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
35,004 found- Stop using nowFood
Bakkavor Foods USA Inc. recalls chef's recipe MUSHROOM BARLEY SOUP NET WT 16 OZ (1LB) 454g PROUDLY DISTRIBUTED BY: HARRIS TEETER, LLC, MATTHEWS, NC
Bakkavor Foods recalls 16 oz containers of Chef's Recipe Mushroom Barley Soup due to undeclared milk. Check your pantry for affected lots.
Chef's RecipeJan 29, 2020 - Stop using nowConsumer product
Summer Infant Recalls SwaddleMe By Your Bed Inclined Sleepers to Prevent Risk of Suffocation
Summer Infant recalls SwaddleMe By Your Bed Inclined Sleepers due to suffocation risk. Infants may roll from back to stomach or side, leading to fatalities. Consumers should stop using and get a refund.
Summer InfantJan 29, 2020 - Stop using nowConsumer product
Graco Recalls Little Lounger Rocking Seats to Prevent Risk of Suffocation
Graco recalls Little Lounger Rocking Seats due to reported infant suffocation risks from rolling positions. Consumers must stop using and get a refund or voucher.
GracoJan 29, 2020 - Stop using nowConsumer product
Evenflo Recalls Pillo Portable Napper Inclined Sleepers to Prevent Risk of Suffocation
Evenflo recalls Pillo Portable Nappers due to reported infant suffocation risks after rolling. Consumers must stop using and get a refund.
EvenfloJan 29, 2020 - Stop using nowConsumer product
Delta Enterprise Corp. Recalls Incline Sleeper with Adjustable Feeding Position for Newborns to Prevent Risk of Suffocation
Delta recalls incline sleepers with adjustable feeding positions for newborns due to suffocation risk. Consumers must stop using and get a refund or voucher.
DeltaJan 29, 2020 - Lower riskMedical device
Qiagen Sciences LLC recalls QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer designed for rapid thermalcycling and real-time
Qiagen recalls software version 2.3.4 for Rotor Gene Q PCR analyzers that may report false negative results in certain tests, risking treatment suspension or non-initiation of medical treatment.
QiagenJan 28, 2020 - Lower riskMedical device
Medicrea International recalls Pedicle Screws, multiple sizes, Article Nos. B36004525 B36004530 B36004535 B36004540 B36004545 B36004550 B36004555
Medicrea International recalls pedicle screws (article numbers B36004525-B36009560) due to incorrect internal component assembly that may cause tulip head disengagement during surgery.
Medicrea InternationalJan 28, 2020 - Use cautionMedical device
Medtronic, PLC recalls McGRATH X3 Disposable Laryngoscope Blades-used with the McGRATH MAC Video Laryngoscope to aid the intubation of the
Medtronic recalls X3 Disposable Laryngoscope Blades used with MAC Video Laryngoscope due to potential optical performance changes. Affected units have specific serial numbers and lot codes.
MedtronicJan 28, 2020 - Use cautionMedical device
Smith & Nephew, Inc. recalls JOURNEY II UNI RESECTION PREP TRIAL, LEFT MEDIAL/ RIGHT LATERAL - Product Usage: The JOURNEY II Uni Resection Prep
Smith & Nephew recalls JOURNEY II Uni Resection Prep Trial surgical instruments with a spike rail that may disassemble due to an oversized thru-hole. Affected models include sizes 1-10 with specific lot codes.
Smith & NephewJan 28, 2020 - Use cautionMedical device
Breas Medical, Inc. recalls Protective Cover Vivo 55/65 (Used for Vivo 50/65), Part No. 006344. It is an accessory (i.e. protective cover) for the
Breas Medical recalls Protective Cover Vivo 55/65 (for Vivo 50/65 ventilators) due to risk of exhalation valve obstruction. This accessory may cause breathing issues if the outlet hole becomes blocked during use.
Breas MedicalJan 28, 2020 - Lower riskDrug
Graviti Pharmaceuticals Private Limited recalls Atorvastatin Calcium Tablets, USP, 10 mg*, 90-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ
Graviti Pharmaceuticals recalls 10mg Atorvastatin tablets due to customer reports of foreign tablets in some bottles. Affected units may contain 20mg tablets instead of 10mg.
Graviti PharmaceuticalsJan 28, 2020 - UnratedDrug
B AND A TRADING CORPORATION recalls Kushim Tablets (Gushim) 45-count packages, Label in foreign language
FDA recalls Kushim Tablets (Gushim) 45-count packages with foreign language labels due to unapproved ingredients. These products contain cinobufagin, bufalin, and bufotenine without FDA approval.
B AND A TRADING CORPORATIONJan 28, 2020 - Lower riskDrug
Teva Pharmaceuticals USA recalls Tramadol Hydrochloride Tablets USP CIV, 50 mg, packaged in a) 100-count bottles (NDC 0093-0058-01), b) 500-count
Teva Pharmaceuticals recalls 50mg tramadol tablets with incorrect patient instructions that may lead to improper dosing. Affected lots manufactured in Czech Republic for US distribution.
Teva PharmaceuticalsJan 28, 2020 - UnratedDrug
NCS Healthcare of Kentucky Inc recalls Glycopyrrolate Tabs, USP, 1 mg, 30-count unit dose blister card, FOR INSTITUTIONAL USE ONLY, Rx Only, Packaged by
NCS Healthcare recalls 1 mg Glycopyrrolate Tabs for potential impurities that could cause serious harm. This medication is for institutional use only and requires a prescription.
NCS HealthcareJan 28, 2020 - Lower riskFood
Beepas LLC recalls Beepa's Original Goulash Starter, 32 oz. (2 PTS) 946.35ml. UPC 60000-90711
Beepas LLC recalls Beepa's Original Goulash Starter (32 oz) due to undeclared milk. Consumers should check UPC 60000-90711 and avoid use if allergic to milk.
