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
34,956 found- Lower riskMedical device
Siemens Healthcare Diagnostics, Inc recalls SiemensADVIA Centaur aTG (500 test kit) Siemens Material Number (SMN): 10492399
Siemens recalls ADVIA Centaur aTG (500 test kit) lots ending in 316 or lower due to positive bias against WHO reference standards. Affected kits may give inaccurate thyroid hormone results.
SiemensDec 7, 2018 - Lower riskDrug
Sun Pharmaceutical Industries, Inc. recalls Absorica (Isotretinoin) Capsules 30 mg USP, 30 capsules (3x10 Prescription Packs) Rx only, Manufactured by: Galephar
Sun Pharmaceutical recalls Absorica 30mg capsules due to lower-than-stated isotretinoin content. Affected lots may pose reduced effectiveness risks. Contact for return instructions.
Sun PharmaceuticalDec 7, 2018 - Lower riskDrug
US Pharmaceuticals Inc. recalls Soothe & Cool Protect Moisture Guard Skin Protectant (petrolatum 59%),3.5 oz tubes, Manufactured in USA for: Medline
US Pharmaceuticals recalls 3.5 oz Soothe & Cool Protect Moisture Guard tubes due to microbial contamination in purified water. Affected products have specific lot numbers and expiration dates.
US PharmaceuticalsDec 7, 2018 - Stop using nowFood
Procesadora de Dulces Tipicos, S.A. de C.V. recalls Tamy Pop 18 pieces Net Wt. 1 lb. 15.7 oz. packaged in a clear plastic jar, 6 jars per case
Procesadora de Dulces Tipicos recalls Tamy Pop candy jars due to undeclared soy. Check lot numbers and UPC for details.
Tamy PopDec 7, 2018 - Lower riskFood
Threshold Enterprises Ltd recalls Planetary Herbals Mullein Lung Complex; 1000 mg; 15 count, item number PF0003; 90 count - Item number PF0002; 180
Planetary Herbals is recalling Mullein Lung Complex products due to a labeling error indicating incorrect inactive ingredients. Consumers should check product numbers and lot dates for affected items.
Planetary HerbalsDec 7, 2018 - Lower riskFood
Moonstruck Chocolate Company recalls The Salty Nutty Toffee Bar, brand ALMA, net weight 1.85 oz. UPC on individual bar: 8 58533 00602 8 UPC on master case 0
Moonstruck Chocolate Company recalls ALMA Salty Nutty Toffee Bars (1.85 oz) due to undeclared soy lecithin. Consumers should check UPCs for affected items.
ALMADec 7, 2018 - Use cautionVehicle
LAMBORGHINI AVENTADOR (2014) recall — Engine And Engine Cooling
Lamborghini recalls 2012-2018 Aventador models due to potential engine stall causing crashes. Owners must contact customer service for free software update by August 3, 2018.
LamborghiniDec 6, 2018 - Use cautionVehicle
NEW FLYER XD60 (2017) recall — Service Brakes, Air
New Flyer recalls 2017 XD60 buses with potential brake failure due to guide pin breakage. Owners must contact for free brake repair by June 29, 2018.
New FlyerDec 6, 2018 - Use cautionVehicle
KME PREDATOR AERIAL (2018) recall — Equipment
KME is recalling 2015-2018 Predator Aerials with tether control issues that could cause injury if unplugged during operation. Get free software update to fix.
KMEDec 6, 2018 - Use cautionVehicle
FORD EXPEDITION (2018) recall — Fuel System, Gasoline
Ford is recalling 2018 Expedition models with potential fuel leaks that could cause fire if near ignition sources. Owners must have the high-pressure fuel pump replaced free of charge by dealers.
FordDec 6, 2018 - Lower riskMedical device
Hologic, Inc. recalls I-View¿ Contrast Enhanced Digital Mammography, ASY-08109
Hologic recalls I-View Contrast Enhanced Digital Mammography units due to calibration issues affecting contrast visualization in subtracted images. All units are affected.
HologicDec 6, 2018 - Lower riskMedical device
Bard Medical Division recalls BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature Sensing Infection Control Foley Catheter with
Bard Medical Division recalls SureStep Foley Tray Systems with catalog number A319418AM and lot NGCT1929 due to potential urine leaks from vented sample ports. Affected units may require replacement to prevent infection.
Bard Medical DivisionDec 6, 2018 - Lower riskMedical device
Medtronic Navigation, Inc. recalls Medtronic Adapter Percutaneous Pin, REF 9734752 (GTIN 00643169529489) and REF 9734752-G02 (GTIN 00763000054915),
Medtronic recalls specific percutaneous pin adapters used in StealthAir Frame Assembly. The adapter may rotate slightly after surgical placement and not return to original position, potentially causing complications.
MedtronicDec 6, 2018 - Use cautionMedical device
Carl Zeiss Meditec, Inc. recalls VisuMax Software Version 2.10.13 with activated Software-Module ReLEx (SMILE) option used in conjunction with the
Carl Zeiss Meditec recalls VisuMax software version 2.10.13 with activated ReLEx (SMILE) option due to potential incorrect corneal cuts during eye surgery. Affected devices may perform cap cuts instead of flap cuts, risking vision complications.
Carl Zeiss MeditecDec 6, 2018 - Lower riskMedical device
Vygon U.S.A. recalls Vygon DUALSTOP Red Cap used for intravascular lines Product Code: 9888.00 - Product Usage: Cap used for intravascular
Vygon recalls DUALSTOP Red Caps for intravascular lines due to leaks. Product code 9888.00 with specific lot codes. Affected users should check their caps and contact Vygon for details.
