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
34,893 found- Lower riskMedical device
Arrow International Inc recalls Radial Artery Catheterization Set, 1) NA-04550-1A & 2) NA-04550-X1A, device permits access to the peripheral arterial
Arrow recalls two radial artery catheter models due to potential loose polypropylene particles that could cause injury during use. Affected lot numbers: 23F16H0859 and 23F16J0547.
ArrowJul 10, 2017 - Lower riskMedical device
Zimmer Dental Inc recalls IMPLANT,1-PC,ANG,3.0X10MM, REF ZOP30A10; IMPLANT, 1-PC, ANG, 3.0X11.5MM, REF ZOP30A11; IMPLANT, 1 -PC,ANG,3.0X13MM, REF
Zimmer Dental recalls dental implants with missing supplemental instructions. Affected products may not be used safely without proper guides.
Zimmer DentalJul 10, 2017 - Lower riskFood
Texas Legend Foods recalls Silver Star Tex-Mex Style Chipotle Queso Medium Dip Net Wt 16 OZ (1 Lb) packaged in a glass jar
Texas Legend Foods recalls 16oz glass jar quesos with undeclared milk and eggs. Consumers should check lot numbers 060AFV7A, 072AFV7A, : 072AFV7B, 090AFV7A, 111AFV7A for affected products.
Texas Legend FoodsJul 10, 2017 - Stop using nowFood
Reshmi's Group Inc. recalls Sooji Coarse, Siva's brand, packaged in 2 lbs. and 4 lbs poly bags. UPC for 2 lbs. package is 8 46499 00316 1 UPC for 4
Siva's brand Sooji Coarse is recalled due to undeclared wheat. Check your UPCs and consult the remedy for affected packages.
Siva'sJul 10, 2017 - Use cautionVehicle
THOR PALAZZO (2016) recall — Visibility
Thor is recalling 2014-2016 motorhomes where windshield wipers may fail due to incorrect installation, risking reduced driver visibility and crashes.
ThorJul 9, 2017 - Lower riskFood
Sunneen Health Foods, LLC recalls Whole Foods Market PB & J Parfait Made With Greek Yogurt; Net Wt 8 OZ.;
Sunneen Health Foods recalls Whole Foods Market PB & J Parfaits (8 oz) due to misbranded product failing to list soy, almonds, and coconut allergens. Consumers should check labels for correct ingredients.
Sunneen Health FoodsJul 8, 2017 - Use cautionVehicle
DODGE JOURNEY (2015) recall — Air Bags
Chrysler recalls 2011-2015 Dodge Journey vehicles with risk of driver air bag unexpectedly deploying due to wiring harness chafing. Free repairs include wiring replacement and protective cover installation.
ChryslerJul 7, 2017 - Use cautionVehicle
RAM 1500 (2017) recall — Fuel System, Gasoline
Chrysler recalls 2017 Ram 1500 trucks with potentially leaking fuel tanks that could cause fire during rollovers. Owners must have fuel tanks replaced free of charge by dealers.
ChryslerJul 7, 2017 - Use cautionVehicle
JEEP COMPASS (2017) recall — Equipment
Chrysler recalls 2017 Jeep Compass vehicles with incorrect battery jump-start instructions in the User's Guide. Owners must get a corrected guide to avoid injury risks.
ChryslerJul 7, 2017 - Use cautionVehicle
DODGE CHALLENGER (2017) recall — Power Train
Chrysler recalls certain 2017 Dodge Challengers with 5.7L V8 engines and eight-speed automatic transmissions due to potential rolling if exited without parking brake and transmission in PARK.
ChryslerJul 7, 2017 - Lower riskMedical device
Hologic, Inc. recalls Affirm Lateral Arm Upright Biopsy Accessory. Product Number: ASY-09880
Hologic recalls Affirm Lateral Arm Upr: A component issue may affect needle alignment during breast biopsies. No injuries reported. Check product number ASY-09880 for affected units.
HologicJul 7, 2017 - Lower riskMedical device
Amendia, Inc recalls Ceres Self-Drilling Variable Screw 4.0 x 12mm The Ceres screws are self-drilling variable screws that are intended to
Amendia recalls Ceres Self-Drilling Variable Screws 4.0 x 12mm due to incorrect length marking (some screws are 14mm instead of 12mm).
AmendiaJul 7, 2017 - Lower riskMedical device
Ondamed Inc recalls Ondamed Biofeedback Device, Model No. 001-00-0101 The product is a battery powered biofeedback device that is indicated
Ondamed recalls a battery-powered biofeedback device (Model 001-00-0101) sold without FDA marketing clearance. The company has issued an upgrade to improve safety and compliance.
OndamedJul 7, 2017 - Lower riskMedical device
Qualigen Inc recalls Qualigen(R) The FastPack(R) IP Vitamin D Complete Immunoassay Kit, catalog number 25000068 Vitamin D immunoassay kit
Qualigen recalls specific Vitamin D test kits that may give falsely low results. Affected lots: 1701033-3P to 1701033-6P. No remedy stated in official notice.
QualigenJul 7, 2017 - Lower riskMedical device
Amendia, Inc recalls Mac Pin Non-Cannulated Screw, 6.5 x 60mm
Amendia recalls Mac Pin Non-Cannulated Screws (6.5 x 60mm) due to incorrect labeling of pin length. This may cause improper use in medical applications.
AmendiaJul 7, 2017 - Use cautionVehicle
PORSCHE PANAMERA (2012) recall — Engine
Porsche is recalling certain 2010-2012 Panamera models due to camshaft controllers that may come loose, causing engine stalls and crash risks. Owners will receive free replacement fastening screws.
