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- Lower riskFood
Progressive Laboratories, Inc recalls Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap
Progressive Laboratories recalls Thyroid Resilience 120-count supplements with amber plastic bottles and black caps due to potential undeclared milk content. Consumers should check lot numbers 2114667 and 2061167.
Progressive LaboratoriesFeb 23, 2018 - Use cautionVehicle
JEEP RENEGADE (2017) recall — Engine And Engine Cooling
Chrysler recalls certain 2017 Jeep Renegade vehicles with a 2.4L engine that may have a cracked oil pump housing. This could cause engine stalling and increase crash risk. Owners should contact Chrysler for free repairs.
ChryslerFeb 22, 2018 - Use cautionVehicle
WINNEBAGO REVEL (2018) recall — Equipment
Winnebago is recalling 2018 Revel RVs with potential luggage rack detachment risk. Cracked mounting brackets could cause detachment during driving, increasing crash risk. Owners must contact Winnebago for free bracket replacement.
WinnebagoFeb 22, 2018 - Use cautionVehicle
TOYOTA SIENNA (2018) recall — Wheels
Toyota recalls 2018 Sienna vehicles with specific 10-spoke alloy wheels that may crack and separate, causing loss of vehicle control. Owners must have wheels inspected and replaced if needed.
ToyotaFeb 22, 2018 - Use cautionVehicle
RAM PROMASTER CITY (2018) recall — Equipment
Chrysler recalls 2018 RAM ProMaster City vehicles with incorrect tire placards that may allow unsafe occupant numbers, risking tire failure and crashes. Owners must get corrected placards installed.
ChryslerFeb 22, 2018 - Lower riskMedical device
Roche Diagnostics Corporation recalls cobas b 221 AutoQC Module Complete; Catalog numbers: 3313522001 and 3313522692 The Roche Diagnostics Omni S Analyzer is
Roche recalls Omni S Analyzer AutoQC Module Complete (catalogs 3313522001, 3313522692) due to software failure preventing scheduled quality control tests. This may affect test accuracy in critical care labs.
RocheFeb 22, 2018 - Lower riskDrug
SCA Pharmaceuticals, LLC. recalls labetalol HCl injection 20 mg/4 mL (5mg/mL), 4 mL syringe, Rx Only, for IV Use, SCA Pharmaceuticals, Windsor, CT 06095
SCA Pharmaceuticals recalls labetalol HCl injection 4 mL syringes with incorrect lot numbers and expiration dates that could lead to medication errors.
SCA PharmaceuticalsFeb 22, 2018 - Lower riskFood
Ikea North America Srvcs Inc recalls Pink flexible, plastic package: Godis Paskkyckling Marshmallow Candy; IKEA; Net Wt. 3.5 oz.; date codes: 10/23/2018 -
IKEA recalls pink flexible plastic marshmallow candy with possible pest contamination. Products produced in Sweden from 10/23/2018 to 01/26/2019 may contain pests.
IKEAFeb 22, 2018 - Use cautionConsumer product
Yamaha Recalls Golf Cars and Personal Transportation Vehicles Due to Crash Hazard (Recall Alert)
Yamaha recalls 2015-2018 golf cars and PTVs due to brake cable failure causing crash hazards. Affected models have specific serial numbers; contact a dealer for free repair.
YamahaFeb 22, 2018 - Stop using nowConsumer product
Monster Moto Recalls Mini Bikes Due to Fire Hazard
Monster Moto recalls Classic 212cc mini bikes with a fire hazard due to fuel tank venting system leaks. Owners must stop using and get a free repair kit.
Monster MotoFeb 22, 2018 - Use cautionMeat & poultry
Triple T Specialty Meats Inc. Recalls Chicken Salad Products Due to Possible Salmonella Contamination
USDA recalls 20,630 lbs of Triple T chicken salad products from Jan 2018 with possible Salmonella Typhimurium contamination. Consumers urged to discard items purchased from Fareway stores in Iowa, Illinois, Minnesota, Nebraska, and South Dakota.
Triple T Specialty MeatsFeb 21, 2018 - Use cautionMeat & poultry
A & A Finest Recalls Frozen Pork and Shrimp Dumpling Products due to Misbranding and an Undeclared Allergen
A & A Finest recalls frozen pork and shrimp dumplings due to misbranding and an undeclared egg allergen. Consumers are urged not to consume these products.
A & A FinestFeb 21, 2018 - Lower riskMedical device
Echopixel, Inc. recalls True 3D Viewer, Model: EP-00003
Echopixel recalls True 3D Viewer model EP-00003 with certain software versions that may display ultrasound images incorrectly, risking misdiagnosis or incorrect surgery.
EchopixelFeb 21, 2018 - Use cautionMedical device
Draegar Medical Systems, Inc. recalls Infinity Acute Care System (IACS) Monitoring Solution, Catalog Numbers: MS18841, MS20401, MS20407, MS20724, MS22956,
Draegar recalls Infinity Acute Care System monitoring solutions with catalog numbers MS18841, MS20401, etc. due to potential failure of pressure visual and audible alarms.
DraegarFeb 21, 2018 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls Biograph Horizon, PET/CT System using VJ10A, VJ10B, VJ20A scanners that provide registration and fusion of high
Siemens recalls Biograph Horizon PET/CT systems with VJ10A, VJ10B, VJ20A scanners due to potential waveform sampling issues during cardiac gating exams. Affected units may require firmware updates.
SiemensFeb 21, 2018 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc recalls ADVIA Centaur CA 125II Assay; Cat No. 09427226, SMN 10310443 (1-pack/100 tests); Cat no. 01678114, SMN 10315696
Siemens Healthcare recalls Centaur CA 125II Assay kits with specific lot numbers due to potential over-recovery in patient samples during testing.
