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 cautionVehicle
DUCATI MONSTER 1200 (2019) recall — Power Train
Ducati recalls 2017-2019 Monster 1200 motorcycles with potential shift knob detachment causing gear shifting issues and crash risk. Owners must have shift knob inspected and replaced if needed.
DucatiNov 27, 2018 - Stop using nowMedical device
Medical Action Industries Inc recalls Laparotomy Sponge, XR No Loop, Single-Use, Sterile, 18'' x 18'' pre-washed with bands without handles, 5 sponges/pack,
Medical Action Industries recalls sterile laparotomy sponges that may compromise sterility due to barrier breaches. Affected sponges have model 403 and lot 1806JK305A. Stop using immediately to prevent infection risks.
Medical Action IndustriesNov 27, 2018 - Lower riskMedical device
AROA BIOSURGERY recalls Endoform Dermal Template 2x2, SKU 529312 Product Usage: Endoform Dermal Template is a sterile, single use ovine
AROA BIOSURGERY recalls Endoform Dermal Template 2x2 (SKU 52931: EDT-7I01, EDT-...
AROA BIOSURGERYNov 27, 2018 - Use cautionMedical device
Medtronic Perfusion Systems recalls SUCTION / ANTICOAGULATION ASSEMBLY (a) BTC93 (b) BTC98 Suction and Anticoagulation assemblies are indicated for use
Medtronic recalls suction and anticoagulation assemblies (BTC93/BTC98) with Y-connectors that may tear or crack, causing leaks and blood loss during use. Affected units have specific serial numbers.
Medtronic Perfusion SystemsNov 27, 2018 - Use cautionMedical device
ICU Medical, Inc. recalls ICU Medical, Transpac IV Monitoring Kit With Safeset Reservoir and Blood Sampling Port, 152 cm (60") Tubing, Disposable
ICU Medical recalls Transpac IV Monitoring Kit with Safeset Reservoir and Blood Sampling Port due to risk of pressure tubing separation causing delayed therapy or blood loss, air embolism, or contamination.
ICU MedicalNov 27, 2018 - Lower riskDrug
Glenmark Pharmaceuticals Inc., USA recalls Aprepitant Capsules, USP 40 mg, 1 capsule Unit Blister Pack, Rx Only, Manufactured in India for: Glenmark
Glenmark recalls Aprepitant 40mg capsules due to customer reports of missing capsules in blister packs. Affected units have specific NDC and lot numbers. Consumers should check their packaging for the recall details.
GlenmarkNov 27, 2018 - Lower riskDrug
Teva Pharmaceuticals USA recalls Amlodipine and Valsartan Tablets 5 mg/160 mg, (a) 30-count bottles (NDC 0093-7690-56) & 90-count bottles (NDC
Teva recalls 5 mg/160 mg Amlodipine and Valsartan tablets due to FDA-confirmed NDEA impurity. Stop using affected bottles with specific NDC numbers.
TevaNov 27, 2018 - Stop using nowFood
Sprout Creek Farm, Inc. recalls Sprout Creek Farm Kinkead raw cows' milk cheese semi-firm savory brothy. The product is packaged with an orange label.
Sprout Creek Farm recalls raw cows' milk cheese semi-firm savory brothy with orange label due to potential Listeria monocytogenes contamination. Consumers should avoid consumption.
Sprout Creek FarmNov 27, 2018 - Lower riskFood
Oakhouse Bakery recalls Kwik Trip Granola, Bulk Granola, 09976. Net Wt 20 lbs / 9.1 kg. Manufactured by: Oakhouse Bakery, 2221 Mustang Way,
Oakhouse Bakery recalls bulk granola products due to potential undeclared cashews and almonds. Consumers should check lot numbers and contact the company for details.
Oakhouse BakeryNov 27, 2018 - Lower riskFood
Kwik Trip, Inc. recalls Kitchen Cravings Strawberry Parfait, Net Wt 8.25 oz (234g) Creamy Parfait Base, Strawberries with Sweetened Granola.
