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
35,025 found- Stop using nowConsumer product
Harbor Freight Tools Recalls One Stop Gardens 15,000 and 30,000 BTU Tank Top Propane Heaters Due to Burn Hazard
Harbor Freight Tools recalls 15,000 and 30,000 BTU Tank Top Propane Heaters due to wind risk melting safety shut-off feature, causing potential burn injuries if the heater tips over.
Harbor Freight ToolsJul 21, 2021 - Stop using nowConsumer product
American Outdoor Brands Recalls Caldwell Earmuffs with Rechargeable Lithium-Battery Packs Due to Fire and Burn Hazards
American Outdoor Brands recalls Caldwell Earmuffs with rechargeable lithium battery packs due to fire and burn hazards from overheating wiring. Consumers must remove batteries and get free replacements.
American Outdoor BrandsJul 21, 2021 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2022) recall — Parking Brake
Daimler Trucks North America recalls certain 2021-2022 Thomas Built C2 Saf-T-Liner school buses due to parking brake activation switch failure that may cause unintended vehicle movement.
Thomas BuiltJul 20, 2021 - Use cautionVehicle
KENWORTH T680 (2022) recall — Visibility
PACCAR recalls 2022 Kenworth T680, T880, and W990 trucks with potential windshield defrost failure, increasing crash risk. Owners must have HVAC control head replaced by dealers.
KenworthJul 20, 2021 - Use cautionVehicle
TIFFIN ALLEGRO (2021) recall — Fuel System, Diesel
Tiffin recalls 2021-2022 Allegro Bus motorhomes with Cummins L9 diesel engines due to potential fuel leaks that could cause fire if near ignition sources. Owners must have fuel hoses replaced free by dealers.
TiffinJul 20, 2021 - Use cautionVehicle
NEWMAR VENTANA (2021) recall — Steering
Newmar is recalling 2021 Ventana motorhomes due to loose tie rod clamps that could cause steering loss and crash risk. Owners must contact dealers for free tie rod clamp replacement.
NewmarJul 20, 2021 - Lower riskMedical device
BioFire Diagnostics, LLC recalls FilmArray Blood Culture Identification (BCID) Panel Product Pouch Label: FilmArray BCID Panel Part No: RFIT-ASY-0126
BioFire Diagnostics recalls FilmArray BCID Panel product pouches with part numbers RFIT-ASY-0126/0127 that may cause false negative blood culture results due to manufacturing errors.
BioFire DiagnosticsJul 20, 2021 - Use cautionMedical device
Welch Allyn Inc recalls Braun ThermoScan PRO 6000 Ear Thermometer-indicated for the intermittent measurement of human body temperature for
Welch Allyn recalls Braun ThermoScan PRO 6000 ear thermometers that may overheat if exposed to fluids and not dried properly, risking burns. Affected units have specific model and serial number formats.
Welch Al:lynJul 20, 2021 - Use cautionMedical device
Ethicon Endo-Surgery Inc recalls HARMONICHD 1000i Shears (36cm Shaft Length)-indicated for soft tissue incisions when bleeding control and minimal
Ethicon recalls HARMONICHD 1000i Shears (36cm shaft) due to potential internal component cracking causing continuous activation and burns. Affected units have specific product codes and lot numbers.
EthiconJul 20, 2021 - Use cautionMedical device
Belmont Instrument Corporation recalls CritiCool, thermoregulation device
Belmont Instrument Corporation recalls CritiCool thermoregulation devices with serial numbers starting with 99... due to premature pump failure causing HALT 4 error and potential delayed therapy. One death reported.
Belmont InstrumentJul 20, 2021 - Use cautionMedical device
NIHON KOHDEN ORANGEMED, INC recalls Nihon Kohden NKV-550 Ventilator, REF: NKV-550-U, CE 0344, UDI: (01) 00843685100012 The Nihon Kohden NKV-550 Series
Nihon Kohden recalls NKV-550 ventilators with specific serial numbers due to potential gas inlet pressure regulator defects that could cause alarms to fail or gas release noises.
Nihon KohdenJul 20, 2021 - Lower riskMedical device
Angiodynamics, Inc. recalls Solero Generator US PG, Item No. H78712740000US0, Catalog No. 12740000US
Angiodynamics recalls Solero MTA Generator units with specific serial numbers requiring software update to prevent Error 0001 during startup. Affected units must be serviced by authorized technicians.
AngiodynamicsJul 20, 2021 - UnratedDrug
HIS ENTERPRISE INC recalls Miss Slim, capsules, packaged in 10-count and 30-count box, Distributed by : His Enterprise Made in USA UPC 742137605030
His Enterprise recalls Miss Slim capsules (10-count and 30-count boxes) due to being marketed without FDA approval. Consumers should check UPC 742137605030 for affected products.
His EnterpriseJul 20, 2021 - Lower riskFood
MAGNOLIA VEGETABLE PROCESSORS recalls Wickles Relish 16oz glass jars - 6 jars per case
Magnolia Vegetable Processors recalls Wickles Relish 16oz glass jars with wrong labels. Check lot numbers for affected items.
Magnolia Vegetable ProcessorsJul 20, 2021 - Lower riskMedical device
Cordis Corporation recalls Cordis SABER PTA Balloon Dilation Catheter, 4F, REF 48004010X
Cordis recalls SABER PTA Balloon Dilation Catheter (4F, REF 48004010X) due to potential contamination in the balloon sheath that could transfer foreign material to the balloon.
CordisJul 19, 2021 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Tizanidine HCl Tablets, USP 4 mg, 150-count bottles, Rx only, Mfd By: Dr. Reddy's Laboratories limited, Srikakulam
Dr. Reddy's recalls 4mg Tizanidine tablets due to shaved tablets that may cause improper dosing. Affected lots from India, expiring 09/2023.
