc recalls Marketside 12oz Classic Salad UPC:6-81131-32894-4 SKU: 3107
Dole recalls Marketside 12oz Classic Salad with Listeria monocytogenes found in harvesting equipment. Consumers should check UPC 6-81131-32894-4 and best by dates from Dec 23, 2021 to Jan 8, 2022.
DoleJan 6, 2022 - Stop using nowConsumer product
Polaris Recalls Youth All-Terrain Vehicles Due to Fire Hazard (Recall Alert)
Polaris recalls certain 2022 Outlaw 110 Youth ATVs due to a fire risk from fuel line leaks. Affected vehicles have specific VINs and color combinations. Owners must stop using and get a free repair.
PolarisJan 6, 2022 - Stop using nowConsumer product
Colony Brands Recalls Children's Wood Wagons Due to Violation of Federal Lead Paint Ban and Lead Poisoning Hazard (Recall Alert)
Colony Brands recalls children's wood wagons with lead paint exceeding safety limits. Excessive lead can cause health issues in young children if ingested. Return wagons for full refund.
Colony BrandsJan 6, 2022 - Use cautionMedical device
Becton Dickinson & Co. recalls BD Veritor Plus Analyzer - intended to provide rapid test results in near-patient settings. Catalog Number: 256066
Becton Dickinson recalls BD Veritor Plus analyzers that may overheat or cause fire if powered by unauthorized AC adapters. Affected units have catalog number 256066 and expire through August 2024.
Becton DickinsonJan 5, 2022 - Lower riskMedical device
DePuy Orthopaedics, Inc. recalls ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Component in total knee arthroplasty (TKA) revision
DePuy recalls ATTUNE revision posterior femoral augment (size 9 12mm) for possible adhesive residue causing soft tissue irritation or infection during knee surgery.
DePuyJan 5, 2022 - Lower riskDrug
Akorn, Inc. recalls Sufentanil Citrate Injection, USP 100 mcg/2 mL (50 mcg/mL) for intravenous and epidural use, Rx only, 2 mL Ampule,
Akorn recalls 2mL Sufentanil Citrate Injection due to subpotent drug levels at 30-month stability. This may affect medical use. Check NDC 17478-0050-02 for affected lots.
AkornJan 5, 2022 - Lower riskDrug
Mylan Pharmaceuticals Inc recalls Semglee (insulin glargine) injection, 100 units/mL (U-100), 3 mL Prefilled Pen (NDC 49502-0196-71), packaged in Five 3
Mylan recalls Semglee (insulin glargine) prefilled pens with missing labels. Check your product's NDC 49502-0196-71 or 49502-0196-75 for affected units. No immediate action needed but label verification is critical for safe use.
MylanJan 5, 2022 - Use cautionConsumer product
Native Creation Recalls Sweaters Due to Violation of the Federal Lead Paint Ban
Native Creation recalls small wool sweaters for children with lead paint on zipper pulls. Excessive lead can cause health issues if ingested by young children. Consumers should stop using and get a refund.
Native CreationJan 5, 2022 - Stop using nowConsumer product
CRT Motor Recalls Youth All-Terrain Vehicles (ATVs) Due to Crash Hazard and Violation of Federal Safety Standard; Sold Exclusively at Motor Planet
CRT Motor recalls youth ATVs (models DF125AVA/DF125AVB) due to crash risk from high speeds and handlebar laceration hazards. Affected vehicles sold exclusively at Motor Planet.
CRT MotorJan 5, 2022 - Use cautionVehicle
AUTOCAR XPEDITOR (2021) recall — Service Brakes, Air
Autocar is recalling 2021-2022 Xpeditor vehicles with incorrect ABS wiring that may increase stopping distance, risking crashes. Owners will receive free repairs by May 30, 2022.
AutocarJan 4, 2022 - Use cautionVehicle
HYUNDAI ACCENT (2020) recall — Seat Belts
Hyundai recalls 2020 Accent vehicles with seat belt pretensioners that may explode in crashes, causing injury. Owners must have the faulty part replaced by dealers.
HyundaiJan 4, 2022 - Lower riskMedical device
Smith & Nephew, Inc. recalls INTEGRA SURFIX ALPHA Screwdriver Torx 10, REF 219 135 ND
Smith & Nephew recalls INTEGRA SURFIX ALPHA Torx 10 screwdrivers that may not properly engage with Surfix Alpha Lock screws, causing potential assembly issues.
Smith & NephewJan 4, 2022 - Use cautionMedical device
BALT USA, LLC recalls The Optima Coil System consists of an implantable embolization coil comprised of a platinum-tungsten alloy attached to
BALT USA recalls Optima Coil System due to incorrect labeling potentially causing wrong coil size selection during procedures, risking vessel damage or aneurysm rupture. Affected units have specific model and lot numbers.
