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
34,943 found- Lower riskDrug
Akorn, Inc. recalls Lidocaine 2.5% and Prilocaine Cream, 2.5%. 30g tube, Rx only, Manufactured by: Hi-Tech Pharmacal Co., Inc., Amityville,
Akorn recalls Lidocaine 2.5% and Prilocaine 2. 5% 30g tubes (Rx only) due to stability testing finding an unknown impurity that may degrade the product.
AkornAug 1, 2018 - Lower riskDrug
Baxter Healthcare Corporation recalls Levofloxacin Injection in 5% Dextrose, 250 mg (5 mg/mL), 250 mg in 50 mL 5% Dextrose, 50 mL Single Use Container bag,
Baxter Healthcare recalls specific levofloxacin injection products due to high drug concentration risks. This affects certain lots manufactured in 2018-2019. Contact for details.
Baxter HealthcareAug 1, 2018 - Lower riskFood
HP Hood LLC recalls Blue Diamond Almond Breeze Almond Milk, Half Gallon
HP Hood recalls Blue Diamond Almond Breeze Almond Milk due to testing positive for milk allergen. Consumers should check product codes and contact HP Hood for details.
HP HoodAug 1, 2018 - Stop using nowFood
Dole Fresh Vegetables Inc recalls Dole Classic Coleslaw, 14 oz. (397 g) plastic bag; Green Cabbage, shredded carrots. UPC Code 7143001066 Distributed by
Dole Fresh Vegetables recalls limited quantities of Classic Coleslaw due to potential metal fragments. Check your UPC and codes.
DoleAug 1, 2018 - Lower riskFood
Sweet Earth Inc. recalls Sweet Earth Foods Aloha BBQ Quesadilla; 2 pack, NET WT 8 oz. Vegan: Pinto Beans, Red Onions, Pineapple and jalapenos
Sweet Earth recalls 2-pack vegan BBQ quesadillas due to missing egg and milk declarations on packaging. Consumers should check for the UPC 016741000551 label.
Sweet EarthAug 1, 2018 - Lower riskFood
Artashes LLC recalls Ararat Imambayeldy; 18.3 oz. glass jar; Ingredient: Eggplant, tomato paste, onions, vegetable oil, garlic, green salt
FDA foreign inspection found pH levels in Ararat Imambayeldy 18.3 oz glass jars to be above scheduled process. Consumers should check batch numbers on jars for affected products.
Ararat ImambayeldyAug 1, 2018 - Use cautionConsumer product
BMC Recalls Bicycles Due to Fall Hazard
BMC recalls 2017-2018 Timemachine 01 road bikes due to risk of falls from insufficient front wheel clearance. Consumers must stop using and get a free fork inspection or replacement by September/October 2018.
BMCAug 1, 2018 - Use cautionVehicle
FREIGHTLINER CASCADIA (2015) recall — Steering
Daimler Trucks North America recalls 2012-2015 Freightliner Cascadia trucks with potential tie-rod tube failure causing loss of steering. Free replacement of brake linings, brake spider, and tie-rod available.
Daimler Trucks North AmericaJul 31, 2018 - Use cautionVehicle
HEARTLAND SUNDANCE XLT TT (2018) recall — Tires
Heartland is recalling 2018 Sundance XLT TT trailers with incorrect Load Range C tires that could fail under overload, risking crashes. Owners get free tire replacements.
HeartlandJul 31, 2018 - Lower riskMedical device
Endologix recalls ENDOLOGIX AFX/AFX2, Proximal (Aortic) Extension Endograft, Rx Only, Sterile EO, AFX Proximal Accessory, Infrarenal
Endologix recalls specific AFX/AFX2 endograft models due to potential Type III endoleaks requiring patient surveillance. This follow-up notification addresses updated monitoring recommendations.
EndologixJul 31, 2018 - Use cautionMedical device
Oridion Medical 1987 Ltd. recalls Capnostream20 M ADULT ICU (CPM), CS08654RA
Oridion Medical recalls Capnostream20 M adult ICU monitors (CS08654RA) due to potential reset of alarm settings when powered off. Affected units may require reconfiguration.
Oridion MedicalJul 31, 2018 - Use cautionConsumer product
Additional Incidents Prompt Johnson Health Tech to Reannounce Recall of Matrix Fitness Ascent Trainers and Ellipticals Due to Fire Hazard (Recall Alert)
Matrix recalls Ascent trainers and ellipticals from 2011-2012 due to moisture causing short circuits and fire risks. Affected units have specific model numbers and serial codes. Contact for free repair.
MatrixJul 31, 2018 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Beef, Pork and Poultry Salad and Wrap Products due to Concerns about Contamination with Cyclospora
U.S. Department of Agriculture recalls beef, pork and poultry salad and wrap products from Caito Foods LLC due to potential Cyclospora contamination. Consumers are urged not to consume these items.
Caito FoodsJul 30, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Zimmer Natural Nail Tibial Nail - Yellow 8.3mm, Model Number 47249534008 Product Usage - The Zimmer Natural Nail System
Zimmer Biomet recalls Yellow 8.3mm Tibial Nails (Model 47249534008) that are actually 12mm. This size error may cause improper bone fixation during fracture treatment.
Zimmer BiometJul 30, 2018 - Lower riskMedical device
Arrow International Inc recalls ARROW¿ Bipolar Electrode Catheter with shrouded pins , 6 Fr, 110 cm Product Code: AI-06210-S Product Usage: Arrow
Arrow recalls bipolar electrode catheters with incorrect expiration dates. Products labeled with wrong use-by date may expire before intended use. Consumers should check product labels for correct expiration date.
