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 riskMedical device
TriMed Inc. recalls TriMed Hex Cortical Screw 4.0, 40 mm, REF HEX4.0-40, non-Sterile, RX, a component of the TriMed Ankle Fixation System.
TriMed recalls Hex Cortical Screw 4.0, 40mm (REF HEX4.0-40) due to being shorter than intended. This component of ankle fixation systems may not properly secure fractures during healing.
TriMedAug 24, 2018 - Lower riskMedical device
TriMed Inc. recalls TriMed Dorsal Wrist Hook Plate, Dorsal, 4-Hole, REF WHD-4, contained in a tray, insert, or poly package containing
TriMed recalls Dorsal Wrist Hook Plate model WHD-4 due to potential structural issues from design control process failures. Affected units include specific lot numbers sold in Santa Clarita, CA.
TriMedAug 24, 2018 - UnratedMedical device
Vision RT Ltd recalls Integrated Gate Controller PCB (component of AlignRT Plus) Truebeam variant only. The AlignRT is a video-based
Vision RT recalls specific Integrated Gate Controller PCB components for AlignRT Plus Truebeam systems due to RTInterface errors during I/O communication. Affected units have serial numbers starting with 248- or 249-.
Vision RTAug 24, 2018 - Lower riskMedical device
Life Technologies, Corp. recalls Gibco MEM Non-Essential Amino Acids Solution (100X) (SKU 11140050), for In-Vitro Diagnostic Use
Life Technologies recalls Gibco MEM Non-Essential Amino Acids Solution (100X) for leaky bottles that compromise product sterility. Affected lots expire Dec 2019 and Jan 2020.
Life TechnologiesAug 24, 2018 - Lower riskMedical device
ShinChang Medical Co., Ltd. recalls Disposable Insulin Syringe 0.3mL in 3 different sizes 29Gx1/2, 30Gx5/16, and 31G x 5/16. (10 syringes are packaged in a
ShinChang Medical recalls 0.3mL insulin syringes with small cracks in the barrel that could cause injury during use. Affected products include specific sizes and retailers.
ShinChang MedicalAug 24, 2018 - UnratedDrug
RemedyRepack Inc. recalls Amlodipine/Valsartan HCTZ 10 mg/320 mg/25 mg tablets, HDPE 90 cc bottles in cardboard trays Original NDC 13668-0325-30
RemedyRePack recalls 10 mg/320 mg/25 mg Amlodipine/Valsartan HCTZ tablets in HDPE bottles due to trace NDMA impurity detected in manufacturing.
RemedyRePackAug 24, 2018 - UnratedDrug
Akorn, Inc. recalls Ethosuximide Capsules, USP, 250 mg, 100 capsules per bottle, Rx only, Mfg For VersaPharm Incorporated, Maroerre, GA
Akorn recalls 250 mg Ethosuximide Capsules due to unspecified impurities that may cause harm. Rx-only medication with NDC 61748-025-01, lots 1165280100-1165280101, expiring 3/2019.
AkornAug 24, 2018 - UnratedDrug
Valeant Pharmaceuticals North America LLC recalls Cortaid Intensive Therapy Cooling Spray (1% hydrocortisone), 2 FL OZ (59 mL) spray bottle, OTC, Distributed by: Valeant
Valeant Pharmaceuticals recalls Cortaid Intensive Therapy Cooling Spray (1% hydrocortisone) due to possible microbial contamination from supplier. Check product lot numbers and return unused items.
ValeantAug 24, 2018 - Lower riskDrug
LGM Pharma LLC recalls Thyroid Powder, USP, 25kg/drum, Rx Only, Sichuan Friendly Pharmaceutical Co., LTD. NDC: 070870-1701-1
LGM Pharma recalls Thyroid Powder (25kg drums) due to inconsistent levothyroxine and liothyronine levels. This may affect medication effectiveness. Contact for details.
