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
34,896 found- Lower riskFood
Italian Rose Garlic Products, LLC recalls ITALIAN ROSE GARLIC SPREAD, Gluten Free, NET WT. 35 LB (16 kg), www.italian-rose.com, Riviera Beach, FL 33404
Italian Rose Garlic Spread (35 lb gluten-free) recalled due to inadequate pH monitoring during production. FDA inspection found no documentation of mixing time or pH checks per batch. Consumers should check expiration dates and contact the company for details.
Italian RoseApr 6, 2018 - Use cautionVehicle
FOREST RIVER SURVEYOR (2018) recall — Equipment
Forest River is recalling 2018 Surveyor trailers with a refrigerator overheating risk due to missing cooling fan. Owners must have a cooling fan installed to prevent fire.
Forest RiverApr 5, 2018 - Use cautionVehicle
JAYCO PRECEPT (2019) recall — Visibility
Jayco recalls 2018-2019 Precept vehicles with faulty wiper systems that may reduce visibility in heavy snow/ice, increasing crash risk. Owners must get free relay pack replacement.
JaycoApr 5, 2018 - Use cautionVehicle
ENTEGRA VISION (2019) recall — Visibility
Entegra is recalling 2019 Vision motorhomes with faulty windshield wiper systems that may fail in heavy snow or ice, reducing driver visibility and increasing crash risk. Owners must contact Entegra for free replacement of the wiper module.
EntegraApr 5, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Lactosorb RapidFlap, bone plate, Model No. 915-0020 The RapidFlap LS Cranial Fixation System is indicated for use in
Zimmer Biomet recalls Lactosorb RapidFlap bone plate model 915-0020 with excessive chamfer on threading. This may cause improper fit during cranial surgery. Affected lots listed in the recall notice.
Zimmer BiometApr 5, 2018 - Stop using nowMedical device
Abbott recalls Thoratec HeartMate 3 LVAS Implant Kit, Rx Only, Catalog # 106524US, 106524, 10652INT - LVAS KIT, HM 3 Indicated for
Abbott recalls Thoratec HeartMate 3 LVAS Implant Kits (Rx Only) with serial numbers starting MLP 000976 due to reports of outflow graft twist occlusions causing persistent low flow alarms and serious health risks including hemodynamic compromise, thrombus, and death.
ThoratecApr 5, 2018 - Use cautionMedical device
Visaris DOO recalls Visaris Vision/Auto, ddRAura OTC APS, Diagnostic X-Ray System, Version 2.2 The Vision systems are intended for use in
Visaris recalls Vision/Auto X-Ray systems (Version 2.2) due to possible tube arm suspension failure during height adjustment, risking patient injury. Affected models include VC16B-02002 and others with specific serial numbers.
VisarisApr 5, 2018 - Stop using nowDrug
Coastal Meds, LLC. recalls LIPO-B Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
Coastal Meds recalls LIPO-B 30mL injectable due to unknown particulate matter. Discard specific lots by dates listed in the recall notice.
Coastal MedsApr 5, 2018 - Lower riskFood
Cut Fruit Express, Inc. recalls Bruschetta Mix packaged under the following brands and sizes: 1. Tastebuds, Net Wt. 12 oz. (340g), UPC 38232-37403.
Cut Fruit Express recalls Bruschetta Mix products containing undeclared milk and soy. Consumers should check product labels for specific brands and UPC codes to avoid potential allergic reactions.
Cut Fruit ExpressApr 5, 2018 - Use cautionFood
Seacrest Foods International, Inc. recalls Formagere de la Brie brand, l' Explorateur, soft ripened cheese made from pasteurized milk, product comes in a 250g
Seacrest Foods recalls Formagere de la Brie l' Explorateur soft cheese due to potential Listeria monocytogenes contamination. Consumers should avoid eating affected products with lot numbers H010 or H011.
Seacrest FoodsApr 5, 2018 - Stop using nowConsumer product
Spirit Halloween Recalls Nickelodeon PAW PATROL Marshall Hat with Flashlight Due to Fire and Burn Hazards
Spirit Halloween recalls Nickelodeon PAW PATROL Marshall hats with flashlights due to fire and burn risks from overheating batteries. Affected units include specific SKUs and date codes. Consumers must stop using and dispose of the item for full refund.
Spirit HalloweenApr 5, 2018 - Stop using nowConsumer product
Mizco International Recalls Power Bank Charging Stations Due to Fire and Burn Hazards; Sold at The Container Store
Re-fuel power bank charging stations recalled due to overheating risks. Stop using immediately and get a refund from The Container Store.
Re-fuelApr 5, 2018 - Use cautionVehicle
ZERO ZERO S (2012) recall — Electrical System
Zero Motorcycles is recalling 2012 S, DS, and DSP models due to battery cell pouches wearing, which can cause electrical shorts and fire risk. Owners can repurchase or get trade assistance.
ZeroApr 4, 2018 - Use cautionVehicle
FORD EXPEDITION (2018) recall — Power Train
Ford recalls 2018 Expedition vehicles with power train issues where gear shift may indicate wrong gear or vehicle may roll if not parked. Owners should contact Ford for free inspection.
FordApr 4, 2018 - Use cautionVehicle
FORD EXPEDITION (2018) recall — Power Train
Ford recalls 2018 Expedition vehicles with 10-speed automatic transmissions that may roll away if not parked properly, risking injury or crash. Owners must have transmission inspected for roll pin.
