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 riskFood
Subco Foods Inc. recalls Only 8 Vanilla Yogurt 2.8 pound pouch 6 pouches per case
Subco Foods recalls 8-pouch vanilla yogurt due to potential salmonella contamination in whey used for production. Consumers should avoid these products to prevent foodborne illness.
Subco FoodsJul 18, 2018 - Stop using nowFood
H-E-B GROCERY COMPANY LP DBA HEB recalls HEB Creamy Creations Vanilla Chocolate Cup 3 oz packaged in a 12 count plastic bag - (6-3oz. Chocolate Ice Cream cups
H-E-B is recalling specific lots of Creamy Creations Vanilla Chocolate Cups due to potential metal fragments. Check your UPC and code date.
H-E-BJul 18, 2018 - Lower riskFood
FLOWERS FOODS recalls Swiss Rolls***Brand Name**Swiss Rolls Chocolate (Snack) Cakes, NET WT OZ (g) PKGS***TWIN PACKS***Nutrition
Flowers Foods recalls Swiss Rolls chocolate cakes due to potential salmonella in whey powder. Products sold under multiple brand names with specific UPCs and best-by dates are affected. Consumers should check their packages for the listed UPCs and dates.
Flowers FoodsJul 18, 2018 - Lower riskFood
Advanced Food Concepts recalls GU Energy Gels: Caramel Macchiato, Gel; GUGEL 1 Pkt; item # 123031, UPC 769493200518; GUGEL 24Pkt Box; item number
Advanced Food Concepts recalls GU Energy Gels (Caramel Macchiato, Gel) due to potential cyclamate contamination. All affected products should be checked for the listed UPCs and item numbers.
Advanced Food ConceptsJul 18, 2018 - Stop using nowConsumer product
Crate and Barrel Recalls Mirrors Due to Laceration Hazard (Recall Alert)
Crate and Barrel recalls Josephine floor mirrors due to risk of glass separating from wooden backing and causing lacerations. Consumers should stop using and return for free replacement.
Crate and BarrelJul 18, 2018 - Use cautionMeat & poultry
Smithfield Packaged Meats Corp. Recalls Pepperoni Five Cheese Calzone Products Due to Possible Extraneous Material Contamination
Smithfield recalls pepperoni five cheese calzones from May 2018 due to possible sharp plastic pieces. Consumers should not eat these products and dispose of them safely.
SmithfieldJul 17, 2018 - Use cautionVehicle
BMW M5 (2018) recall — Fuel System, Gasoline
BMW recalls 2018 M5 vehicles with potential fuel gauge inaccuracies that could cause stalling and increase crash risk. Owners must have fuel line secured by dealers.
BMWJul 17, 2018 - Lower riskMedical device
Abbott Laboratories, Inc recalls Abbott ARCHITECT c4000 Processing Module, List No. 02P24 - Product Usage: The Abbott ARCHITECT System is intended for
Abbott recalls ARCHITECT c4000 Processing Module (List No. 02P24) due to potential incorrect test results if error codes aren't resolved before running tests. Affected units may need correction to ensure accurate diagnostic results.
AbbottJul 17, 2018 - Use cautionMedical device
Alcon Research Laboratories Ltd. recalls Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic
Alcon recalls LuxOr E71 and E71 Q-Vue ophthalmic microscopes with potential optical head detachment due to thread adhesive. Affected units have specific US serial numbers listed in the recall notice.
AlconJul 17, 2018 - Lower riskMedical device
Arrow International Inc recalls 4.5 Fr x 40 cm single-lumen PICC Kit, Product Code CDC-44041-VPS2, 5.5 Fr double-lumen PICC Kit, Product Code
Arrow recalls two PICC kits that may contain incorrect catheter sizes, risking treatment delays. Affected kits have specific product codes and were sold in the U.S. Learn how to check and what to do.
ArrowJul 17, 2018 - Use cautionMedical device
Liko AB recalls Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.