LGM PharmaAug 24, 2018 - Lower riskFood
Stewart's Shops Corp. recalls Stewart's Ice Cream Caramel Cone Crunch Carton, 1 pint, keep frozen, UPC: 082086444718
Stewart's recalls 1-pint Caramel Cone Crunch ice cream cartons with mislabeled "Crumbs Along the Mohawk" lids. Product must be discarded if the lid is incorrect.
Stewart'sAug 24, 2018 - Lower riskFood
Califia Farms LLC recalls Califia Farms 100% Arabica Coffee; Mocha Cold Brew Coffee with Almond Milk 48 fl. oz. plastic bottle. Dairy Free UPC:
Califia Farms recalls 100% Arabica and Mocha Cold Brew Coffee with Almond Milk 48 fl oz plastic bottles due to potential cleaning chemical contamination from pasteurizer process. Dairy-free products with specific UPCs sold in the US and Canada from November 2018.
Califia FarmsAug 24, 2018 - Use cautionMeat & poultry
Cargill Meat Solutions Recalls Ground Beef Products due to Possible E. coli O157:H7 Contamination
USDA recalls 25,288 pounds of ground beef products from Cargill Meat Solutions due to possible E. coli O157:H7 contamination. Consumers are urged not to consume these products.
Cargill Meat SolutionsAug 23, 2018 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2018) recall — Seats
Daimler Trucks North America recalls 2017-2019 Thomas Built Buses Saf-T-Liner C2 school buses with S3B 45" seats. Seats may detach in crashes, increasing injury risk. Fix: free washer installation by dealers.
Thomas Built BusesAug 23, 2018 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER HDX (2019) recall — Equipment Adaptive/Mobility
Daimler Trucks North America recalls 2019 Thomas Built Buses Saf-T-Liner HDX school buses with certain wheelchair lifts that may tip users inward when exiting, increasing injury risk. Owners must contact DTNA for free cam replacement.
Thomas Built BusesAug 23, 2018 - Use cautionVehicle
RAM 1500 (2019) recall — Power Train
Chrysler recalls certain 2018-2019 RAM 1500 trucks due to potential rear axle failure causing loss of drive or wheel lockup, increasing crash risk. Owners must have rear axle oil inspected and replaced if low.
ChryslerAug 23, 2018 - Use cautionVehicle
MINI COUNTRYMAN (2019) recall — Fuel System, Gasoline
BMW is recalling 2017-2019 MINI Cooper Countryman vehicles that may lack a crash protection plate, risking fuel leaks and fire during crashes. Owners will receive free repairs.
MINIAug 23, 2018 - Use cautionMedical device
Becton Dickinson & Company recalls BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva Catheter), Catalog Number 383539 Product Usage:
Becton Dickinson recalls BD Nexiva Closed IV Catheter System Dual Port 18GA 1.25 IN due to potential needlestick injury risk from a faulty safety mechanism. Affected units include Lot 8087800 with UDI 0130382903835394.
Becton DickinsonAug 23, 2018 - Lower riskMedical device
Stryker Sustainability Solutions recalls Stryker Sustainability Solutions LASSO NAV eco Reprocessed Diagnostic EP Catheters designed to obtain
Stryker recalls eco reprocessed electrophysiology catheters (item # D134903) that are not approved for reprocessing, which could lead to improper use.
Stryker Sustainability SolutionsAug 23, 2018 - Lower riskMedical device
Tosoh Bioscience Inc recalls AIA-360 Analyzer, product code 019945/019945R The Tosoh AIA-360 Automated Immunoassay Analyzer is for use in vitro
Tosoh recalls AIA-360 analyzers due to labeling changes affecting maintenance procedures. Failure to follow new requirements may cause corrosion, contamination, or system failure. Affected units have product code 019945/019945R.
TosohAug 23, 2018 - Stop using nowDrug
Pacific Compounding Pharmacy & Consultations Inc recalls Cefuroxime 10mg/mL INJ 0.5 mg, SDV, Rx only, Pacific Compounding, Stockton, CA
Pacific Compounding Pharmacy recalls Cefuro: Particulate matter in one lot may cause serious reactions. Stop using affected lot numbers immediately.