FordApr 4, 2018 - Use cautionMedical device
Deerfield Imaging, Inc. recalls IMRIS IMRI 1.5T AND 3T S System Product Usage: The IMRIS intraoperative MRI systems are traditional MRI systems that
Deerfield Imaging recalls IMRIS 1.5T and 3T intraoperative MRI systems due to magnetic field causing IFOSS control panel malfunction. Affected units have specific serial numbers.
Deerfield ImagingApr 4, 2018 - Use cautionMedical device
Maquet Cardiopulmonary Ag recalls CARDIOHELP Gas Bottle Holder HKH 8880, Product Code/Part Number 70105.0901 Product Usage: The Cardiohelp Gas Bottle (or
Maquet recalls Cardiohelp Gas Bottle Holder HKH 8880 due to potential clamp cracking from strong vibrations during ambulance transport. Affected units include specific product codes sold in the US and abroad.
MaquetApr 4, 2018 - Lower riskMedical device
Handpiece Headquarters recalls Henry Schein CU 1000 Halogen Curing Light, Catalog 900-4542. - Product Usage: Curing light for use in dentistry. The
Henry Schein recalls CU 1000 Halogen Curing Lights (serial #17C0001-17C0252) due to potential heat sensation during dental procedures. This recall addresses a labeling issue that may cause patient discomfort.
Handpiece HeadquartersApr 4, 2018 - Lower riskMedical device
Menarini Silicon Biosystems recalls CELLSEARCH¿ CIRCULATING Tumor Cell Kits (IVD) (Product Code 7900001) CELLSEARCH¿ CIRCULATING Tumor Cell Kit is intended
Menarini Silicon Biosystems recalls CELLSEARCH Circulating Tumor Cell Kits (Product Code 7900001) due to potential delays in reporting results from high image counts. Affected kits may require extra time for review.
Menarini Silicon BiosystemsApr 4, 2018 - Lower riskFood
Global Commodities Corp. recalls Buenas Grated coconut - frozen; Kinayod na Niyog Noix de Coco Rape; UPC: 4806514650443 Keep Frozen Net Wt. 16 oz.,
Global Commodities Corp. recalls 16oz frozen grated coconut (UPC 4806514650443) due to Salmonella contamination found in one lot. Consumers should check product details and contact the company for guidance.
Global Commodities Corp.Apr 4, 2018 - Lower riskFood
Avalanche Distributing, LLC recalls Scotcharoo Valanga Gourmet, is a crispy rice cereal with peanut butter base, with semisweet chocolate and butterscotch
Avalanche Distributing recalls Scotcharoo Valanga Gourmet cereal due to missing milk and soy declarations on labels. The product contains whey, milk, and soy lecithin but does not list these allergens.
ScotcharooApr 4, 2018 - Stop using nowConsumer product
Vornado Air Recalls Electric Space Heaters Due to Fire and Burn Hazards
Vornado VH101 Personal Vortex electric space heaters recalled due to fire and burn risks. Stop using immediately and get a refund or replacement.
VornadoApr 4, 2018 - Lower riskMeat & poultry
Good Foods Group, LLC Recalls Ready-To-Eat Chicken Products Due to Misbranding and Undeclared Allergen
USDA recalls 130 lbs of ready-to-eat curry chicken salad products for misbranding and undeclared cashews allergen. Consumers urged not to consume.
Good FoodsApr 3, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar, Model Number CP260600 Product Usage: The
Zimmer Biomet recalls Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar Model CP260600 due to potential dry blast irregularity in locking collar screws.
Zimmer BiometApr 3, 2018 - Use cautionMedical device
Baxter Healthcare Corporation recalls Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version 6) 35700BAXR Product Usage: The Baxter Sigma
Baxter recalls Sigma Spectrum Infusion Pumps with Master Drug Library (Version 6) 35700BAXR due to missing air-in-line and occlusion detection tests, which could cause serious health issues.
BaxterApr 3, 2018 - Lower riskMedical device
Roche Diagnostics Corporation recalls cobas e 801 immunoassay analyzer, cobas 8000 Modular Series The device is a fully automated, software controlled
Roche recalls cobas e 801 and cobas 8000 Modular Series analyzers due to potential plunger cracking causing impaired syringe function. Affected units have specific serial numbers.
RocheApr 3, 2018 - UnratedDrug
Kroger Specialty Pharmacy, Inc. recalls Sutent 50 mg capsules x28 NDC 00069-0550-38 42 days supply
Kroger Specialty Pharmacy recalls Sutent 50mg capsules (NDC 00069-0550-38) with 42-day supply due to lack of processing controls. Affected units dispensed between Dec 2017 and Feb 2018.
Kroger Specialty PharmacyApr 3, 2018 - Stop using nowConsumer product
Scotch Thermal Laminators Recalled by 3M Due to Burn Hazard
Scotch thermal laminators with model TL901C and teal accents are recalled due to burn hazard from overheating plastic enclosure. Consumers must stop using and get refund from 3M.
ScotchApr 3, 2018 - Lower riskMedical device
Bio-Rad Laboratories Inc recalls PR4100 Microplate Reader US, Catalog Number 45591587 Product Usage: The PR4100 Microplate Reader is a 96 well
Bio-Rad recalls PR4100 Microplate Readers with specific serial numbers due to power supply connector incompatibility that could cause system damage if incorrectly connected.
Bio-RadApr 2, 2018 - Use cautionMedical device
GE Medical Systems Ultrasound & Primary Care Diagnostics, LL recalls T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended
GE Medical Systems recalls T2100 Microflex Drive Treadmills (model numbers 2026182-002 or 2026182-004) with specific serial numbers due to a performance issue with spare parts that could cause uncontrolled walking belt motion during stress exercise tests.
GE Medical SystemsApr 2, 2018
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