VygonDec 6, 2018 - Use cautionDrug
Pfizer Inc. recalls Levoxyl (levothyroxine sodium tablets, USP) tablets 112 mcg, 100-count bottle, Rx Only,Distributed by Pfizer Inc. New
Pfizer recalls 112 mcg Levoxyl tablets due to superpotent drug risk. This may cause serious health issues if taken without medical supervision.
PfizerDec 6, 2018 - Stop using nowFood
Mariner Seafood, LLC recalls Salmon packaged in a plastic container; HELLO QUALITY PACIFIC SILVERSIDE SALMON Hello FRESH NET WT. 10oz (283g) with
Mariner Seafood recalls 10oz frozen salmon products due to Listeria monocytogenes contamination. Consumers should avoid these items as they pose a risk of serious illness.
Mariner SeafoodDec 6, 2018 - Stop using nowConsumer product
Skip Hop Recalls Convertible High Chairs Due to Injury and Fall Hazards
Skip Hop recalls Tuo convertible high chairs with detachable legs that pose fall and injury risks to children. Consumers must stop using and get a refund or $200 gift card.
Skip HopDec 6, 2018 - Stop using nowConsumer product
Meijer Recalls Children's Hooded Jackets Due to Choking Hazard
Meijer recalls Falls Creek Kids children's hoodies due to risk of zipper slider detaching and causing choking in young children. Consumers should stop using and return for full refund.
Falls Creek KidsDec 6, 2018 - Stop using nowConsumer product
Kawasaki USA Recalls Off-Highway Utility Vehicles Due to Injury Hazard (Recall Alert)
Kawasaki recalls 2018-2019 Mule Pro utility vehicles due to potential rollover protection failure, risking injury. Owners must stop use and contact a dealer for free repair.
KawasakiDec 6, 2018 - Lower riskMedical device
Beckman Coulter Inc. recalls UniCel DxC 660i, 680i, 860i, and 880i SYNCHRON Access Clinical Systems, that are re-configured so that the DxI system
Beckman Coulter recalls UniCel DxC 660i, 680i, 860i, and 880i systems with software reconfiguration that may cause incorrect lab results due to sample mishandling during aliquot creation.
Beckman CoulterDec 5, 2018 - Lower riskMedical device
Medela Inc recalls Breast Milk Transfer Lid for use with Oral Syringe Connectors Model: 90003S-100
Medela recalls breast milk transfer lids (model 90003S-100) due to potential packaging breaches that could compromise sterility. Affected units have specific lot codes.
MedelaDec 5, 2018 - Lower riskMedical device
Sage Products Inc recalls Toothete Oral Care Sodium Bicarbonate Mouthpaste, Net Wt. 1/3 oz/ 9g, included in Independent Care System. The system
Sage Products Inc recalls lot 67924 of Independent Care System oral care kits due to potential damage to Sodium Bicarbonate Mouthpaste tubes.
Independent Care SystemDec 5, 2018 - Lower riskMedical device
Exactech, Inc. recalls Equinoxe Preserve Humeral Stem, 8mm Product Usage: The Equinoxe Preserve Stems are indicated for use in skeletally
Exactech recalls Equinoxe Preserve Humeral Stem 8mm implants due to potential inclusion of Optetrak Knee System instructions instead of correct usage guide. Affected units have specific serial numbers and catalog codes.
ExactechDec 5, 2018 - Lower riskDrug
Pharmedium Services, LLC recalls Fentanyl Citrate 2 mcg per mL (200 mcg per 100 mL) and Ropivacaine HCl 0.2% in Sodium Chloride 0.9%, Injection, 100 mL
PharMEDium Services recalls specific fentanyl and ropivacaine injections due to sub-potent risk. Learn product details and safety steps.
PharMEDiumDec 5, 2018 - Lower riskFood
Dr Jackson recalls DR. JACKSON'S RELAX TEA (ANTI-ANXIETY) 500mL Net Wt 49g; UPC Code: 5 060309 140239. Tea bags are packaged in a glass
Dr Jackson recalls Relax Tea (anti-anxiety) due to potential mold contamination. Affected products include 500mL net weight 49g with UPC 5 06030:140239. No remedy specified in recall notice.
Dr JacksonDec 5, 2018 - Lower riskFood
DANONE WATERS OF AMERICA INC recalls LIGHT & FIT¿ GREEK CRUNCH NONFAT YOGURT & TOPPINGS S MORES FLAVOR, 5 oz Preformed cups with a topper, Refrigeration
Danone recalls Light & Fit Greek Crunch Nonfat Yogurt with peanuts in toppers due to improper labeling. Consumers should check UPC 36632 03825 for affected products.
DanoneDec 5, 2018 - Stop using nowMeat & poultry
JBS Tolleson, Inc. Recalls Raw Beef Products due to Possible Salmonella Newport Contamination
JBS Tolleson recalls over 12 million lbs of raw beef for possible Salmonella Newport contamination. Discard or return products immediately.
JBS TollesonDec 4, 2018 - Use cautionVehicle
JEEP WRANGLER (2018) recall — Structure
Chrysler recalls 2018 Jeep Wrangler vehicles where rear floor pan corrosion may cause seat detachment during crashes. Owners must have their rear underbody ladder rail inspected for rust protection.
ChryslerDec 4, 2018 - Use cautionVehicle
FOREST RIVER SALEM (2018) recall — Equipment
Forest River is recalling 2018 Salem trailers with incorrect tire pressure placards that could lead to crashes. Owners must check for 54 PSI placards and update to 65 PSI.
Forest RiverDec 4, 2018
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