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
34,894 found- Use cautionVehicle
JEEP COMPASS (2018) recall — Suspension
Chrysler recalls certain 2018 Jeep Compass vehicles with potentially incorrectly welded front lower control arms that could separate, causing loss of vehicle control and crash risk.
ChryslerJan 5, 2018 - Use cautionVehicle
DODGE CHARGER (2018) recall — Power Train
Chrysler recalls certain 2015-2018 Dodge Charger police vehicles with AWD and V8 engines due to risk of front driveshaft detachment causing crashes.
ChryslerJan 5, 2018 - Use cautionVehicle
CHRYSLER 300 (2018) recall — Power Train
Chrysler recalls 2018 300 vehicles with incorrect park lock rod that may prevent shifting into park, risking unintended movement and crashes. Owners must contact Chrysler for free fix.
ChryslerJan 5, 2018 - Use cautionMedical device
ICU Medical, Inc. recalls Hemodynamic monitoring system (HMS), comprised of a Patient Interface Module (Part Number 58401-000 and a User
ICU Medical recalls hemodynamic monitoring systems with Patient Interface Module (58401-000) and User Interface Module (58403-000) that may continue thermal coil activity when paused, potentially causing overheating.
ICU MedicalJan 5, 2018 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls AXIOM Artis angiographic x-ray system, Model Numbers: 7412807, 7413078, 7728392 AXIOM Artis is a family of dedicated
Siemens recalls specific AXIOM Artis angiography systems due to potential coolant leaks that could damage the imaging detector. Affected models include 7412807, 7413078, 7728392. Patients may need to cancel procedures or switch systems.
Siemens Medical SolutionsJan 5, 2018 - Lower riskMedical device
Diamedix Corporation recalls Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-540
Diamedix recalls Is-Mumps IgG Enzyme Immunoassay Test Kit (Catalog No. 720-540) due to gel-like contaminant that may affect test accuracy. Affected lots: S0406, expiring 05/31/2018.
DiamedixJan 5, 2018 - Lower riskDrug
Advanced Pharma Inc. recalls MAGnesium 2 gm in NS 100 mL Magnesium SULfate (USP) 0.9% Sodium Chloride (USP) in 100 mL Sterile single dose bag, Rx
Advanced Pharma recalls magnesium sulfate solution (NDC 42852-907-10) due to subpotent risk. This medication is for prescription use only and may not contain enough active ingredient.
Advanced PharmaJan 5, 2018 - Stop using nowFood
H.I.G. Corporation recalls Frozen Tuna Fillet Saku (Restaurant Supply Only); 22 lbs./2 x 5 kgs. Wild caught: Handline with Hook. Keep Frozen - 18
H.I.G. Corporation recalls frozen tuna fillets sold to restaurants due to Listeria monocytogenes found in customer testing. Product was wild-caught from Indonesia and sold with specific temperature requirements.
H.I.G. CorporationJan 5, 2018 - Lower riskFood
Mom's Delicious Kitchen LLC recalls Kvas, a fermented non-alcoholic drink, packaged in a gallon plastic jugs The label is read in parts: "***Mom's Kvas***1
Mom's Delicious Kitchen LLC recalls gallon plastic jugs of fermented non-alcoholic Kvas due to bulging from compromised packaging. Consumers should check for bulging jugs and contact the company for details.
Mom's KvasJan 5, 2018 - Use cautionMeat & poultry
Hempler Foods Group, LLC Recalls Pepperoni Products due to Possible Extraneous Material Contamination
Hempler Foods recalls pepperoni sticks from Oct. 2017 due to possible metal contamination. Consumers are urged not to eat these products and should discard or return them.
Hempler FoodsJan 4, 2018 - Lower riskMedical device
The Binding Site Group, Ltd. recalls Rheumatoid Factor (RF) Kit for use on SPAPLUS, Product #LK151.S.A Intended for the quantitative in-vitro measurement of
The Binding Site Group recalls Rheumatoid Factor (RF) Kit for SPAPLUS analyser due to low and high controls returning results above assigned values. This may affect rheumatoid arthritis testing accuracy.
