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- Lower riskDrug
Ultra Seal Corporation recalls Advance Formula Pain Reliever (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 tablets Per Packet,
Ultra Seal Corporation recalls Advance Formula Pain Reliever tablets due to unstable salicylic acid levels. Affected lots have specific expiration dates and packaging details. Consumers should check their product labels for the lot numbers and expiration dates listed.
Ultra Seal CorporationOct 13, 2021 - Lower riskFood
The Kroger Co recalls Country Oven Yellow/Caramel Cake Single Slices, double layer cakes ( 48oz )
Kroger recalls Country Oven Yellow/Caramel Cake Single Slices (48oz) due to possible metal fragments in starch. Consumers should check UPCs and use by dates for affected products.
KrogerOct 13, 2021 - Stop using nowConsumer product
Specialized Bicycle Components Recalls Tarmac SL7 Bicycles and Framesets Due to Fall and Injury Hazards
Specialized recalls Tarmac SL7 bicycles and framesets due to fork steerer tube cracks from potholes, risking falls and injuries. Consumers must stop using and get free repairs.
SpecializedOct 13, 2021 - Lower riskMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Medtronic CareLink SmartSync Device Manager application software (D00U005) used by the following Medtronic Cobalt and
Medtronic recalls CareLink SmartSync Device Manager software (D00U005) for Cobalt and Crome ICDs/CRT-Ds due to potential data processing failures. Affected units may not correctly track heart health episodes.
MedtronicOct 12, 2021 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis pheno with software VE20C- diagnostic imaging angiography system Model: 10849000
Siemens recalls Artis pheno diagnostic imaging angiography systems with software VE20C (model 10849000) due to four software issues that may cause image corruption, system shutdowns, or inability to perform X-rays during procedures.
SiemensOct 12, 2021 - Lower riskMedical device
Medtronic Perfusion Systems recalls Medtronic Custom Perfusion kits, with the following product descriptions and corresponding model numbers: 1. CUSTOM
Medtronic recalls 48 specific perfusion kit models due to endotoxin testing not being conducted, which may pose a risk of infection in medical use.
Medtronic Perfusion SystemsOct 12, 2021 - Lower riskDrug
Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals recalls Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count
BRP Pharmaceuticals recalls methocarbamol tablets labeled as 500mg but containing 750mg due to labeling error. Consumers should check product details and contact the company for guidance.
BRP PharmaceuticalsOct 12, 2021 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls AllerClear D-24 hr, (Loratadine and Pseudoephedrine Sulfate, Extended-Release Tablets, USP 10/240mg), 15-count blister
Sun Pharmaceutical recalls AllerClear D-24 hr tablets due to failed moisture limits. This may cause reduced effectiveness or safety issues. Check your product for the NDC 63981-724-15 label.
Sun Pharmaceutical IndustriesOct 12, 2021 - UnratedDrug
Lupin Pharmaceuticals Inc. recalls Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 count (NDC 68180-414-06) and b) 90 count (NDC
Lupin Pharmaceuticals recalls specific lots of Irbesartan and Hydrochlorothiazide tablets due to detected impurity N-nitrosoirbesartan in the manufacturing process.
LupinOct 12, 2021 - UnratedDrug
Teligent Pharma, Inc. recalls Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL), 50 mL glass bottles, Rx Only, Teligent Pharma Inc., Buena,
Teligent Pharma recalls 50mL glass Lidocaine 4% topical solution (Rx only) due to superpotent drug hazard. Product sold with specific lot numbers and expiration dates.
Teligent PharmaOct 12, 2021 - Lower riskDrug
Vita Pharmacy, LLC dba Talon Compounding Pharmacy recalls B COMPLEX INJ CMP-NO B12, NO LIDOCAINE INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste
Talon Compounding Pharmacy recalls B Complex injectables (no lidocaine) due to lack of sterility assurance. This may cause infections if used. Check lot numbers for affected products.
Talon Compounding PharmacyOct 12, 2021 - Lower riskFood
The Mustard Man Inc recalls The Mustard Man Inc Simply Peppered Mustard 8oz plastic bottles, 6 bottles per case
The Mustard Man Inc recalls 8oz Simply Peppered Mustard bottles that were filled with Simply Horsey Mustard. Consumers should check batch numbers and return affected products.
The Mustard Man IncOct 12, 2021 - Use cautionVehicle
MASERATI QUATTROPORTE (2021) recall — Fuel System, Gasoline
Maserati is recalling 2021 Quattroporte vehicles with a potential fuel leak that could cause engine stalls or fire. Owners must have the fuel line sensor housing replaced free of charge by dealers.
MaseratiOct 11, 2021 - Use cautionVehicle
JEEP GRAND CHEROKEE (2021) recall — Air Bags
Chrysler recalls 2021 Jeep Grand Cherokee models with potential air bag disablement due to software issues. Owners must contact dealers for free reprogramming to prevent injury risks in crashes.
ChryslerOct 11, 2021 - Use cautionVehicle
FORD EXPLORER (2021) recall — Suspension
Ford is recalling certain 2021 Explorer vehicles with incorrect rear suspension components that may affect handling and increase crash risk. Owners must have their suspension inspected and repaired free by dealers.
