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- Stop using nowDrug
Chiavna Saffron LLC recalls Super Panther 7K Capsules 1250 mg blend, a) 1 count blister cards shipped in boxes of 30 (UPC# 6015577513247); and b) 6
FDA recalls Super Panther 7K Capsules 1250 mg blend due to contamination with sildendafil and tadalafil. Consumers should not use these products as they pose health risks.
Chiavna SaffronJul 21, 2017 - Use cautionFood
Duy Drugs Inc. recalls Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
Duy Drugs Inc. recalls Cardiovid Plus dietary supplements because they may not meet federal quality standards for identity, purity, and composition.
Duy DrugsJul 21, 2017 - Lower riskFood
GRANDE PRODUCE LTD CO recalls Caribena yellow maradol papaya packed in 35 pound cases
Grande Produce recalls yellow maradol papaya in 35-pound cases due to Salmonella contamination. Consumers should avoid these products to prevent foodborne illness.
Grande ProduceJul 21, 2017 - Lower riskFood
Professional Complementary Health Formulas, LLC recalls Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in white plastic
Professional Formulas recalls Sublinqual B12 High-Potency supplements due to lactose in ingredients not listed on label. Affected products include 60-count dissolvable tablets with specific lot numbers and QR codes.
Professional FormulasJul 21, 2017 - Use cautionFood
Bush Brothers & Co recalls BUSHS BEST¿ Country Style THICK, RICH SAUCE WITH BACON & EXTRA BROWN SUGAR 28 OZ (1 LB 12 OZ) 794 g BUSH BROTHERS &
Bush Brothers recalls 28oz Country Style Thick Sauce with Bacon & Brown Sugar due to potential C. botulinum growth from leaking cans. Consumers should check lot codes and contact the company for details.
Bush BrothersJul 21, 2017 - Lower riskFood
Koogee-Queen Anne, LLC recalls The Comfy Cow Salted Caramel Ice Cream 1 pint
Koogee-Queen Anne recalls Salted Caramel Ice Cream due to E. coli and high Coliform Bacteria counts. Consumers should check product lot numbers and avoid consumption.
Koogee-Queen AnneJul 21, 2017 - Stop using nowConsumer product
ZORJAR Recalls Women's Scarves Due to Violation of Federal Flammability Standard; Sold Exclusively on Amazon.com (Recall Alert)
ZORJAR women's silk scarves sold on Amazon fail federal flammability standards, risking burns. Consumers must stop using and get refunds.
ZORJARJul 21, 2017 - Lower riskMeat & poultry
Cesina Sausage Company Recalls Pork Product Due To Misbranding
USDA recalls Cesina pork kolbassi due to mislabeled ready-to-eat status. Consumers urged not to eat recalled product.
CesinaJul 20, 2017 - Use cautionVehicle
MITSUBISHI OUTLANDER (2013) recall — Visibility
Mitsubishi recalls 2013 Outlander vehicles with wiper motor failure risk due to water leakage causing corrosion. Owners must have wiper motor replaced free by dealers.
MitsubishiJul 20, 2017 - Use cautionVehicle
TOYOTA AVALON HYBRID (2016) recall — Power Train
Toyota recalls 2016 Avalon Hybrid vehicles with potential front drive shaft separation causing loss of propulsion and rolling risk if driver exits without parking brake.
ToyotaJul 20, 2017 - Lower riskMedical device
Beckman Coulter Inc. recalls Sekisui Diagnostics Sekure Chemistry Acetaminophen L3K , Ref. 506-30. The firm names on the label are Sekisui
Sekisui Diagnostics recalls acetaminophen L3K reagents due to potential false lipase results in lab tests. Affected units include all lots of Sekure Chemistry Acetaminophen L3K Ref. 506-30.
Sekisui DiagnosticsJul 20, 2017 - UnratedDrug
Hetero USA Inc recalls Entecavir Tablets 0.5 mg, 30 tablets per container, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc.,
Hetero USA recalls Entecav: 0.5mg tablets with impurity levels exceeding safety limits. This drug may have unsafe chemical levels that could affect health. Consumers should contact the manufacturer for details.
Hetero USAJul 20, 2017 - Lower riskFood
Grandma's Herbs recalls "Because They Work" GRANDMA'S HERBS CHOLESTEROL SUPPORT, Dietary Supplement, 100 Capsules 480 mg. Packaging: PET
Grandma's Herbs recalls 100-capsule cholesterol support supplements due to undeclared soy lecithin. Consumers should check product details and contact the company for guidance.
Grandma's HerbsJul 20, 2017 - Stop using nowConsumer product
Manhattan Toy Recalls Activity Toys Due to Choking Hazard
Winkel Colorburst activity toys with specific lot codes recalled due to choking hazard from brittle plastic tubes. Consumers should stop using and return toys for refund.
WinkelJul 20, 2017 - Use cautionMedical device
Genicon, Inc. recalls GENICON EZEE Retrieval, sterile, Rx only.
Genicon recalls sterile EZEE Retrieval devices due to plastic handle breaking off, which can prevent proper removal. Affected units have specific catalog and lot numbers.