Kwik Trip recalls strawberry parfaits that may contain undeclared almond and cashew tree nuts. Consumers should check UPC 39779-18433 for affected products.
Kwik TripNov 27, 2018 - Lower riskFood
Gemini Food Corporation Inc recalls Imperial Taste Fried Garlic, Tu Phi; 24 x 8oz. Item #1763 UPC Code: 741861017638; 24 x 12oz. Item #1762 UPC Code:
Gemini Food Corporation recalls Imperial Taste Fried Garlic products due to undeclared wheat in ingredients. Consumers should check UPC codes 741861017638 and 741861017621 for affected items.
Gemini Food CorporationNov 27, 2018 - Stop using nowConsumer product
Öhlins Recalls Bicycle Forks Sold on Specialized Bicycles Due to Fall and Injury Hazards
Öhlins recalls RXF36 and RXF34 air suspension forks due to fall risks. Stop using affected bikes immediately and contact a retailer for a free repair.
ÖhlinsNov 27, 2018 - Stop using nowConsumer product
Lumber Liquidators Recalls 5-Gallon Buckets Due to Drowning Hazard (Recall Alert)
Lumber Liquidators recalls 5-gallon yellow plastic mixing buckets due to drowning hazard for young children. Buckets lack required safety label warning of drowning risk.
Lumber LiquidatorsNov 27, 2018 - Stop using nowConsumer product
IKEA Recalls Dining Tables Due to Laceration Hazard
IKEA recalls white GLIVARP extendable dining tables with a glass extension that can detach unexpectedly, posing laceration risk. Consumers must stop using and return for refund or replacement.
IKEANov 27, 2018 - Use cautionVehicle
MASERATI GHIBLI (2015) recall — Fuel System, Gasoline
Maserati recalls 2015 Ghibli vehicles with potential fuel leaks that could cause fire. Owners must stop using until fixed by dealers.
MaseratiNov 26, 2018 - Use cautionVehicle
ALFA ROMEO GIULIA (2018) recall — Engine And Engine Cooling
Chrysler recalls 2017-2018 Alfa Romeo Giulia vehicles with GME 280HP engines and AWD for brake fluid leaking onto exhaust, risking fire. Owners must have bracket installed to prevent contact.
ChryslerNov 26, 2018 - Use cautionVehicle
VOLKSWAGEN JETTA (2019) recall — Electrical System
Volkswagen recalls 2019 Jetta models with electrical system issue that may not alert drivers when key is left in ignition, increasing theft or crash risk.
VolkswagenNov 26, 2018 - Use cautionVehicle
BMW F850GS (2019) recall — Engine And Engine Cooling
BMW recalls 2019 F850GS motorcycles due to potential loose engine connecting rods that could cause loss of power and increase crash risk. Affected models were not yet sold as of December 7, 2018.
BMWNov 26, 2018 - Lower riskMedical device
Smiths Medical ASD Inc. recalls ProtectIV¿ Plus Safety IV Catheter, sterile. Packaged in a pouch and than into an inner carton.
Smiths Medical recalls Model 306701 ProtectIV Plus Safety IV Catheter due to potential safety mechanism damage. Affected lots include 3635765-3651082. Consumers should check their catheter packaging for lot numbers.
Smiths MedicalNov 26, 2018 - UnratedMedical device
Howmedica Osteonics Corp. recalls Reliance LITe Nerve Hook Bayoneted, 90, Blunt Tip, REF # 48066103 The blunt probe can be used as a conventional means
Howmedica Osteonics recalls specific Reliance LITe Nerve Hook Bayoneted models due to potential sharp edges causing injury during nerve retraction procedures.