BeepasJan 28, 2020 - Lower riskFood
McCormick & Company, Inc. - Flavor Manufacturing Center recalls Sunny Select Au Jus Gravy Mix 1 OZ pouch (24 pouches per case)
McCormick recalls 24-pouch Sunny Select Au Jus Gravy Mix due to undeclared milk. Consumers should check UPC 717544135500 and best by dates for affected products.
McCormickJan 28, 2020 - Lower riskFood
Corinthian Trading Inc recalls UNCOOKED SWEET POTATO CRUSTED ALASKA POLLOCK NUGGETS 5 LBS 2.26KG DISTRIBUTED BY CORINTHIAN FOODS ST. SIMONS ISLAND, GA
Corinthian Trading Inc recalls uncooked sweet potato crust Alaska pollock nuggets due to customer reports of chicken nuggets being included instead of fish. This affects products distributed in St. Simons Island, GA.
CorinthianJan 28, 2020 - Lower riskFood
IL Nuts recalls Yossef Roasting Co. Handcrafted Nuts Watermelon Seeds; 7oz.
IL Nuts recalls 7oz Watermelon Seeds for missing soy allergen declaration. Consumers should check product labels for soy allergen information.
IL NutsJan 28, 2020 - Lower riskFood
Southern Sisters Gourmet recalls Southern Sisters Gourmet Cheddar Garlic Biscuits, Net Wt 16 oz (453.6 g)
Southern Sisters Gourmet recalls 16 oz Cheddar Garlic Biscuits due to undeclared wheat and yellow dyes. Consumers should check product labels for these allergens.
Southern Sisters GourmetJan 28, 2020 - Lower riskMedical device
Exactech, Inc. recalls Truliant Splined Stem Extension, 18mm x 120mm - Product Usage: The devices are used in a cemented total knee prosthesis
Exactech recalls Truliant Splined Stem Extension implants with a labeling error that shows 17mm x 80mm instead of 18mm x 120mm. This affects cemented total knee prosthesis systems.
ExactechJan 27, 2020 - Use cautionMedical device
Fridababy LLC recalls fridababy SmileFrida the TOOTHHUGGER 18+ months Triple Angle Brush Cleans All Sides at Once
Fridababy recalls SmileFrida ToothHugger brushes for 18+ months that may break from chewing, exposing metal pieces. Owners should stop using and check for damage.
FridababyJan 27, 2020 - Lower riskDrug
Teva Pharmaceuticals USA recalls Methylphenidate hydrochloride Extended-Release ablets USP (CII), 27 mg, 100-count bottle, Rx only, Teva Pharmaceuticals
Teva recalls 27mg Methylphenidate extended-release tablets due to possible missing desiccant, which may cause moisture damage. This is a controlled substance prescription-only product.
Teva PharmaceuticalsJan 27, 2020 - Lower riskDrug
Teva Pharmaceuticals USA recalls Desmopressin Acetate Tablets, 0.1 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories, Inc. Fort
Teva Pharmaceuticals USA recalls 0.1 mg Desmopressin Acetate Tablets due to possible missing desiccant, which may affect product stability. Affected lots expire 03/2020 and 04/2020.
Teva Pharmaceuticals USAJan 27, 2020 - Use cautionMeat & poultry
Amity Packing Company Inc. Recalls Raw Ground Beef Products Due to Possible Foreign Matter Contamination
Amity Packing Company recalls 2,020 pounds of raw ground beef products from Jan. 2020 that may contain clear plastic. Consumers are urged not to eat these items and should discard or return them.
Amity Packing CompanyJan 24, 2020 - Use cautionMeat & poultry
Golden Pearl Trading Corporation Recalls Ready to Eat Imported Siluriformes Products Produced Without Benefit of Import Inspection
USDA FSIS recalls 12,054 pounds of ready-to-eat imported fish products from Singapore that were not inspected before entering the US. Consumers are urged not to eat these products and should discard or return them.
Dandy Food ProductsJan 24, 2020 - Use cautionVehicle
RAM 2500 (2020) recall — Power Train
Chrysler is recalling 2019-2020 RAM 2500 trucks with 68RFE transmissions due to potential transmission fluid leaks that could cause engine fires. Owners must contact customer service for a free repair.
ChryslerJan 24, 2020 - Use cautionVehicle
JEEP WRANGLER (2020) recall — Suspension
Chrysler recalls certain 2020 Jeep Wrangler vehicles due to potential separation of the lower control arm bracket, increasing crash risk. Owners must have axles inspected and replaced if needed.
ChryslerJan 24, 2020 - Use cautionVehicle
FOREST RIVER VENGEANCE (2020) recall — Equipment
Forest River is recalling 2020 Vengeance trailers with incorrect Federal Placards that could cause overloading and loss of control. Owners must get replacement placards free from dealers by January 30, 2020.
Forest RiverJan 24, 2020 - Stop using nowMedical device
bioMerieux, Inc. recalls PREVI Isola Insrument and PREVI Isola Printer spares PSUs (power supply units), P1028888-001 PSU (used in Zebra LP2824
bioMerieux recalls PREVI Isola printer power supply units (PSUs) used in Zebra LP2824 printers that may overheat and cause fire. Affected units have specific date codes and instrument serial numbers.
bioMerieuxJan 24, 2020 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS Pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000 - Product Usage:AXIOM Artis is a family of
Siemens recalls ARTIS Pheno-Interventional Fluoroscopic X-Ray System Model 10849000 due to risk of robotic stand blocking by safety brakes, preventing intended movements during procedures.
SiemensJan 24, 2020
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