The Binding Site GroupJan 4, 2018 - Use cautionMedical device
Toshiba American Medical Systems Inc recalls Diagnostic Ultrasound System, Aplio I-series. Labeled as i700, i800, i900 The power supply unit may be damaged and may
Toshiba recalls Aplio i700, i800, i900 ultrasound systems where the power supply may fail to start when plugged in with the main switch set to ON. Affected units have specific model and serial numbers.
ToshibaJan 4, 2018 - Lower riskMedical device
bioMerieux, Inc. recalls BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usage: the Quality Control VIDAS
BioMerieux recalls Quality Control VIDAS (QCV) systems due to pump clogging and label displacement causing inaccurate test results. Affected lab equipment may need replacement to ensure reliable diagnostic testing.
BioMerieuxJan 4, 2018 - Use cautionMedical device
Philips Electronics North America Corporation recalls Allura Xper systems with Certeray X-ray Generator located in regions with high mains (480V) voltage. Product Usage: The
Philips recalls Allura Xper systems with Certeray X-ray Generators in 480V regions due to risk of overheating and reduced X-ray performance from early ADU5 failures.
PhilipsJan 4, 2018 - Lower riskDrug
International Laboratories, LLC recalls Clopidogrel Tablets, USP 75 mg, 30-count bottles, Rx only, Packaged for: International Laboratories, LLC St.
International Laboratories recalls 75mg Clopidogrel tablets that were mislabeled with simvastatin 10mg. This mix-up could lead to incorrect medication use.
International LaboratoriesJan 4, 2018 - Lower riskFood
Ventura Foods Llc recalls SunGlow, Unsalted European Style Butter Blend Margarine (16953 SNG), Net Wt 16 oz (1 lb) 454 g. Keep Refrigerated. UPC
Ventura Foods recalls SunGlow Unsalted European Style Butter Blend Margarine due to undeclared soy lecithin. This may cause allergic reactions in sensitive individuals. Check product details and contact for remedy.
Ventura FoodsJan 4, 2018 - Lower riskFood
Dollar General Corporation, Inc. recalls Clover Valley¿ Iced Oatmeal Cookies NET WT 12 OZ (340 g) CONTAINS: WHEAT, SOY. DISTRIBUTED BY DOLGENCORP, LLC 100
Clover Valley Iced Oatmeal Cookies (12 oz) recalled for mislabeling that hides tree nuts and milk in ingredients. Consumers should check for hidden tree nuts and milk.
Clover ValleyJan 4, 2018 - Stop using nowConsumer product
SureFit Recalls Riding Lawn Mower Blade Spindle Shafts Due to Impact Hazard (Recall Alert)
SureFit recalls riding lawn mower blade spindle shafts (models 504-00341 and 504-00346) due to risk of broken blades causing impact injuries. Consumers must stop using and contact for free replacement.
SureFitJan 4, 2018 - Use cautionConsumer product
HP Recalls Batteries for Notebook Computers and Mobile Workstations Due to Fire and Burn Hazards
HP recalls lithium-ion batteries for notebook computers and mobile workstations due to fire and burn risks. Affected batteries may overheat and cause injury. Consumers should check HP.com for recall details and enable Battery Safety Mode.
HPJan 4, 2018 - Use cautionVehicle
LAND ROVER RANGE ROVER VELAR (2018) recall — Visibility
Land Rover recalls 2018 Velar vehicles where ventilation system may not clear fog or condensation, risking driver visibility. Owners must update software to fix issue.
Land RoverJan 3, 2018 - Use cautionVehicle
FORD TAURUS (2018) recall — Electrical System
Ford is recalling certain 2018 Taurus vehicles with mechanical key ignitions that may roll away if key is removed while not in park and parking brake not applied. Owners must contact Ford for free shifter assembly replacement.