Howmedica OsteonicsNov 26, 2018 - Lower riskDrug
Tris Pharma Inc. recalls infants* IBUPROFEN, Concentrated Ibuprofen Oral Suspension, USP (NSAID), 50 mg per 1.25 mL, Dye-Free Berry Flavor, 0.5
Tris Pharma recalls infants' concentrated ibuprofen oral suspension with potential higher ibuprofen concentration. Consumers should check product labels for specific lot numbers and expiration dates to avoid risks.
Tris PharmaNov 26, 2018 - Lower riskFood
Soom Foods recalls Soom Foods Tahini: Soom Foods Chocolate Tahini, 12 oz. Sweet Tahini Halva Spread (6/case)
Soom Foods is recalling chocolate tahini halva spreads produced between April 7 and May 21, 2018, due to possible Salmonella contamination. Consumers should check product dates and lot numbers.
Soom FoodsNov 26, 2018 - Stop using nowFood
TRES HERMANOS BAKERY recalls Tres Hermanos Bakery Telera and Bolillo Mexican White Bread, 1lb and 2 ounces per pkg
Tres Hermanos Bakery recalls Telera and Bolillo Mexican White Bread due to undeclared milk allergen. Check expiration dates Nov-Dec 2018.
Tres Hermanos BakeryNov 24, 2018 - Use cautionMeat & poultry
Chunwei, Inc. Recalls Meat and Poultry Products Due to Misbranding and Undeclared Allergens and Monosodium Glutamate
USDA FSIS recalls Chunwei meat products due to misbranding and undeclared allergens (soy, wheat, dairy, egg, sesame) and monosodium glutamate (MSG). Consumers urged to stop using recalled items.
ChunweiNov 23, 2018 - Use cautionMedical device
Philips North America LLC recalls HeartStart MRx, Rechargeable Li-Ion (lithium ion battery), REF: M3538A, which is a component of HeartStart MRx
Philips recalls HeartStart MRx defibrillators with defective lithium-ion batteries that may fail to charge or power the device, risking operation during emergencies. Affected units have specific serial numbers and were sold from 2019 to 2021.
PhilipsNov 23, 2018 - Lower riskFood
Achdut recalls Raw Tahini sold under the following brand names: Baron's raw Tahini, 454g, UPC: 816412010083; Soom raw Tahini 220kg (no
Achdut recalls raw tahini products due to potential Salmonella contamination. Affected items include Baron's raw tahini (UPC 816412010083) and Soom raw tahini (various sizes and UPCs). Consumers should check product labels and contact Achdut for details.
AchdutNov 23, 2018 - Use cautionVehicle
INTERNATIONAL LONESTAR (2019) recall — Power Train
Navistar recalls certain 2019 International trucks with specific transmissions due to potential unintended vehicle movement causing crashes. Owners must have TCM recalibrated free by dealers.
NavistarNov 21, 2018 - Lower riskMedical device
Abbott Ireland Diagnostics Division recalls Alinity i Ferritin Reagent Kit, List Number 07P6530 The Alinity i Ferritin assay is a chemiluminescent microparticle
Abbott recalls Alinity i Ferritin Reagent Kit (List 07P6530) due to potential bottle neck damage causing reagent loading failures. Affected units include specific lot numbers from Appendix A.
AbbottNov 21, 2018 - Lower riskMedical device
American Contract Systems, Inc. recalls Bag size #4 Custom Convenience Kits Usage: Surgical convenience kits labeled as the following: a. Tray Name: PACK BASIC
American Contract Systems recalls Bag size #4 Custom Convenience Kits used in surgery that may not have reached complete sterilization. Affected kits include specific tray names and lot numbers.
American Contract SystemsNov 21, 2018 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci Xi Surgical System
Intuitive Surgical recalls da Vinci Xi surgical systems with a manufacturing variation causing persistent error 23087 that may lead to loss of arm functionality during surgery. Affected units include specific model and UDI numbers.
Intuitive SurgicalNov 21, 2018
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83,513 recalls tracked · 71,991 explained in plain English · 10,968 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.