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
IC BUS CESB (2016) recall — Electrical System
Navistar recalls certain 2016-2019 IC school buses with propane engines due to risk of fuel pump stalling and potential crashes. Owners must contact Navistar for free relay replacement.
NavistarFeb 20, 2018 - Use cautionVehicle
TOYOTA TUNDRA (2017) recall — Seats
Toyota recalls 2017 Tundra vehicles with rear split bench seats that may move in crashes, increasing injury risk. Owners must have seat leg brackets tightened by dealers.
ToyotaFeb 20, 2018 - Use cautionVehicle
TOYOTA SEQUOIA (2018) recall — Electronic Stability Control (Esc)
Toyota recalls 2018 Sequoia vehicles with potential electronic stability control deactivation, risking crashes. Owners must update software free via dealer by March 14, 2018.
ToyotaFeb 20, 2018 - Use cautionMedical device
Deerfield Imaging, Inc. recalls IMRIS T2X Table, Part Number 109682-600
Deerfield Imaging recalls IMRIS T2X surgical tables with serial numbers listed. The rotational locking may disengage during use, causing unintended table movement. Affected users should contact for remedy.
Deerfield ImagingFeb 20, 2018 - Lower riskMedical device
Cardinal Health 200, LLC recalls Presource PBDS, Kit, Common. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG,
Cardinal Health recalls Presource PBDS kits with leaking Gatorade pouches that could cause skin irritation during surgery preparation. Affected kits include specific product codes and lot numbers.
Cardinal HealthFeb 20, 2018 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Syngo.plaza software VB10A model numbers: 10863171, 10863172, 10863173 Syngo.Plaza is a Picture Archiving and
Siemens recalls Syngo.plaza software VB10A model numbers 10863171-10863173 due to potential patient misdiagnosis from incorrect study date formats and legacy presentation states. Affected healthcare facilities should contact Siemens for remediation.
SiemensFeb 20, 2018 - Stop using nowDrug
Hospira Inc. A Pfizer Company recalls Labetalol Hydrochloride Injection, USP, 100 mg/ 20 mL (5 mg/mL), 20 mL Multidose Vial, Rx only, labeled as a) Hospira,
Hospira recalls labetalol injection vials with cracked glass rims that could lead to contamination. Affected lots and NDCs listed; stop using immediately.
HospiraFeb 20, 2018 - Lower riskFood
Market of Choice Inc recalls Sezam Kale Salad ingredient kits, net wt. 6.43 pound. Ingredients are packaged individually and then placed in one
Market of Choice recalls Sezam Kale Salad ingredient kits (6.43 lbs) due to undeclared egg in dressing. Products sold with UPC 2 11565 20216 1 and production codes 02-14-18 or 02-15-18.
Market of ChoiceFeb 20, 2018 - Lower riskFood
Bob's Red Mill Natural Foods, Inc. recalls Buttermilk Pancake and Waffle Mix, Item number: 6170B25, packaged in 25 lbs. bulk kraft bag. The label is read in
Bob's Red Mill recalls Buttermilk Pancake and Waffle Mix (Item 6170B25) due to incorrect labeling with undeclared milk. Consumers should check labels for the listed lot codes and expiration dates.
Bob's Red MillFeb 20, 2018 - Lower riskFood
Lotte International America Corp. recalls Lotte Kancho Choco-Biscuit; Sold as Lotte Kancho - 42 g -1.48 oz. UPC CODE: 8801062 144815; Lotte Kancho Cup - 95 g cup
Lotte International America Corp. recalls Lotte Kancho Choco-Biscuits due to peanut allergen detected in product sampling. Consumers should check UPC codes and avoid if allergic to peanuts.
Lotte KanchoFeb 20, 2018 - Stop using nowFood
Margalaxy LLC recalls Cosmic Crunch Granola, packaged in paper bag, net wt 10 oz. The product is labeled in parts: "***COSMIC CRUNCH
Margalaxy LLC recalls Cosmic Crunch Granola due to undeclared coconut. Check your package for specific best-by dates and discard if affected.
MargalaxyFeb 20, 2018 - Stop using nowConsumer product
Whirlpool Recalls KitchenAid Electric Kettles Due to Burn Hazard
KitchenAid recalls electric kettles due to burn hazards. Stop using immediately and contact Whirlpool for a free replacement if you have affected models.
KitchenAidFeb 20, 2018 - Stop using nowConsumer product
NEMO Equipment Recalls Stargaze Recliner Chairs Due to Fall Hazard; Sold Exclusively at REI
NEMO Equipment recalls Stargaze Recliner chairs due to fall hazard from failing straps. Consumers must stop using and get a free replacement.
NEMO EquipmentFeb 20, 2018 - Use cautionVehicle
CROSSROADS ZINGER (2018) recall — Electrical System
Keystone is recalling 2018 Crossroads Zinger RVs with a potential electrical short that could cause fire. Owners must have their GFCI receptacle inspected by dealers for proper ground wire connection.
KeystoneFeb 19, 2018 - Use cautionVehicle
THOR MOTOR COACH OUTLAW (2019) recall — Seat Belts
Thor Motor Coach is recalling 2018-2019 Outlaw RVs with seat belt brackets that may fail in crashes, risking injury. Owners must have a new bracket installed by dealers.