Liko recalls Multirall 200 Strap Gripper (P/N 3136250) made on May 5, 2017, due to potential patient falls from incorrect assembly during patient transfers.
LikoJul 17, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 440 mm, Item Number: 814309440
Zimmer Biomet recalls specific hip fracture nail models due to set screw failure. Affected items may not advance or reverse properly, potentially causing improper fixation.
Zimmer BiometJul 17, 2018 - UnratedDrug
Longbow First Aid Products Manufactory recalls Emergency First Aid Eyewash (Purified Water 98.3%), packaged in a) 4fl oz. (118 ml) NDC 7110500002, and b) 0.67 fl (20
Longbow recalls emergency eyewash bottles with CGMP deviations. These purified water products may have quality issues affecting safety. Consumers should check product labels for NDC 7110500002 or 71150000.
Longbow First Aid ProductsJul 17, 2018 - UnratedDrug
A-S Medication Solutions LLC. recalls Valsartan and Hydrochlorothiazide Tablets, Valsartan 320 MG and Hydrochlorothiazide 25 MG, 90 tablets per bottle, Rx
A-S Medication Solutions recalls Valsartan 320mg and Hydrochlorothiazide 25mg tablets due to detected carcinogen impurity in manufacturing. Affected lots from 2018-2019.
A-S Medication SolutionsJul 17, 2018 - UnratedDrug
RemedyRepack Inc. recalls Valsartan/HCTZ 320mg/12.5 mg tablet, 90-count bottle, Rx only, RemedyRepack, 625 Kolter Drive, Suite 4, Indiana, PA
RemedyRepack recalls 320mg/12.5mg Valsartan/HCT: Carcinogen impurity detected in manufacturing. Rx-only tablets with lot # B0383153-122917. Contact for return instructions.
RemedyRepackJul 17, 2018 - Lower riskFood
Country Fresh Food & Confections Inc. recalls Cracker Barrel OLD FASHIONED COUNTRY CANDIES KETTLE COOKED FUDGE PEANUT BUTTER, Nutrition Facts***INGREDIENTS: SUGAR,
Cracker Barrel recalls fudge peanut butter products due to incorrect ingredient labeling. Products may contain undeclared peanut butter, posing a risk for allergic individuals. Check packaging for specific batch numbers and contact Cracker Barrel for details.
Cracker BarrelJul 17, 2018 - Stop using nowFood
Portland French Bakery L T D recalls Seattle Sourdough Pub Buns 6 pack, net wt. 16 oz., UPC 0-72220-10164-5
Portland French Bakery recalls Seattle Sourdough Pub Buns 6 pack due to undeclared soy. Check your UPC and best before dates.
Seattle SourdoughJul 17, 2018 - Lower riskFood
Innova Flavours recalls Natural Roasted Garlic Herb Flavor, 40 pounds, Powder in a blue poly-lined cardboard box, Ambient
Innova Flavours is recalling Natural Roasted Garlic Herb Flavor powder due to potential Salmonella contamination from a supplier's recalled sweet whey powder. Consumers should avoid using this product until further notice.
Innova FlavoursJul 17, 2018 - Lower riskFood
Holmquist Hazelnut Orchards recalls Butter Toffee Flavored Hazelnuts, packaged in a clear plastic bag, net wt 6 oz. UPC 7 39059 30612 1. The label is read
Holmquist Hazelnut Orchards recalls Butter Toffee Flavored Hazelnuts due to milk not being declared on the label, which may cause allergic reactions in people with dairy allergies.
Holmquist Hazelnut OrchardsJul 17, 2018 - Lower riskFood
Griffith Labs U.S.A. recalls Caesar Seasoning 50 pound bag Item 1000031193
Griffith Labs recalls 50-pound Caesar Seasoning bags (item 1000031193) due to potential Salmonella contamination from recalled whey ingredient. Consumers should check batch numbers 673826, 676245, or 676986 for affected products.