FordOct 11, 2021 - Use cautionVehicle
FORD ESCAPE (2021) recall — Electrical System
Ford is recalling one 2021 Escape with a 2.5L hybrid powertrain due to potential sudden loss of drive power causing crash risk. Free battery replacement available.
FordOct 11, 2021 - Use cautionVehicle
AUDI A4 (2020) recall — Seats
Audi is recalling certain 2017-2020 A4 models due to a faulty seat heater cable that can disable the passenger airbag during crashes. Owners must have the seat repaired free of charge.
AudiOct 11, 2021 - Lower riskMedical device
BioFire Diagnostics, LLC recalls BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog
BioFire recalls BCID2 blood culture panels with possible false Acinetobacter calcoaceticus-baumannii complex results due to non-viable contamination in vials. Affected panels expire by April 30, 2022.
BioFireOct 11, 2021 - Use cautionMedical device
Forbes Rehab Services Inc recalls Affected components are limited to the Monoprice charging cable (Product # 4867) and 24W iClever Boost Cube charging
Forbes Rehab Services recalls Monoprice charging cables and iClever Boost Cube chargers that may cause fire or electric shock if damaged or used with moisture. Affected units include specific SoundPOD Bluetooth Speaker accessories for ProSlate speech devices.
Forbes Rehab ServicesOct 11, 2021 - Lower riskMedical device
Jjgc Industria E Comercio De Materials Dentarios Sa recalls GM Helix Acqua Implant 3.5x10, Article No. 140.944
GM Helix Ac: 3.5x10 implants mislabeled as 3.5x10mm. Low bone quality may cause nerve damage if incorrect size installed. Affected units: UDI 7899878024897, Lots GNW15 and GRE82.
Jjgc IndustriaOct 11, 2021 - Lower riskMedical device
Clark Laboratories, Inc. recalls Bartels Legionella Urinary Antigen- an adjunct to culture for the presumptive diagnosis of past or current
Clark Laboratories recalls Bartels Legionella Urinary Antigen test kits due to potential pipetting issues causing invalid results. Affected units include specific product codes and lots.
Clark LaboratoriesOct 11, 2021 - Use cautionVehicle
NISSAN PATHFINDER (2022) recall — Latches/Locks/Linkages
Nissan recalls 2022 Pathfinder vehicles with potential hood latch detachment causing obstructed driver view and crash risk. Owners must have secondary hood latch bracket inspected and replaced by dealers.
NissanOct 9, 2021 - Use cautionVehicle
GMC ACADIA (2022) recall — Air Bags
General Motors recalls 2022 GMC Acadia vehicles with air bags that won't deploy in crashes due to unactivated SDM. Owners must return vehicles to assembly plant for activation.
GMCOct 9, 2021 - Use cautionVehicle
MASERATI QUATTROPORTE (2021) recall — Seat Belts
Maserati recalls 2021 Quattroporte vehicles with seat belt issues that may cause child restraints to fail during crashes. Owners must have seat belts inspected and replaced by dealers.
MaseratiOct 9, 2021 - Stop using nowMeat & poultry
Nick’s Famous Bar-B-Q Recalls Ready-To-Eat Pork Products Due to Possible Listeria Contamination
USDA recalls 3,140 pounds of ready-to-eat smoked pork from Nick's Famous Bar-B-Q due to possible Listeria monocytogenes contamination. Products may cause serious infections in high-risk groups like pregnant women and older adults.
Nick's Famous Bar-B-QOct 8, 2021 - Stop using nowMeat & poultry
Crider Foods Recalls Canned Beef With Gravy Products Due to Possible Unsafe Levels of Lead From Outside Source
Crider Foods recalls 684,774 pounds of canned beef with gravy products due to possible lead contamination from an outside spice supplier. Consumers are urged not to consume these products.
Crider FoodsOct 8, 2021 - Use cautionVehicle
FORD ESCAPE (2021) recall — Fuel System, Gasoline
Ford is recalling 2021 Escape vehicles with a fuel delivery module that may leak, causing engine stalls and crash risk. Owners must have the module replaced free by dealers.
FordOct 8, 2021 - Use cautionVehicle
POLARIS SLINGSHOT (2020) recall — Wheels
Polaris recalls 2020-2021 Slingshot vehicles with loose rear wheel studs that could detach, causing crashes. Owners must have dealers inspect and replace parts free.
PolarisOct 8, 2021 - Use cautionVehicle
HUSQVARNA VITPILEN 701 (2020) recall — Structure
KTM recalls 2020 Husqvarna 701 Vitpilen motorcycles due to license plate bracket interference with rear wheel, potentially causing crashes. Owners must get free inspection and realignment by dealers.
KTMOct 8, 2021 - Lower riskMedical device
Beaver Visitec International, Inc. recalls bvi CustomEyes Kit-Lafayette General Medical Center: CustomEyes Cataract Surgical Kits that contain Beaver Xstar
Beaver Visitec recalls CustomEyes cataract surgical kits containing bevel-up blades instead of bevel-down. Affected kits have specific model numbers and lot numbers.
Beaver Visite: CustomEyesOct 8, 2021
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83,613 recalls tracked · 72,041 explained in plain English · 10,977 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.