FordJan 3, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Trabecular Metal¿ Primary Hip Prosthesis; Part Numbers: 1. 00-7864-013-00 (UDI: (01) 00889024139251 (17) 250731 (10)
Zimmer Biomet recalls two lots of hip implants due to mislabeling. Affected products may have incorrect part numbers or lot codes. Consumers should check their implant details against the provided identifiers.
Zimmer BiometJan 3, 2018 - Use cautionMedical device
Teleflex Medical recalls Percuvance(R) Percutaneous Shaft 36cm, PCVSHL3 The Percutaneous Surgical System with 5mm attachments is indicated for
Teleflex Medical recalls Percuvance 36cm surgical shafts with specific batch numbers due to potential tip breakage during laparoscopic procedures, requiring surgical intervention if broken.
Teleflex MedicalJan 3, 2018 - Lower riskMedical device
Philips Medical Systems (Cleveland) Inc recalls Brilliance Big Bore Oncology CTwith 4.2.0 software version. Model #' 728243 Product Usage: Computed Tomography X-ray
Philips recalls specific models of Brilliance Big Bore Oncology CT scanners due to software errors that may cause image generation failures or incorrect scans. Affected units have model # 728243 and serial numbers listed. No remedy is stated in the recall notice.
Philips Medical SystemsJan 3, 2018 - Use cautionMedical device
ESAOTE S.P.A. recalls MyLab Ultrasound System; Models 6100, 6150, 6200, 6250; Probes: BL433, C 18, CA541, EC1123, EC123, IH 618, IOT332,
ESAOTE recalls specific MyLab ultrasound models due to potential probe overheating. Affected units include models 6100-6250 and listed probes. Contact ESAOTE for details.
ESAOTEJan 3, 2018 - Use cautionMedical device
Philips Electronics North America Corporation recalls Intellivue iX Information Center Software - All PIIC iX Surveillance stations including: 866023 IntelliVue Info Center
Philips recalls Intellivue iX surveillance stations that may lose patient monitoring if restarted after January 1, 2018. Users should avoid restarting these stations in 2018 to prevent temporary loss of monitoring.
PhilipsJan 3, 2018 - Lower riskMedical device
GETINGE US SALES LLC recalls HEMASHIELD Knitted Double Velour Cardiovascular Fabric
GETINGE recalls HEMASHIELD Knitted Double Velour Cardiovascular Fabric due to mislabeling. The product's packaging states 2.5cm x 7.6cm but actual size is 2.5cm x 15cm. No remedy specified.
GETINGEJan 3, 2018 - Lower riskMedical device
Medtronic Perfusion Systems recalls Medtronic Custom Perfusion Systems, indicated for use in the extracorporeal circuit during cardiopulmonary bypass (CPB)
Medtronic recalls custom perfusion tubing packs with Terumo OPS valves that may lack flow during cardiopulmonary bypass surgery. Affected units have specific lot/serial numbers listed in the recall.
MedtronicJan 3, 2018 - Lower riskDrug
AVKARE Inc. recalls Lovastatin Tablets USP, 40 mg, 50 Tablets (5x10) Unit Dose carton, Rx only, Manufactured for AvKARE, Inc. Pulaski, TN
AVKARE recalls 40mg Lovastatin tablets with failed dissolution testing. Consumers should contact manufacturer for details.
AVKAREJan 3, 2018 - Lower riskFood
Paris Foods Corporation recalls Seasoning Blend- S.E. Meats (Diced red peppers, green peppers, celery and onions) Net weight 1300 LB in TOTE (Plastic
Paris Foods Corporation recalls Seasoning Blend- S.E. Meats due to potential chemical pesticide residue contamination. Consumers should avoid using this product to prevent health risks.
Paris Foods CorporationJan 3, 2018
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