ArrowJul 30, 2018 - Use cautionMedical device
Civco Medical Instruments Co. Inc. recalls CIVCO Needle Guide, REF 676-150, QTY 24, STERILE EO
Civco recalls 24 sterile needle guides (REF 676-150) due to missing or weak adhesive causing assembly failure. Affected units have specific lot numbers and UDI.
CivcoJul 30, 2018 - Use cautionMedical device
Zimmer Biomet Spine Inc. recalls Vitality¿ Spinal Fixation System.Spinal Intervertebral Body, Appliance, Fixation (non-sterile). Pedicle screw fixation
Zimmer Biomet recalls certain Vitality Spinal Fixation System screws due to improper threading that could cause device failure during spinal fusion surgery.
Zimmer BiometJul 30, 2018 - Lower riskMedical device
Beckman Coulter Inc. recalls UniCel DxH 800 Coulter Cellular Analysis System, REF numbers 629029, B24465, B24802, B68304, B66445, and B63322.
Beckman Coulter recalls UniCel DxH 800 analyzers with specific serial numbers due to sporadic platelet errors that could lead to unrecognized low platelet counts, potentially causing health risks.
Beckman Coul: 1-2 wordsJul 30, 2018 - Lower riskDrug
MAJOR PHARMACEUTICALS recalls Doxycycline Hyclate Tablets, USP, 100 mg, Rx Only, 30 tablets, 3 x 10 unit dose Cartons, Mfd. by: West-Ward
Major Pharmaceuticals is recalling 100 mg Doxycycline Hyclate Tablets due to failed dissolution specifications. This may affect medication effectiveness. Contact for details.
Major PharmaceuticalsJul 30, 2018 - UnratedDrug
NuCare Pharmaceuticals Inc recalls Valsartan/HCTZ 320/25mg Tablets, 30-count jar, Rx Only, Packaged by NuCare Pharmaceuticals, Inc., Orange, CA 92867, NDC
NuCare Pharmaceuticals recalls 320/25mg Valsartan/HCTZ tablets due to detected carcinogen impurity in manufacturing. This may pose cancer risk. Check your prescription label for NDC 68071-4183-3.
NuCare PharmaceuticalsJul 30, 2018 - Lower riskFood
Driscoll's Strawberry Associates, Inc. recalls Driscoll's Only the Finest Berries; Strawberries Fraises; NET WT 16 oz. (1 lb.) Product of the USA Driscoll Strawberry
Driscoll's recalls 16oz strawberries due to potential blood contamination. Consumers should check for the specific lot code and contact Driscoll's for details.
Driscoll'sJul 30, 2018 - Stop using nowFood
Caito Foods LLC. recalls Delish Vegetable Garden Salad, 10.5 oz. UPC 49022542426
Caito Foods LLC recalls Delish Vegetable Garden Salad (10.5 oz) due to potential Cyclospora contamination. Check your UPC and enjoy-by dates.
DelishJul 30, 2018 - Use cautionVehicle
MERCEDES-BENZ METRIS (2018) recall — Power Train
Daimler Vans USA recalls 2017-2018 Mercedes-Benz Metris vehicles with potential driveshaft separation causing crash risk. Free transmission flange repair available.
Mercedes-BenzJul 29, 2018 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model Number 10849000
Siemens recalls ARTIS Pheno Interventional Fluoroscopic X-Ray System (Model 10849000) due to potential temperature control failure when unpowered for long periods.
SiemensJul 29, 2018 - Use cautionVehicle
RAM 1500 (2017) recall — Structure
Chrysler is recalling certain 2015-2017 RAM 1500 trucks with power tailgates that may unlatch while driving, risking cargo falling out and crashes. Owners must contact customer service for free repairs.
ChryslerJul 27, 2018 - Stop using nowVehicle
GENESIS G80 (2018) recall — Air Bags
Hyundai is recalling 2018 Genesis G80 vehicles because the passenger air bag may deploy even if a child is in the seat. Check recall number 002G.
GenesisJul 27, 2018 - Lower riskMedical device
Sysmex America, Inc. recalls Sysmex XN-Series Fluorocell PLT, Catalog #CD994563. Distributed in the U.S.A. by Sysmex America, Inc., Lincolnshire,
Sysmex recalls XN-Series Fluorocell PLT reagents that may show falsely low platelet counts, affecting blood test accuracy. Affected lots have specific expiration dates.
SysmexJul 27, 2018 - Lower riskMedical device
Synvasive Technology Inc recalls ZIMMER Oscillating Saw Blade -Cutting 75mm x 19mm x 1.00/1.27mm.intended for bone or cartilage in orthopedic
Synvasive recalls Zimmer oscillating saw blades with mislabeled width (19mm actual vs 25mm on label) for orthopedic use. Affected blades may cause incorrect cutting if used with wrong specifications.
SynvasiveJul 27, 2018 - Lower riskMedical device
Stryker Sustainability Solutions recalls Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut
Stryker Sustainability Solutions recalls reprocessed arthroscopic shavers with specific catalog numbers that may display incorrect settings or error messages when connected to generators, potentially affecting surgical use.
Stryker Sustainability SolutionsJul 27, 2018 - UnratedDrug
Bryant Ranch Prepack Inc. recalls Valsartan 80 mg tablets, 90-count bottles (NDC 63629-6922-2), 60-count bottles ( 63629-6922-3), 28-count bottles
Bryant Ranch Prepack Inc. recalls Valsartan 80 mg tablets due to detected carcinogen impurity in manufacturing. Affected lots include specific NDC numbers and expiration dates. Consumers should contact the manufacturer for details.
Bryant RanchJul 27, 2018
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