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
34,893 found- Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2018) recall — Equipment
Daimler Trucks North America recalls 2005-2018 Thomas Built Buses Saf-T-Liner C2 transit buses due to potential wheelchair dislodgement in crashes. Owners must contact DTNA for free fastener reinforcement.
Thomas Built BusesJul 17, 2017 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2018) recall — Equipment
Daimler Trucks North America recalls 2005-2018 Thomas Built Buses Saf-T-Liner C2 school buses due to potential wheelchair pocket track anchorage failure during crashes, increasing injury risk.
Thomas Built BusesJul 17, 2017 - Use cautionVehicle
FREIGHTLINER M2 BUSINESS CLASS (2018) recall — Equipment
Daimler Trucks North America recalls 2018 Freightliner M2 Business Class trucks with potential tow hook failure during recovery operations. Owners must have tow hooks inspected and replaced if needed.
Daimler Trucks North AmericaJul 17, 2017 - Use cautionMedical device
RAYSEARCH LABORATORIES AB recalls RayStation Product Usage: is a software system designed for treatment planning and analysis of radiation therapy. The
RaySearch Laboratories recalls RayStation 6 software versions 6.0.0.24, 6.1.0.26, 6.1.1.2, and 6.2.0.7 due to potential incorrect radiation dose calculations during proton therapy QA checks.
RaySearch LaboratoriesJul 17, 2017 - Use cautionMedical device
Maquet Datascope Corp - Cardiac Assist Division recalls CS 100 Intra-Aortic Balloon Pump. It supports the heart's left ventricle by increasing coronary perfusion and reducing
Maquet Datascope recalls CS 100 Intra-Aortic Balloon Pumps due to false blood back detection alarms and fluid ingress that could stop heart support therapy.
Maquet DatascopeJul 17, 2017 - Use cautionMedical device
Philips Electronics North America Corporation recalls ECG Out Cable - Heartstart MRx M1783A/M5526A 12-pin Sync cables All units of Philips sync cables model M1783A and
Philips recalls Heartstart MRx ECG out cables (M1783A/M5526A) due to potential EFT interference causing misinterpreted heart signals. Affected units sold from 2002-2014.
PhilipsJul 17, 2017 - Lower riskMedical device
Covidien LP recalls Covidien Vistec" X-Ray Detectable Sponges, 7317 Vistec" X-Ray Detectable Sponges Sponge. product Usage: Vistec X-Ray
Covidien is recalling two lots of X-ray detectable sponges due to possible contamination with human blood during manufacturing. These sponges are used for internal bleeding control and may pose a risk if contaminated.
CovidienJul 17, 2017 - Stop using nowDrug
BESTHERBS COFFEE LLC recalls New Kopi Jantan Tradisional Natural Herbs Coffee, packaged in 13 gram red packets, and each box contains 25 packets,
Bestherbs Coffee LLC recalls 25-packet boxes of New Kopi Jantan Tradisional Natural Herbs Coffee due to undeclared desmethyl carbodenafil and milk. Consumers should stop using the product immediately.
Bestherbs CoffeeJul 17, 2017 - Lower riskDrug
Linde Eckstein Gmbh + Co KG recalls Beautipharm Body Moisturizing Balm SPF 10 (Octocrylene 4% and Octyl methoxycinnamide 4%) Body Lotion, 8.3 oz. Net. Wt.
Linde Eckstein Gmbh recalls Beautipharm body moisturizing balm SPF 10 due to unverified sun protection claims. Products may not provide full SPF 10 protection as labeled.
BeautipharmJul 17, 2017 - Stop using nowDrug
Vi-Jon, Inc. recalls Magnesium Citrate Oral Solution, packaged in a 10 fl. oz. (296 mL) glass bottle, OTC, labeled as: a) GoodSense
Vi-Jon recalls Magnesium Citrate Oral Solution with mold contamination. Product contains Rhinocladiella similis mold. Consumers should stop using affected lots.
Vi-JonJul 17, 2017 - Lower riskFood
NatureBox, Inc. recalls NatureBox Sticks 'n Stones; roasted nuts with sesame sticks. Packed in 5 oz. pouch and 5 lb. corporate bag
NatureBox recalls roasted nut snacks containing cashews and almonds after a consumer found a peanut in the product. This poses a risk for people with peanut allergies.
NatureBoxJul 17, 2017 - Stop using nowMeat & poultry
Marathon Enterprises Inc. Recalls Hot Dog Products Due to Possible Extranous Material Contamination
Marathon Enterprises recalls ~7.2M lbs of hot dogs due to possible bone fragment contamination. Do not consume; discard or return items.
SABRETTJul 15, 2017 - Use cautionMeat & poultry
Custom Culinary, Inc. Recalls Chicken and Beef Products Due to Misbranding and Undeclared Allergens
USDA FSIS recalls 9,444 lbs of chicken/beef soup bases due to mislabeling as chicken but containing beef and undeclared soy allergen. Consumers urged to stop using these products.
Custom CulinaryJul 14, 2017 - Use cautionVehicle
SMART FORTWO (2017) recall — Steering
Mercedes-Benz USA recalls 2017 Smart Fortwo vehicles with potential left front axle steering knuckle failure that could cause crashes. Owners must have steering knuckle inspected and replaced free by dealers.
SmartJul 14, 2017 - Lower riskVehicle
FOREST RIVER ROCKWOOD (2017) recall — Equipment
Forest River is recalling certain 2017 Rockwood travel trailers with an incorrect VIN check digit that may cause improper licensing and failure to account for the vehicle in safety recalls.
