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
VIRTUS PHARMACEUTICALS LLC. recalls Virt-Nate Tablets, Number of units per package: 100 Tablets Package Type: 100 Tablets/Bottle
Virtus Pharmaceuticals is recalling Virt-Nate Tablets because product labels do not show the correct Dietary Folate Equivalents (DFEs) as calculated by the product formulation. This could lead to inaccurate folate intake.
Virtus PharmaceuticalsAug 3, 2018 - Lower riskFood
Zakah Life LLC recalls Super Green Maeng Da Premium Kratom, Zakah Life Dietary Supplement, Mitragyn Speciosa, packaged in 1) 90 capsules, 500
Zakah Life recalls Super Green Maeng Da Premium Kratom due to potential Salmonella contamination in red and green strains. The product may cause illness if consumed. Consumers should check labels for 90-capsule or 100g bags.
Zakah LifeAug 3, 2018 - Lower riskFood
The Coca-Cola Company recalls Consumer Packaging (PET bottle): Minute Maid TROPICAL BLEND Flavored Juice Beverage 12 FL OZ (355mL), JAN0719NPA, UPC:
Coca-Cola recalls Minute Maid Tropical Blend 12 fl oz juice bottles from July 2018 due to glass found in samples. Consumers should check product codes and contact customer service for details.
Coca-ColaAug 3, 2018 - Lower riskFood
J R Simplot Co Corporate HQ recalls Simplot Good Grains Exotic Grains & Fire-Roasted Vegetable Blend, Net Wt. 15 lbs (6 / 2.5 lb bags per case), UPC
Simplot recalls 15-lb exotic grains blend due to undeclared wheat. This gluten-free product may contain wheat, posing a risk for those with celiac disease or gluten allergies.
SimplotAug 3, 2018 - Lower riskFood
Market of Choice Inc recalls Mediterranean Salad Vegan, pre-packaged. UPC 0 211004 706991.
Market of Choice Inc recalls Mediterranean Salad Vegan pre-packaged items due to milk not being declared in the Contains statement. This may affect product labeling compliance.
Market of ChoiceAug 3, 2018 - Use cautionVehicle
DODGE CARAVAN (2017) recall — Exterior Lighting
Chrysler recalls 2017 Dodge Caravan vehicles with faulty brake switches that may keep brake lights on or allow shifting out of park without braking. Owners should contact Chrysler for free replacement.
ChryslerAug 2, 2018 - Use cautionVehicle
RAM 1500 (2018) recall — Power Train
Chrysler recalls 2017-2018 RAM 1500 models with column shift for unintended rollaway risk if transmission shifts out of park without brake pedal or key.
ChryslerAug 2, 2018 - Lower riskMedical device
Acumedia Manufacturers, Inc. recalls Campylobacter Blood Free Selective Medium, PN 7527A Used with cefoperazone for the selective isolation of Campylobacter
Acumedia recalls Campylobacter Blood Free Selective Medium (PN 7527A) due to incorrect expiration date labeling. This lab product may expire prematurely, but does not pose immediate health risks.
AcumediaAug 2, 2018 - Lower riskMedical device
Acumedia Manufacturers, Inc. recalls Palcam Agar Base, Acumedia, PN 7669, Product Usage - Dehydrated culture media used with supplements as a selective and
Acumedia recalls Palcam Agar Base (PN 7669) due to incorrect expiration date on label. The label shows November 30, 2021 instead of the correct November 30, 2020. This may affect lab use of the product.
AcumediaAug 2, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment, Model Number 185224 Intended for use in Total
Zimmer Biomet recalls Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment (Model 185224) due to one bolt missing from sterile package. This could cause improper implant fixation.
Zimmer BiometAug 2, 2018 - Lower riskMedical device
Ventana Medical Systems Inc recalls INFORM HPV III Fam 16 Probe - US Export, Catalog Number 05278856001, model 800-4295 Immunohistochemistry (IHC) for in
Ventana recalls HPV III Fam 16 Probe (model 800-4295) due to risk of false negative immunohistochemistry results from leaking reagent dispensers. Affected units sold in US with specific catalog number and lot.
VentanaAug 2, 2018 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium tablets, 40 mg, 500-count bottle, Rx only, Mfd By: Dr. Reddy's Laboratories Limited, Srikakulam -
Dr. Reddy's recalls 40mg Atorvastatin Calcium tablets (500-count) due to impurity issues detected at 18 months. Consumers should check NDC 55111-123-05 for affected products.
Dr. Reddy'sAug 2, 2018 - UnratedDrug
Pharmcore Inc. recalls Ipamorelin 3 mg Lyophilized 1 vial 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009
Pharmcore recalls Ipamorelin 3mg lyophilized vials due to lack of sterility assurance. Affected lots expire July 2018. No remedy specified in official notice.
PharmcoreAug 2, 2018 - Lower riskFood
Super Store Industries-Turlock Dairy Division recalls Sunny Side Farms Peanut Butter Cup Ice Cream; 48 oz. carton, 1.5 QTS (1.42L) UPC: 7-17544-20740 5 Allergens for Peanut
Super Store Industries recalls Sunny Side Farms Peanut Butter Cup Ice Cream due to butter pecan flavor lid containing butter pecan ice cream instead of peanut butter cup. Allergen cross-contamination risk for peanuts and tree nuts.
