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- Use cautionConsumer product
Lifetone Technology Recalls Bedside Fire Alarm and Clocks Due to Failure to Fully Alert Consumers to a Fire
Lifetone recalls bedside fire alarms and clocks with serial numbers AC160600001-AC160604102 and AC170100001-AC170106030 due to failure to fully alert users to fires. Defective units may not properly notify hearing-impaired individuals of emergencies.
LifetoneNov 8, 2018 - Stop using nowConsumer product
H.I.S. Recalls Girl's Clothing Sets Due to Violation of Federal Lead Content Ban
Self-Esteem recalls girl's clothing sets with lead-containing necklace. Stop using and return for refund to avoid lead poisoning in children.
Self-EsteemNov 8, 2018 - Stop using nowConsumer product
American Honda Recalls Recreational Off-Highway Vehicles Due to Fire and Burn Hazards (Recall Alert)
Honda recalls 2016-2018 Pioneer 1000 side-by-side vehicles due to fire and burn risks from incorrectly installed throttle bodies. Affected vehicles require immediate stop use and repair.
HondaNov 8, 2018 - Stop using nowConsumer product
A. O. Smith Recalls Ultra-Low NOx Water Heaters Due to Fire Hazard
A. O. Smith recalls 30-50 gallon gas water heaters sold in California with serial numbers 1115-1631 due to fire risk if installed on combustible floors. Consumers must stop using and contact for repair.
A. O. SmithNov 8, 2018 - Stop using nowConsumer product
A. O. Smith Recalls 30-Gallon Gas Water Heaters Due to Fire Hazard; Sold Exclusively at Lowe's
A. O. Smith recalls 30-gallon natural gas water heaters with model G6-UT3030NV and serial numbers starting 1805-1809 due to fire hazard from potential flame arrestor failure. Consumers must stop using and contact for free repair.
A. O. SmithNov 8, 2018 - Use cautionVehicle
PIERCE ARROW XT (2016) recall — Structure
Pierce is recalling 2016 Arrow XT emergency vehicles with a bracket that may detach and fall, posing a strike risk. Owners must contact Pierce for free hardware installation by August 22, 2018.
PierceNov 7, 2018 - Use cautionVehicle
VOLKSWAGEN GOLF (2018) recall — Steering
Volkswagen recalls 2018 Golf models with steering key removal risk causing unintended rollaway. Owners must contact customer service for free switch installation.
VolkswagenNov 7, 2018 - Use cautionVehicle
KZRV SPORTSMEN (2019) recall — Equipment
KZRV recalls 2018-2019 Sportsmen trailers with propane gas leak risk at kitchen cooktop. Free inspection and repair by dealers to prevent fire.
KZRVNov 7, 2018 - UnratedMedical device
Volcano Corporation recalls Philips Volcano FFR software used in the following systems connected to the McKesson, Schwarzer, and some Philips Xper
Philips Volcano FFR software used in specific imaging systems connected to Hemodynamic Systems may cause interoperability issues. Affected units include Volcano s5i, s5ix, and CORE Mobile Imaging Systems with certain part numbers. No remedy is stated in the recall notice.
Volcano CorporationNov 7, 2018 - Lower riskMedical device
Philips Medical Systems Gmbh, DMC recalls Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System
Philips recalls CombiDiagnost R90 X-ray systems with software versions 1.0.0-1.0.2 due to potential increased radiation exposure during patient scans. Affected units may require software update or repair.
Philips Medical SystemsNov 7, 2018 - Lower riskMedical device
Hager & Meisinger Gmbh recalls Singles carbides by Meisinger, US-No: 245, Sterile R, cylinder round end; US-No 245; Reference: HMUN245-009; Shank:
Hager & Meisinger Gmbh recalls Singles carbides (US No 245) due to possible 1.0mm blade packaged in 0.9mm blade packaging. Affected items have specific model numbers and lot codes.
MeisingerNov 7, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Clopidogrel Tablets, USP, 300 mg, 30 (5 x 6 unit-dose) count blister pack, Rx only, Manufactured by Dr. Reddy's
Dr. Reddy's recalls 300 mg Clopidogrel tablets with failed dissolution testing at 18 months. This could affect medication effectiveness. Consumers should contact the manufacturer for details.
Dr. Reddy'sNov 7, 2018 - Lower riskDrug
RemedyRepack Inc. recalls Nitrofurantoin Monohydrate/Macrocrystals capsules,100 mg, packaged in HDPE 60 cc bottles, Rx only, MFG: Sandoz Inc.,
RemedyRepack recalls Nitrofurantoin 100mg capsules due to potential cross contamination with unrelated drugs like Benazepril and Haloperidol. Consumers should contact the company for details.
RemedyRepackNov 7, 2018 - Lower riskFood
Wegmans Food Markets, Inc. recalls Wegmans Placek Coffee Cake - 11 oz., UPC 77890 41407 and 22 oz., UPC 77890 39002
Wegmans recalls Placek Coffee Cake (11oz & 22oz) due to undeclared milk. Consumers should check UPCs and use by dates up to November 9, 2018.
WegmansNov 7, 2018 - Stop using nowConsumer product
Kubota Recalls Mowers and Compact Tractors Due to Burn Hazard (Recall Alert)
Kubota recalls 2014-2018 mowers and tractors with model numbers BX, GR, ZD, ZG due to risk of hot coolant spraying and causing burns. Affected units have orange and black color and specific model serial numbers.