Griffith LabsJul 17, 2018 - Use cautionMeat & poultry
New Seasons Market Recalls Ready-To-Eat Sesame Noodle Chicken Salad Products Due to Misbranding and Undeclared Allergens
New Seasons Market recalls ready-to-eat sesame noodle chicken salad products containing undeclared peanuts. Consumers are urged not to consume these products and should discard or return them.
New Seasons MarketJul 16, 2018 - Use cautionVehicle
FORD FUSION (2016) recall — Power Train
Ford is recalling 2016 Fusion vehicles with a power train issue that may cause unintended vehicle movement when exiting without parking brake and transmission in Park.
FordJul 16, 2018 - Use cautionVehicle
FORD F53 (2018) recall — Wheels
Ford recalls 2018 F53 trucks with potentially unsafe wheel studs that could lead to handling issues and crashes. Owners must contact Ford for free hub stud replacement.
FordJul 16, 2018 - Lower riskMedical device
In2bones USA, LLC recalls CoLink(TM) Lapidus Plate XP, +2 mm, Right, REF P40 ST165, QTY 1, In2Bones Product Usage: The In2Bones USA LLC, CoLink¿
In2bones recalls one unit of CoLink Lapidus Plate XP +2mm Right (REF P40 ST1:165) due to incorrect laser marking. This could lead to improper use in orthopedic procedures.
In2bonesJul 16, 2018 - Lower riskMedical device
Valeris Medical, LLC recalls Valeris Medical Apollo Medial Suture Anchor, Catalog Number MSA-4515, 4.5 x 15mm, each package contains (1) PEEK Screw,
Valeris Medical recalls Apollo Medial Suture Anchor (MSA-4515) due to mislabeling with incorrect suture type. Affected units contain 5 packages per container, sterile, Rx only.
Valeris MedicalJul 16, 2018 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci Si/X/Xi Surgical System Redundant Medical Grade Power Supply (RMGPS) Units The da Vinci System consists of a
Intuitive Surgical recalls specific Redundant Medical Grade Power Supply (RMGPS) units for da Vinci Si/X/Xi Surgical Systems due to potential failure during use, which could disrupt surgery. Affected units have model numbers listed in the recall notice.
Intuitive SurgicalJul 16, 2018 - Lower riskMedical device
Roche Diagnostics Corporation recalls Roche cobas p 612 pre-analytical system (63x) Model: 07563116001 The cobas p 612 pre-analytical system is a computer
Roche recalls cobas p 612 pre-analytical systems (model 07563116001) due to potential contamination causing false positive test results. All units are affected.
RocheJul 16, 2018 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls RAPIDLab 1265 Blood Gas Analyzer; 110321852, 10470366, 10491395 Device is point-of-care system for comprehensive
Siemens Healthcare recalls RAPIDLab 1265 Blood Gas Analyzers with serial numbers 110321852, 10470366, 10491395 due to potential hydroxocobalamin interference causing inaccurate blood gas readings, which could affect patient treatment decisions.
Siemens HealthcareJul 16, 2018 - Stop using nowMedical device
Philips Electronics North America Corporation recalls AIIuraXperFDlO/10, System Code 722011 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging
Philips recalls certain cardiac imaging monitors from 2003-2011 that may detach and fall, risking injury. Affected units have System Code 722011. Stop using immediately if you own one.
PhilipsJul 16, 2018 - UnratedDrug
Teva Pharmaceuticals USA recalls Omega-3-Acid Ethyl Esters Capsules USP, 1 gram* 120-count bottle Rx Only. Manufactured by: Banner Pharmacaps, Inc. High
Teva Pharmaceuticals USA recalls 120-count Omega-3 capsules due to unapproved manufacturing materials. This may pose safety risks if taken without regulatory approval. Consumers should contact Teva for details.
Teva Pharmaceuticals USAJul 16, 2018
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