Pacific CompoundingAug 23, 2018 - Lower riskDrug
Pfizer Global Supply recalls Children s Advil Suspension Ibuprofen Oral Suspension, 100 mg per 5mL, 4 FL OZ (120 ml) bottle, Pfizer, Madison, NJ
Pfizer recalls Children's Advil Suspension due to labeling error causing confusion between teaspoons and milliliters. This may lead to incorrect dosing for children. Affected products have NDC 0573-0207-30.
PfizerAug 23, 2018 - UnratedDrug
LUPIN SOMERSET recalls Morphine Sulfate Extended-Release Tablets, 30 mg, 100-count bottle, Rx only, Manufactured by: Novel Laboratories, Inc.
Lupin Somerset recalls 30mg Morphine Sulfate Extended-Release Tablets (100-count) due to impurity issues found during stability testing. Affected lots may pose health risks.
Lupin SomersetAug 23, 2018 - Lower riskDrug
Hellolife recalls Respitrol, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand
Hellolife recalls Respitrol homeopathic medicine due to microbial contamination. Products may contain harmful bacteria like Staphylococcus saprophyticus and Burkholderia cepacia. Consumers should check product details and contact the company for guidance.
HellolifeAug 23, 2018 - Lower riskFood
Dewey's Bakery, Inc dba Salem Baking Company recalls Dewey's BAKERY Soft Baked TRIPLE CHOCOLATE BROWNIE COOKIES NET WT. 6 OZ paper bag Dewey's BAKERY WINSTON-SALEM, NC
Dewey's Bakery recalls Triple Chocolate Brownie Cookies with mold risk. Stop using if mold is present. Product sold between August 2018 and January 2019.
Dewey's BakeryAug 23, 2018 - Stop using nowConsumer product
Manhattan Toy Recalls Toy Planes Due to Choking Hazard
Manhattan Toy recalls Pull-Back Speedy Jet toy planes due to a choking hazard from separating rubber tires. Check your lot code and return for a refund.
Manhattan ToyAug 23, 2018 - Stop using nowConsumer product
American Landmaster Recalls Off-Road Utility Vehicles Due to Fire and Burn Hazards
American Landmaster recalls 2018 gasoline-powered off-road utility vehicles due to gas tank leaks causing fire and burn risks. Affected models include Landstar, Crossroad, Trailwagon, and others with specific VIN ranges. Consumers must stop using and contact for free repair.
American LandmasterAug 23, 2018 - Use cautionVehicle
NISSAN FRONTIER (2018) recall — Electrical System
Nissan recalls 2018 Frontier vehicles with mechanical key ignition systems that may stall, increasing crash risk. Owners must have ignition switch inspected and replaced if needed.
NissanAug 22, 2018 - Use cautionVehicle
KENWORTH T800 (2018) recall — Engine And Engine Cooling
PACCAR recalls certain 2016-2019 Kenworth T800 trucks with 1.9M ISX15 engines due to potential engine failure without warning. Owners must have harness inspected or replaced free by dealers.
KenworthAug 22, 2018 - Stop using nowMedical device
Smiths Medical ASD Inc. recalls Jelco(R) ViaValve(TM) safety intravenous (I.V.) catheters, 18G x 1 1/4", Model Number REF 3265, MOD 10 The Jelco(R)
Smiths Medical recalls Jelco ViaValve 18G x 1 1/4" I.V. catheters (Model REF 3265, MOD 10) with a V-shaped puncture risk due to manufacturing adjustments. Affected lots include 3584467-3578512. Stop using immediately to prevent injury.
Smiths MedicalAug 22, 2018 - UnratedMedical device
Safe N Simple, LLC recalls Simpurity HYDROGEL ABSORBENT SHEET WOUND DRESSING ADHESIVE BORDER, 4" X 5", 12 Pads, Catalogue number SNS58345
Safe N Simple recalls Simpurity Hydrogel wound dressings with unqualified sterilization. Affected items have catalog number SNS58345 and lot number 18060564. Consumers should check their products for the specific lot number.
Safe N SimpleAug 22, 2018
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