KubotaNov 7, 2018 - Stop using nowMeat & poultry
Ganaderos Borges, Inc. Recalls Pork Products due to Possible Foreign Matter Contamination
USDA FSIS recalls 14,760 lbs of pork patties for institutional use due to possible metal contamination. Consumers are urged not to consume these products and should discard or return them.
Ganaderos BorgesNov 6, 2018 - Use cautionVehicle
FORD EDGE (2018) recall — Power Train
Ford is recalling certain 2017-2018 Edge models with 2.0L gas engines and six-speed automatic transmissions due to potential torque converter weld stud failure, which could cause vehicle loss of power and crash risk.
FordNov 6, 2018 - Use cautionMedical device
Deerfield Imaging, Inc. recalls IMRIS T2X table, Part Numbers: (a)108000-000, (b)108000-600, (c)109682-000, (d) 109682-600, (e) 110470-600 - Product
Deerfield Imaging recalls IMRIS T2X tables with specific part numbers due to potential drifting in roll position during use. Affected models may require correction to prevent patient positioning issues.
Deerfield ImagingNov 6, 2018 - Lower riskMedical device
The Binding Site Group, Ltd. recalls Binding Site Human IgM Kit (for SPAPLUS), REF: NK012.S The device consists of reaction buffer, sheep anti-IgM
The Binding Site recalls Human IgM Kit (for SPAPLUS) REF NK012.S due to calibration curve validation problems. Kit control values may report outside specified ranges.
The Binding SiteNov 6, 2018 - UnratedDrug
Breckenridge Pharmaceutical, Inc. recalls Megestrol Acetate Oral Suspension, USP 625 mg/5mL, 150 mL bottle, Rx only, Distributed by: Breckenridge Pharmaceutical,
Breckenridge Pharmaceutical recalls Megestrol Acetate Oral Suspension (625 mg/5mL) due to failed stability testing. This prescription drug may have particle size issues affecting safety.
Breckenridge PharmaceuticalNov 6, 2018 - Lower riskDrug
Takeda Development Center Americas, Inc. recalls AMITIZA (lubiprostone) capsules 8 mcg. 60-count bottle, Rx Only. Marketed by: Sucampo Pharma Americas, LLC, Rockville
Takeda recalls AMITIZA (lubiprostone) 8 mcg capsules due to elevated impurities in stability testing. This may affect safety for patients using prescription medication.
TakedaNov 6, 2018 - Stop using nowDrug
L. Perrigo Company recalls Antacid Tablets, Calcium Carbonate chewable tablets, 750mg, 60-count bottle, OTC, [Healthy Accents brand NDC:
L. Perrigo Company recalls Healthy Accents, HealthMart, and DG health calcium carbonate chewable antacid tablets due to foreign metal particles.
Healthy Accents / HealthMart / DG healthNov 6, 2018 - Lower riskFood
NEW FOREST LLC recalls Organic Cardamom Green Whole. Product of Guatemala. Product is labeled with a paper label son onto each 25-kg
New Forest LLC recalls Organic Cardamom Green Whole from Guatemala due to potential Salmonella contamination. Consumers should check labels for lot number CARDPODCD-2017-12-NF and take appropriate action if affected.
New ForestNov 6, 2018 - Lower riskFood
Ukrop's Homestyle Foods, LLC recalls Product labeled "Herb Roasted Potatoes", packed in 16oz plastic tray with clear plastic shrink-wrapping. Product is
Ukrop's Homestyle Foods recalls Herb Roasted Potatoes that were mislabeled as baked potatoes with cheddar cheese and bacon. Consumers may face allergic reactions due to undeclared allergens.
Ukrop'sNov 6, 2018 - Lower riskFood
NOW Foods recalls NOW Vitamin B-50 Complex with C 100 Veg Caps
NOW Foods recalls Vitamin B-50 Complex with C 100 Veg Caps due to mislabeling as Vitamin B-50 mg 100 Veg Caps. Product code 0420 may be mislabeled.
NOW FoodsNov 6, 2018 - Stop using nowFood
Sprout Creek Farm, Inc. recalls Margie Cheese. It is packaged with a green round label, wrapped in white milk paper in one-pound wheels.
Sprout Creek Farm recalls Margie Cheese with green round label and white milk paper packaging due to Listeria monocytogenes contamination. Consumers should check lot numbers for affected products.
Sprout Creek FarmNov 6, 2018 - Use cautionVehicle
NEWMAR MOUNTAIN AIRE (2018) recall — Tires
Newmar recalls 2016-2018 Mountain Aire motorhomes with a DEF bracket that may damage tires, increasing crash risk. Owners must have bracket moved away from tires.
NewmarNov 5, 2018 - Use cautionVehicle
INTERNATIONAL LT (2019) recall — Service Brakes, Air
Navistar recalls 2019 International LT trucks with specific feature codes for brake drum overheating that could cause separation or brake failure.
NavistarNov 5, 2018 - Lower riskMedical device
Bausch & Lomb Surgical, Inc. recalls enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated for primary implantation for the visual
Bausch & Lomb recalls enVista One Piece Hydrophobic Acrylic Intraocular lenses with cosmetic imperfections on the surface. Affected models include MX60E and specific SKUs from MXUE0000 to MXUE3400.
Bausch & LombNov 5, 2018 - Use cautionMedical device
Fresenius Medical Care Renal Therapies Group, LLC recalls Optiflux F160NR Capillary High Flux Dialyzer Single Use Only, Product Code 0500316E
Fresenius Medical Care recalls Optiflux F160NR dialyzers with specific lot numbers due to potential external blood leaks. Affected units may require replacement.
Fresenius Medical CareNov 5, 2018
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