Siemens HealthcareFeb 21, 2018 - Lower riskMedical device
Philips Medical Systems (Cleveland) Inc recalls Brilliance 64 with 4.1.7 XX026 software version model number 728231 Product Usage: Computed Tomography X-ray systems
Philips recalls Brilliance 64 CT scanners with specific software version due to failure to initialize low tube current scans. Affected units have serial numbers starting with 9134, 9667, etc. No action needed for safe use.
Philips Medical SystemsFeb 21, 2018 - Stop using nowMedical device
Allen Medical Systems recalls F-T3SYSTEM, T3 (Trumpf Table Top) System The device is a surgical table accessory system used to allow prone
Allen Medical Systems recalls F-T3SYSTEM T3 surgical table systems with serial numbers A166677-A395123 due to rail clamps that may fail during use, risking patient injury.
Allen Medical SystemsFeb 21, 2018 - Lower riskMedical device
Datascope Corporation recalls Intra-Aortic Balloon Catheter Mega 7.5FR 30cc Product Usage: The intra-aortic balloon catheter and accessories are used
Datascope recalls Mega 7.5FR 30cc Intra-Aortic Balloon Catheters due to missing contraindications in instructions. This may lead to unsafe use during counterpulsation therapy.
DatascopeFeb 21, 2018 - Lower riskMedical device
CooperVision Inc. recalls clariti 1 day (-1.25) 90 pack, UV Blocking, 90 silicone hydrogel, daily disposable contact lenses The Clariti 1 Day
CooperVision recalls Clariti 1 Day (-1.25) 90-pack contact lenses due to incorrect expiration date labeling on secondary packaging. Affected units have a foil expiration date of 6/30/2020 and carton expiration date of 6/20/2030.
CooperVisionFeb 21, 2018 - Lower riskMedical device
Hycor Biomedical Inc recalls AUTOSTAT II IgM Rheumatoid Factor, IVD, Part: FGA 05 Product Usage: Rheumatoid Factor IgM ELISA is intended to be
Hycor recalls AUTOSTAT II IgM Rheumatoid Factor test kits due to potential false positive results for Rheumatoid Factor. This may lead to incorrect diagnoses of Rheumatoid Arthritis. Affected kits have lot number 154962.
HycorFeb 21, 2018 - Lower riskDrug
Akorn, Inc. recalls Atropine Sulfate Ophthalmic 1% Solution, USP, 5mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake
Akorn recalls Atropine Sulfate Ophthalm: 5mL bottles with stability issues. This medication may not be safe for use as it failed stability testing.
AkornFeb 21, 2018 - Lower riskDrug
Renaissance Lakewood, LLC recalls Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 200 mg in 100 mL (2 mg/mL), package in 100 mL bags, Rx
Renaissance Lakewood recalls Fluconazole Injection 200mg/100mL due to a label mix-up where 50mL bags were found in 100mL packages. This may cause incorrect dosing in medical use.
Renaissance LakewoodFeb 21, 2018 - Lower riskFood
Snyder's-Lance Inc. recalls Emerald brand Glazed Walnuts; Net WT. 6.5 OZ; Re-sealable pouch
Snyder's-Lance recalls Emerald brand glazed walnuts (6.5 oz) due to undeclared peanuts, almonds, cashews, and pecans. Consumers should avoid these products to prevent allergic reactions.
Snyder's-LanceFeb 21, 2018 - Use cautionFood
La Pasta, Inc. recalls HEINEN'S Potato Gnocchi * Preservative Free * 9 oz. (225 g) in clear film plastic trays
Heinen's Potato Gnocchi (9 oz. preservative-free) recalled due to undeclared milk allergen. Consumers should check lot numbers on clear plastic trays.
Heinen'sFeb 21, 2018 - Lower riskFood
Sunneen Health Foods, LLC recalls Whole Foods Vegan Buffalo Chicken Bites; Net Wt. 9 oz; Expiration Date: 2/27/2018; UPC: 636910500059
Sunneen Health Foods recalls Vegan Buffalo Chicken Bites due to mislabeling as vegan buffalo chicken when they are actually vegan sonoma chicken salad without declared pecans.
Sunneen Health FoodsFeb 21, 2018 - Stop using nowFood
MUNK PACK INC recalls Munk Pack PROTEIN COOKIE PEANUT BUTTER CHOCLATE CHIP NET WT 2.96oz (84g); UPC: 853787005351
Munk Pack recalls peanut butter chocolate chip protein cookies due to mold growth. Check lot numbers and UPC before consuming.
Munk PackFeb 21, 2018 - Use cautionConsumer product
Outdoor Gas Fire Pits Recalled Due to Burn Hazard; Sold Exclusively at Home Depot; Made by Yayi
Yayi's 50,000 BTU outdoor gas fire pits with model G-FTB51057B were recalled due to burn risk when turning off propane tanks. Consumers must contact Yayi for a free heat shield repair kit.
YayiFeb 21, 2018 - Stop using nowConsumer product
Cost Plus World Market Recalls Bleeding Drip Taper Candles Due to Fire Hazard
Cost Plus World Market recalls bleeding drip taper candles due to fire hazard from high flame igniting wax. Return for full refund at any store.
Cost Plus World MarketFeb 21, 2018 - Use cautionMeat & poultry
Night Hawk Frozen Foods, Inc. Recalls Frozen Beef Products Due to Misbranding and Undeclared Allergens
USDA FSIS recalls Night Hawk frozen beef patties and gravy due to undeclared milk allergen. Consumers urged not to eat recalled products.
Night HawkFeb 20, 2018
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