Dr. Reddy'sJul 19, 2021 - Lower riskDrug
Teligent Pharma, Inc. recalls Triamcinolone Acetonide Ointment USP, 0.1% 80 g cartons, Rx Only, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC
Teligent Pharma recalls 0.1% Triamcinolone Acetonide Ointment USP 80g cartons due to incorrect labeling. This Rx-only product may be mispackaged and should be checked for proper labeling.
Teligent PharmaJul 19, 2021 - Lower riskFood
Grimmway Enterprises, Inc. dba Grimmway Farms recalls Organic Baby Rainbow Carrots Brand name: O Organics 12 oz. (340 g) plastic bag UPC: 0 7989398162 8 12 oz. bag -
Grimmway Farms recalls Organic Baby Rainbow Carrots for possible Salmonella contamination. Products sold at Wegmans and GreenWise with specific UPC and lot codes are affected. Consumers should check for 9-character lot codes starting with 195, 196, or 197 ending in BF or SP.
Grimmway FarmsJul 19, 2021 - Use cautionFood
GIVE AND GO PREPARED FOODS (USA) recalls 7 Eleven Selects Chocolate Chip 3pack Mini Muffins - 2.6 oz., 16 units per tray, 6 trays per case; UPC: 0 52548-62095 0
Recall of Give and Go 3-Pack Mini Muffins (UPC 052548620950) due to potential Listeria monocytogenes contamination. Consumers should check lot codes GCC1A or GCJ1A for affected products.
Give and GoJul 17, 2021 - Stop using nowMeat & poultry
Green Dining Table, Inc. Recalls Frozen Pork Dumplings Due to Misbranding and Undeclared Allergens
Green Dining Table recalls ~183,330 lbs of frozen pork dumplings due to undeclared milk and coconut allergens. Do not consume.
HanSang / ChoripDong / PAIK'sJul 16, 2021 - Use cautionMedical device
Philips North America LLC recalls Philips, HEARTSTART, INFANT/CHILD - SMART PADS CARTRIDGE, REF: M5072A, (0-8 YEARS)< 55 lbs / 25 kg, CE 0123,
Philips recalls infant/child defibrillator pads with incorrect labeling that may delay therapy or deliver lower energy than needed for adult patients. Affected pads are for children under 8 years and less than 55 lbs.
PhilipsJul 16, 2021 - Use cautionMedical device
Teleflex Medical Europe Ltd recalls RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers: a) 170050 b) 170055 c) 170060 d)
RUSCH Slick Set Cuffed Endotracheal Tubes with specific REF and lot numbers recalled due to potential cuff inflation while pilot balloon remains flat.
RUSCHJul 16, 2021 - UnratedDrug
Alpha-Tek LLC recalls ALPHA MALE+ Male Enhancer, fruit chew strips, 1 strip per foil pouch, Distributed by Umbrella Labs, Made in the USA,
FDA recalls Alpha Male+ male enhancer chew strips due to unapproved tadalafil. Products sold in the US may contain unsafe levels of the drug without FDA approval.
Alpha-TekJul 16, 2021 - Stop using nowFood
Lipari Foods Operating Company, LLC. recalls Backcountry Dried Apricots 9ounce plastic bag 12 packages per case
Lipari Foods recalls Backcountry Dried Apricots because sulfites are not disclosed on the label, posing a risk to those with allergies.
BackcountryJul 16, 2021 - Lower riskFood
Rich Products Corp recalls f'real Made to Order Shake Base - 8 fl oz (237ml) cups Out packaging may read 'Smoothie-base' Lid may read '
Rich Products Corp recalls 8 fl oz shake base cups with undeclared milk. Products sold with 'Smoothie-base' or 'Shake-base' labels may contain milk not listed on packaging.
Rich Products CorpJul 16, 2021 - Stop using nowFood
New Dawn Nutrition, Inc. recalls Assist and Amend Advanced Digestive Enzyme Formula, Dietary Supplement, 60 capsules per bottle, Manufactured for and
New Dawn Nutrition recalls Assist and Amend Advanced Digestive Enzyme Formula due to undeclared milk, wheat, and soy. Check your bottle.
New Dawn NutritionJul 16, 2021 - Use cautionVehicle
FORD EXPLORER (2017) recall — Suspension
Ford is recalling certain 2017 Explorer vehicles due to a rear toe-link fracture risk from road salt corrosion, which can cause loss of steering control and crash. Owners must have their suspension inspected and repaired free of charge.
FordJul 15, 2021 - Use cautionVehicle
LINCOLN AVIATOR (2020) recall — Visibility
Ford is recalling 2020 Lincoln Aviators with 3.0L engines due to potential electrical wire damage causing fire. Owners must have harness inspected and repaired by dealers.
FordJul 15, 2021 - Use cautionVehicle
FORD F-350 SD (2020) recall — Power Train
Ford is recalling 2020-2021 F-350 Super Duty trucks with 6.7L diesel engines and Dana 275 axles. Deformities in the rear axle housing may cause driveshaft separation, leading to loss of power or unintended movement when in park without parking brake.
FordJul 15, 2021 - Lower riskMedical device
Cell Marque Corporation recalls Cell Marque Antibodies, PSA (ER-PR8) Mouse Monoclonal Antibody, REF: 324M-15, 324M-16
Cell Marque recalls specific antibodies due to incorrect expiry date (2023 listed vs 2022 correct). Using expired product may cause false negatives and delay diagnosis.
Cell MarqueJul 15, 2021
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