Forest RiverJul 14, 2017 - Use cautionMedical device
Mindray DS USA, Inc. dba Mindray North America recalls TD60 Transmitter battery charger used with the BeneVision Central Station, Part number 115-030108-00
Mindray recalls TD60 Transmitter battery chargers (part 115-030108-00) due to risk of battery swelling and separation. Affected units may need replacement.
MindrayJul 14, 2017 - Use cautionMedical device
Philips Electronics North America Corporation recalls Mobile Detector Holder - Stationary X-ray System (RF System). suitable for positioning the wireless portable detector
Philips recalls mobile detector holders for stationary X-ray systems (RF) due to risk of portable X-ray detector dropping when rotated. Affected units manufactured March 2015-March 2017.
PhilipsJul 14, 2017 - Lower riskMedical device
Panoramic Rental Corp. recalls PC-1000, PC-1000/Laser1000, Model Numbers 800724-2 & 800724-3
Panoramic Rental Corp. recalls PC-1000 and PC-1000/Laser1000 models with serial numbers 6001-19340 due to lift motor wear from improper maintenance. Affected users should contact the company for details.
Panoramic Rental Corp.Jul 14, 2017 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls A-Series A7 Anesthesia Delivery System; Model Number: 0632F-PA0000X (A7) Product Usage: The A-Series Anesthesia System
Mindray recalls A7 Anesthesia Delivery System model 0632F-PA0000X (2013-2016) due to software error potentially skipping startup leak test. Affected units may apply wrong settings during anesthesia delivery.
MindrayJul 14, 2017 - Lower riskMedical device
Fujifilm Medical Systems U.S.A., Inc. recalls ASPIRE Cristalle (FDR MS-3500) Mammography machine The Fujifilm Digital Mammography Systems, Aspire HD Plus (FDR
Fujifilm recalls ASPIRE Cristalle mammography machines with serial numbers 76221095 or earlier due to risk of unintended swivel arm movement during operation. Affected units may require repair or replacement.
FujifilmJul 14, 2017 - Use cautionMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure recalls MyCareLink Smart Patient Monitors. It is intended for use with a compatible Medtronic patient implanted heart device.
Medtronic recalls MyCareLink Smart Patient Monitors used with implanted heart devices. These monitors may miss critical heart device alerts, risking missed CareAlert notifications for patients with two or more implanted devices.
MedtronicJul 14, 2017 - Lower riskMedical device
Leica Biosystems Richmond Inc. recalls Cell Marque, PAX8 (MRQ-50 Mab.), 7 mL, REF PA0808, IVD, This antibody is intended for in vitro diagnostic (IVD) use.
Leica Biosystems recalls PAX8 (MRQ-50) antibody products due to potential temperature storage issues affecting lab diagnostics. This may impact accuracy of IHC testing if stored outside recommended conditions.
Leica BiosystemsJul 14, 2017 - Stop using nowDrug
SCA Pharmaceuticals recalls Diltiazem 125 mg in 0.9% Sodium Chloride, 1 mg per mL, Total Volume 125 mL Single Dose Container bag, Rx Only, SCA
SCA Pharmaceuticals recalls Diltiazem 125mg in 0.9% sodium chloride bags due to potential leakage. This could compromise sterility and safety. Affected units have specific NDC and lot numbers.
SCA PharmaceuticalsJul 14, 2017 - Lower riskDrug
Cantrell Drug Company recalls Phenylephrine HCL in 0.9% Sodium Chloride 10 mL, 1 mg/10 mL (100 mcg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug
Cantrell Drug Company recalls phenylephrine HCl in 0.9% sodium chloride syringes (NDC 52533-171-12) due to lack of sterility assurance. This may cause infections if used improperly.
Cantrell DrugJul 14, 2017 - UnratedDrug
SCA Pharmaceuticals recalls PHENYLephrine 40 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205
SCA Pharmaceuticals recalls PHENYLephrine 40mg in 0.9% Sodium Chloride 250mL (Rx only) due to potential contamination and leakage risks. Affected units have specific lot numbers and expiration dates.
SCA PharmaceuticalsJul 14, 2017 - Lower riskFood
Garden Of Light Inc. recalls WOODSTOCK ORGANIC MATCHA VANILLA OATS, 1.8 oz (50g) cup UPC: 0-42563-01786-6
Garden Of Light recalls organic matcha vanilla oats due to potential Listeria contamination in specific lot codes from May and June 2018. Consumers should check their product codes and take action if affected.
Garden Of LightJul 14, 2017 - Lower riskFood
The Idaho Foodbank recalls Signature Caf¿ Broccoli & Cheesy Cheddar Soup, 24 oz. plastic tub.
The Idaho Foodbank recalls 24oz Signature Caf¿ Broccoli & Cheesy Cheddar Soup due to improper temperature storage causing potential food safety risks.
The Idaho FoodbankJul 14, 2017 - Use cautionVehicle
KEYSTONE OUTBACK (2017) recall — Structure
Keystone is recalling 2016-2017 Outback travel trailers with a faulty drawbar that may bend under certain conditions, increasing crash risk. Owners must have the reinforcement channel bolted on.
KeystoneJul 13, 2017 - Use cautionVehicle
HONDA CR-V (2017) recall — Fuel System, Gasoline
Honda is recalling certain 2017 CR-V models due to a fuel supply pipe that may disconnect while driving, causing engine stalling and potential fuel leaks that could lead to fire.
HondaJul 13, 2017 - Use cautionVehicle
KENWORTH T680 (2018) recall — Fuel System, Diesel
PACCAR recalls 2018 Kenworth T680 trucks with Cummins ISX 15L engines due to potential fuel pump failure causing engine stalls. Owners should contact PACCAR for free fuel pump replacement.
PACCARJul 13, 2017
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83,389 recalls tracked · 71,917 explained in plain English · 10,946 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.