GeniconJul 19, 2017 - Lower riskMedical device
Kamiya Biomedical Company, LLC recalls K-Assay(R) Multi-Analyte Calibrator, REF KAI--016C, KAMIYA BIOMEDICAL COMPANY, Seattle, WA, IVD The K-ASSAY(R)
Kamiya recalls specific lots of K-Assay Multi-Analyte Calibrator due to incorrect AlAT calibrator values in package inserts, potentially affecting lab test accuracy.
KamiyaJul 19, 2017 - Use cautionMedical device
Teleflex Medical recalls Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means
Teleflex Medical recalls Percuvance Maryland Dissector Tool Tips with 5mm attachments due to potential connection compromise or abrupt jaw closure during laparoscopic surgery.
Teleflex MedicalJul 19, 2017 - UnratedDrug
AVKARE Inc. recalls Voriconazole Tablets, 200 mg, 20-count cartons (4 x 5) Unit Dose, Rx only, Manufactured for: AvKARE, Inc. Pulaski, TN
AvKARE recalls specific lots of Voriconazole Tablets 200 mg because they failed impurity specifications. Check your lot numbers and expiration dates for details.
AvKAREJul 19, 2017 - Lower riskFood
General Mills, Inc recalls IQF White Rice ES CA, Cardboard Tote, product #4621686100.
General Mills recalls IQF White Rice ES CA (product #4621686100) due to potential egg and wheat contamination. Consumers should check packaging for the specific product code.
General MillsJul 19, 2017 - Stop using nowFood
TRULY GOOD FOODS recalls Pumpkin Seeds, Blackened Seasoned 10 LB
Truly Good Foods recalls 10lb Blackened Seasoned Pumpkin Seeds due to accidental mixing with tree nuts (almonds, cashews). Consumers should avoid these products to prevent allergic reactions.
Truly Good FoodsJul 19, 2017 - Stop using nowConsumer product
Polaris Recalls Sportsman 570 All-Terrain Vehicles Due to Fuel Leak, Fire Hazards
Polaris recalls 2014 Sportsman 570 ATVs due to fuel leaks in headlight pods that could cause fires. Affected models include Sage Green, Indy Red, and Polaris Pursuit Camo versions. Consumers must stop using and contact Polaris for free repairs.
PolarisJul 19, 2017 - Stop using nowVehicle
MAZDA MAZDA6 (2012) recall — Air Bags
Mazda recalls 2012 Mazda6 vehicles with potential air bag inflator rupture causing serious injury or death. Owners must stop driving until repair is done.
MazdaJul 18, 2017 - Use cautionVehicle
PIERCE ARROW XT (2016) recall — Equipment
Pierce is recalling 2016-2017 fire trucks with Hale Pump Interlock Modules that may fail in cold weather, preventing water pumping during emergencies. Owners must contact Pierce or Hale for free replacement.
PierceJul 18, 2017 - Lower riskMedical device
Roche Diagnostics Corporation recalls cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 +
Roche recalls cobas 6000 Modular Series systems with specific part numbers and serials to prevent operator injury during maintenance. No remedy is listed in the official notice.
RocheJul 18, 2017 - Lower riskMedical device
Becton Dickinson & Co. recalls BD MAXTM Vaginal Panel. Catalog Number(s): 443712 443710 443711 (RUO)for collection and transport of vaginal and
Becton Dickinson recalls BD MAX Vaginal Panel (catalogs 443712, 443710, 443711) due to increased unresolved and indeterminate test results, potentially requiring repeat testing.
Becton DickinsonJul 18, 2017 - Use cautionMedical device
Vyaire Medical recalls AirLife(TM) Reduced Heparin ARTERIAL BLOOD SAMPLER, REF 9025RHTR, 1ML SYRINE 25G 5/8", LUER SLIP PROTECTIVE SHEATH, 3.2
Vyaire Medical recalls AirLife Reduced Heparin arterial blood samplers (lot #0001047501) due to incorrect needle and syringe size that could cause injury during blood draws.
Vyaire MedicalJul 18, 2017 - Lower riskMedical device
Medline Industries Inc recalls Sterile Elastic Esmark Bandage, 3" x 9", individually packaged in a Tyvek plastic form fill seal pouch and placed into
Medline recalls sterile elastic bandages that may not have been properly sterilized, posing a non-sterile risk. Affected items include specific model numbers and production lots.
MedlineJul 18, 2017 - Stop using nowConsumer product
Polaris Recalls RZR 570 and RZR S 570 Recreational Off-Highway Vehicles Due to Crash and Injury Hazards (Recall Alert)
Polaris recalls 2017 RZR 570 and RZR S 570 off-highway vehicles due to front brake detachment causing crash risks. Owners must stop using and contact Polaris for free repair.
PolarisJul 18, 2017 - Stop using nowConsumer product
Corbeau USA Recalls Camlock Seat Harness Belts Due to Fall and Projectile Hazards
Corbeau USA recalls 5-Point Camlock harness belts with part numbers 53001B, 53007B, 53009B from May 2016 to May 2017 due to risk of falling out of or being thrown from vehicles, causing serious injury or death.
Corbeau USAJul 18, 2017 - Stop using nowVehicle
NISSAN VERSA (2012) recall — Air Bags
Nissan is recalling 2012 Versa models with a driver air bag inflator that may rupture due to propellant degradation, risking serious injury or death. Owners must have the inflator replaced by a dealer.
NissanJul 17, 2017
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