BALT USAJan 4, 2022 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls QC QUALITY CHOICE, Fexofenadine HCl 60mg and Pseudoephedrine HCl 120mg, Extended-Release Tablets, USP, Allergy &
Dr. Reddy's QC QUALITY CHOICE extended-release allergy tablets with failed dissolution specifications are recalled. Consumers should check NDC 63868-729-10 and lot numbers 79C002624D/79C002625C.
Dr. Reddy'sJan 4, 2022 - Lower riskMedical device
Immuno-Mycologics, Inc recalls CRYPTOCOCCAL ANTIGEN LATERAL FLOW ASSAY, IMMY, Lateral Flow Assay for the Detection of Cryptococcal Antigen in serum
Immuno-Mycologics recalls IMMY Cryptococcal Antigen Lateral Flow Assay due to reduced specificity causing false positives. Affected tests may lead to unnecessary anti-fungal treatment. No action needed for negative results.
Immuno-MycologicsJan 3, 2022 - UnratedMedical device
Philips North America Llc recalls eCareManager version 4.2.1, eCareManager version 4.3.2, eCareManager version 4.3.3, eCareManager version 4.5.1,
Philips recalls specific versions of eCareManager software for in-hospital patient care. The unapproved software may not be safe for medical use. Affected units include model 865325 with listed software versions.
PhilipsJan 3, 2022 - Lower riskFood
SWAP FOODS LLC recalls Everything Swapples, Net Wt. 11.14 OZ, UPC 8 64390 00021 3
SWAP FOODS LLC recalls Everything Swapples (11.14 oz) due to potential plastic contamination. Consumers should check UPC 8 64390 00021 3 and lot numbers for affected products.
SWAP FOODSJan 3, 2022 - Stop using nowVehicle
JAYCO NORTHPOINT (2021) recall — Tires
Jayco recalls 2021-2022 NorthPoint trailers with specific Sailun tires due to potential belt separation causing loss of vehicle control. Affected tires have DOT code 1YJ and date code 2020-4120.
JaycoJan 2, 2022 - Use cautionVehicle
TESLA MODEL 3 (2020) recall — Electrical System
Tesla is recalling 2020 Model 3 vehicles due to potential seat belt unawareness during crashes. This affects safety compliance with federal standards. Owners must update software to prevent injury risks.
TeslaJan 2, 2022 - Lower riskFood
Renaissance Food Group, LLC recalls CHICKEN SALAD Croissant NET WT. 7.8OZ (221g) Perishable, Keep Refrigerated Ingredients: Chicken Salad***Savory
Renaissance Food Group recalls Chicken Salad Croissant (7.8oz) due to unlabeled tuna salad ingredient. Products sold between January 2022 and present may contain fish without declaration.
Renaissance Food GroupJan 2, 2022 - Use cautionVehicle
ROSENBAUER COMMANDER (2018) recall — Fuel System, Diesel
Rosenbauer recalls 2018-2022 Commander and Warrior trucks with potential diesel fuel leaks that could cause fire if near ignition sources. Owners must contact Cummins for free repairs.
RosenbauerJan 1, 2022 - UnratedDrug
Rubicon Research Private Limited recalls Metoprolol Tartrate Tablets, USP 25 mg, 1000 - count bottle, Rx Only, Distributed by: TruPharma, LLC. Tampa, FL 33609;
Rubicon Research recalls 25mg Metoprolol Tartrate tablets due to metal foreign matter. Rx-only bottles distributed by TruPharma. No remedy stated in official notice.
Rubicon ResearchDec 31, 2021 - UnratedDrug
Teva Pharmaceuticals USA recalls MethylPREDNISolone Acetate Injectable Suspension USP 400 mg/10mL (40mg/mL), 10 mL Multiple-Dose Vial, Rx Only,
Teva Pharmaceuticals USA recalls 10mL multiple-dose vials of Methylprednisolone Acetate Injectable Suspension due to lack of sterility assurance. This could lead to infections if used improperly.
Teva Pharmaceuticals USADec 31, 2021 - Use cautionFood
Organic By Nature, Inc. recalls Purim Health Brands EpiGenius Kids Chocolate: Daily Superfood 630 g pouches Suggested Use: Mix approximately three
Organic By Nature recalls EpiGenius Kids Chocolate pouches with undeclared milk. Consumers should check product numbers and lots for affected items.
Organic By NatureDec 31, 2021 - UnratedMedical device
RAYSEARCH LABORATORIES AB recalls RayStation/RayPlan- designed for treatment planning and analysis of radiation therapy. Software Version: 6.0.0.24 ,
RaySearch recalls specific versions of RayStation/RayPlan software due to display errors when new images are selected during cine loops. Affected versions include 6.0.0.24 through 9.2.0.483. No remedy is stated in the recall notice.
RaySearchDec 30, 2021 - Lower riskMedical device
Howmedica Osteonics Corp. recalls Exeter V40 Cemented Hip (150mm) Stem, Part Number 0580-1-440
Howmedica recalls Exeter V40 Cemented Hip (150mm) Stem (Part 0580-1-440) due to potential label mix with 125mm stem. Affected units may be used incorrectly.
HowmedicaDec 30, 2021
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