PorscheJul 6, 2017 - Lower riskMedical device
Edwards Lifesciences, LLC recalls Fogarty Adherent Clot Catheter Model Numbers 1408010 and 140806 Product Usage: The Fogarty adherent clot catheters are
Edwards Lifesciences recalls Fogarty Adherent Clot Catheters with 6mm balloon size instead of 10mm. This may cause incomplete clot removal. Affected models 1408010 and 140806.
Edwards LifesciencesJul 6, 2017 - UnratedDrug
Baxter Healthcare Corporation recalls 5% Dextrose Injection, USP, 100 mL VIAFLEX Plastic Container, Rx only, Baxter Healthcare Corporation, Deerfield IL
Baxter Healthcare recalls 100mL 5% Dext: 100mL 5% Dextrose Injection, USP, VIAFLEX Plastic Container (Rx only) due to potential leakage risks. No remedy specified in recall notice.
Baxter HealthcareJul 6, 2017 - UnratedDrug
Hospira Inc., A Pfizer Company recalls Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 5 mL Single-use vial, Rx Only, Sterile, Manufactured by: Gland Pharma
Hospira recalls Argatroban Injection vials with potential impurities that could cause serious health risks. Affected units have specific NDC and lot numbers. Contact Hospira for details.
HospiraJul 6, 2017 - Use cautionDrug
Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP, 250 mL VIAFLEX Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL
Baxter Healthcare recalls 250mL 0.9% Sodium Chloride Injection bags due to leaking containers that could cause infection. Affected units were distributed in Canada with specific product codes.
Baxter HealthcareJul 6, 2017 - Use cautionFood
Innovative Nutrition Technologies recalls BioHealth Pasture Fed Precision Blend Time Release Protein: Cookies and Cream Flavor; Sold in 2 lb.(960G) UPC 6 42014
BioHealth recalls Cookies and Cream protein powder due to undeclared wheat. Check your UPC and lot numbers for details on affected containers.
BioHealthJul 6, 2017 - Lower riskFood
Coborn's, Inc recalls Fudge Brownie, Net Wt. 9 oz. (0.6 lb.) (255g), with the following brands: 1. Cashwise Gluten Free Bakery, 2. Coborn's
Coborn's recalls gluten-free chocolate chip bars labeled as fudge brownies that contain milk. Consumers should check product labels for the correct gluten-free status.
Coborn'sJul 6, 2017 - Use cautionFood
ISABEL NORTH AMERICA, INC. recalls ISABEL, Octopus in vegetable oil, Pulpo en aceite vegetal, Net wt - Peso Neto 4 oz(115g)
Isabel North America recalls Octopus in vegetable oil because the label states octopus but the product contains squid. Check your lot numbers.
IsabelJul 6, 2017 - Stop using nowConsumer product
Cub Cadet Recalls Utility Vehicles Due to Crash Hazard (Recall Alert)
Recalled Cub Cadet 2016 Challenger utility vehicles (model numbers 37AW7CKD010 to 37AY8CND710) have air in brake systems that can cause brake failure and crashes. Consumers must stop using and contact a dealer for free repair.
Cub CadetJul 6, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Persona Partial Knee System, Size 8, Finishing Guide
Zimmer Biomet recalls Persona Partial Knee System Size 8 Finishing Guide due to possible extra surgery time or tightness during knee flexion. Affected units have specific item and lot numbers.
Zimmer BiometJul 5, 2017 - Lower riskMedical device
Teleflex Medical recalls LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600 MADgic, (b) MAD700 MADgic, (c) MAD720
Teleflex Medical recalls LMA MADgic laryngo-tracheal mucosal atomization devices due to potential missing or incomplete package label information. Affected models include MAD600, MAD700, and MAD720 with specific lot numbers.
Teleflex MedicalJul 5, 2017 - Use cautionMedical device
Centurion Medical Products Corporation recalls SafetyGlide Needle, 22GA 1-1/2in, Catalog n. 301701, manufactured by BD, sold in Centurion Convenience Kits. Centurion
Centurion recalls SafetyGlide 22GA 1-1/2in needles (BD catalog 301701) sold in convenience kits from May 2016-June 2017 due to possible particulate expulsion during injection.
CenturionJul 5, 2017 - Use cautionMedical device
Baxter Healthcare Corporation recalls HomeChoice Automated PD system Model numbers: 5C4471, 5C4471R Product Usage: The HomeChoice Automated Personal Cycler
Baxter recalls HomeChoice Automated PD systems (models 5C4471, 5C4471R) due to risk of air delivery into patients if cassettes are damaged during setup. Affected users should check for improper packaging opening.
Baxter HealthcareJul 5, 2017 - Stop using nowMedical device
Orthofix Srl recalls Orthofix Power Drill Torque Limiter, Sterile, Rx Only, Single Use; Sold individually and in the Galaxy UNYCO Diaphyseal
Orthofix recalls power drill torque limiters used in surgery due to potential breakage during procedures. Affected products include specific sterile kits and single-use items sold by Galaxy UNYCO.
OrthofixJul 5, 2017 - Lower riskMedical device
Roche Diagnostics Corporation recalls cobas e 411 Immunoassay Analyzer-Model/Catalog/Part number: 04775279001/04775279973 - cobas e 411 analyzer (disk
Roche recalls cobas e 411 analyzers due to potential software data mismatch. Affected models include specific part numbers. Users should contact Roche for details.
RocheJul 5, 2017
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