Sunny Side FarmsAug 2, 2018 - Stop using nowConsumer product
Zebra Technologies Expands Recall of Power Supply Units for Thermal Printers Due to Fire Hazard
Recall of Zebra power supply units (manufactured 2006-2012) that can overheat and cause fire. Owners must stop using and return for free replacement.
ZebraAug 2, 2018 - Stop using nowConsumer product
Rena Ware Recalls Nutrex Pressure Cookers Due to Burn Hazard (Recall Alert)
Rena Ware recalls Nutrex pressure cookers due to burn hazards. Stop using immediately and contact Rena Ware for a free repair.
NutrexAug 2, 2018 - Stop using nowConsumer product
Miller Fireworks Recalls Fireworks Due to Violation of Federal Standard; Explosion and Burn Hazards
Miller recalls ball bullet rocket fireworks (LB6103) and M-150 crackers (LA150B) due to overloaded pyrotechnics violating federal safety standards, risking explosions and burns. Return to store for refund.
MillerAug 2, 2018 - Stop using nowConsumer product
Clean Republic Recalls Hill Topper Electric Bike Motor Controllers Due to Crash and Injury Hazards
Hill Topper recalls motor controllers that may accelerate on their own. Stop using them now and contact the company for a free replacement.
Hill TopperAug 2, 2018 - Use cautionConsumer product
Arctic Cat Snowmobiles Recalled by Textron Specialized Vehicles Due to Injury Hazard (Recall Alert)
Recalled Arctic Cat 2018-2019 Pantera snowmobiles (VIN 100529-100848) have a handgrip that can break, causing rider injury. Consumers must stop using and contact Arctic Cat for free repair.
Arctic CatAug 2, 2018 - Stop using nowVehicle
LAND ROVER RANGE ROVER (2010) recall — Air Bags
Land Rover is recalling certain 2010 Range Rovers due to potential air bag inflator explosions causing serious injury or death. Owners must have the front passenger air bag assembly replaced free of charge by dealers.
Land RoverAug 1, 2018 - Use cautionVehicle
LAND ROVER RANGE ROVER (2012) recall — Air Bags
Land Rover is recalling 2011-2012 Range Rovers for potential air bag inflator explosions that could cause serious injury or death during crashes.
Land RoverAug 1, 2018 - Stop using nowVehicle
JAGUAR XF (2013) recall — Air Bags
Jaguar is recalling certain 2013 XF vehicles due to a risk of air bag inflator explosions causing serious injury or death. Owners must have the front passenger air bag assembly replaced free of charge.
JaguarAug 1, 2018 - Stop using nowVehicle
JAGUAR XF (2015) recall — Air Bags
Jaguar is recalling 2014-2015 XF vehicles with potentially dangerous air bag inflators that could explode during deployment, causing serious injury or death. Owners must have the front passenger air bag assembly replaced free of charge.
JaguarAug 1, 2018 - UnratedMedical device
Allied Vision Group Inc recalls Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile.
Allied Vision Group recalls Alcon Air Optix Night & Day Aqua contact lenses for potential counterfeit products imported to the U.S. Check labels for lot numbers 31202568, 31255298, 31257909, 31229117, or 31252252.
Allied Vision GroupAug 1, 2018 - Use cautionMedical device
ICU Medical Inc recalls Plum 360 Infusion System With MedNet/ Smart Card Plug And Play Module, Model # 30010. Infusion pump.
ICU Medical recalls Plum 360 Infusion Systems with specific software versions when used with MedNet Custom Drug Libraries, which can become inoperable and show a blank screen.
ICU MedicalAug 1, 2018 - Lower riskMedical device
EOS Imaging recalls sterEOS workstation
EOS Imaging recalls sterEOS workstation software versions due to potential 3D projection errors affecting clinical decisions. All software versions are impacted.
EOS ImagingAug 1, 2018 - Lower riskMedical device
Instrumentation Laboratory Co. recalls Hemosll ReadiPlasTin (10 mL Size), Part Number 0020301300 - Product Usage - HemosIL¿ ReadiPlasTin is an in vitro
Instrumentation Laboratory Co. recalls HemosIL ReadiPlasTin 10mL (Part 0020301300) due to potential for inaccurate test results. This affects users of coagulation tests on ACL TOP analyzers.
HemosILAug 1, 2018 - Lower riskMedical device
Mobius Imaging, LLC recalls AIRO Mobile CT System Model # MobiCT-32
Mobius Imaging recalls AIRO Mobile CT System Model MobiCT-32 with software version 2.0.0.0 due to potential undetected scan errors. Affected units may not alert operators of a faulty tube current modulation feature after scans complete.
Mobius ImagingAug 1, 2018 - Lower riskMedical device
COVIDIEN LLC recalls Kerlix Bandage Roll, 100 Cotton, 8 Ply, Large 4-1/2 x 9.3 (11.4 cm x 2.8 m), REF 6716 Product Usage: Used as both
Covidien recalls Kerlix bandage rolls with potential sterility breach due to seal defects. Affected lots: 18E071762, 18E072262, 18E072362, 18E132262, 18E132362. Stop using if seal appears pinched.
CovidienAug 1, 2018 - Lower riskDrug
American Health Packaging recalls Doxycycline Hyclate Tablets, USP, 100 mg, 30 Tablets per carton (3 x 10 Unit Dose Blisters), Rx Only, Distributed by:
American Health Packaging recalls 100mg Doxycycline Hyclate Tablets due to failed dissolution test. These prescription-only tablets may not release medication properly. Consumers should contact the manufacturer for details.
American Health PackagingAug 1, 2018
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