Thor Motor CoachFeb 19, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls EBI Osteogen Implantable Bone Growth Stimulator The OsteoGen Implantable Bone Growth Stimulator is indicated in the
Zimmer Biomet recalls OsteoGen implantable bone growth stimulators with serial numbers expiring before March 31, 2019 due to lack of validation for product cleanliness.
Zimmer BiometFeb 19, 2018 - Lower riskDrug
Kalchem International, Inc. recalls Vardenafil HCl, USP (trihydrate), 500 GM Part # 330-05, Rx only, For Manufacturing, Repackaging and Processing for Rx
Kalchem International recalls Vardenafil HCl 500mg (NDC 60592-330-05) due to insufficient stability data affecting expiration dates. Consumers should contact the manufacturer for details.
KalchemFeb 19, 2018 - Stop using nowFood
Ventura Foods, LLC recalls Gordon Choice Asian Sesame Ginger Dressing, Net Contents/Contenido Neto 128 FL OZ; For Distribution Exclusively By
Ventura Foods recalls Gordon Choice Asian Sesame Ginger Dressing due to blue plastic contamination. Check your jugs for lot codes B29717 and B01018.
Gordon ChoiceFeb 19, 2018 - Use cautionVehicle
HYUNDAI SANTA FE (2018) recall — Steering
Hyundai is recalling certain 2018 Santa Fe vehicles due to potential steering wheel separation while driving, which could cause loss of vehicle control and increase crash risk. Owners should contact customer service for free replacement.
HyundaiFeb 17, 2018 - Use cautionMeat & poultry
Pilgrim's Pride Corporation Recalls Ready-to-Eat Chicken Products due to Possible Foreign Matter Contamination
USDA recalls 101,310 pounds of Pilgrim's Pride ready-to-eat chicken patties that may contain rubber. Consumers are urged not to eat these products and should discard or return them.
Pilgrim's PrideFeb 16, 2018 - Lower riskMedical device
Aesculap Implant Systems LLC recalls Strauss Penis Clamp 130MM/General Instruments
Aesculap recalls Strauss Penis Clamp 130MM/General Instruments due to plastic sleeves sticking during reprocessing, making instruments unusable after reprocessing. Affected units include model EF401R.
Aescul: Aesculap Implant Systems LLCFeb 16, 2018 - Lower riskDrug
B. Braun Medical Inc recalls 0.9% Sodium Chloride Irrigation USP, 1000 mL Plastic Irrigation Container (PIC), Rx only, B. Braun Medical Inc.,
B. Braun Medical recalls 1000mL plastic irrigation containers due to reported polyethylene particles. This may cause blockages or infections. Affected units have specific batch numbers and expiration dates.
B. Braun MedicalFeb 16, 2018 - Lower riskFood
Bob's Red Mill Natural Foods, Inc. recalls Organic Creamy Wheat Hot Cereal, Item number 6097C244, Pack size: 24 oz bag, 4 bags in a case. UPC: 3997800992
Bob's Red Mill recalls 24oz Organic Creamy Wheat Hot Cereal (UPC 3997800992) due to wheat not being declared on back label despite front label showing organic wheat. Consumers should check labels for 'Outrageous Muffins' label.
Bob's Red MillFeb 16, 2018 - Lower riskFood
Double-Cola Co.-USA dba The Double Cola Company recalls Cherry SKI LEMON ORANGE AUTHENTIC CITRUS SODA 12 oz can CONTAINS: CARBONATED WATER, HIGH FRUCTOSE CORN SYRUP, LEMON
The Double Cola Company recalls Cherry SKI Lemon Orange Authentic Citrus Soda 12oz cans due to missing allergen labels for Yellow 5 and Red 40. Consumers should check product codes and contact the company for details.
The Double Cola CompanyFeb 16, 2018 - Lower riskFood
M & P Food Productions, Ltd. recalls M&P Food Productions brand Vareniki Cabbage, Net WT 14 oz. (396g), Keep Frozen, UPC: 7 07163 02619 8
M&P Food Productions recalls 14oz Vareniki Cabbage due to undeclared wheat. Consumers should check UPC 707163026198 and use by dates 02/16/2018 - 08/15/2018.
M&P Food ProductionsFeb 16, 2018 - Use cautionVehicle
MERCEDES-BENZ SPRINTER 2500 (2017) recall — Equipment
Daimler Vans USA recalls 2016-2017 Mercedes-Benz Sprinter 2500 vehicles with incorrect UVW labels that could cause vehicle overload and crash risk. Owners must have label replaced by dealers at no cost.
Mercedes-BenzFeb 15, 2018 - Use cautionVehicle
JAGUAR XF (2018) recall — Air Bags
Jaguar is recalling 2018 XF Sportbrake vehicles with potentially incorrect air bag calibration that could cause improper deployment in low speed crashes. Owners will receive free software updates starting April 6, 2018.
JaguarFeb 15, 2018 - Lower riskMedical device
Philips Medical Systems (Cleveland) Inc recalls Ingenuity TF PET/CT, Model No. 882442 Product Usage: The device is an integrated diagnostic X-ray Computed Tomography
Philips recalls specific model Ingenuity TF PET/CT systems due to potential unresponsiveness after inactivity. Affected units may not complete scans. No remedy stated in recall notice.
PhilipsFeb 15, 2018 - UnratedMedical device
Ra Medical Systems Inc recalls The DABRA Laser (model RA-308) is designed to provide ultraviolet laser energy endovascularly through a catheter to
Ra Medical Systems recalls DABRA Laser (model RA-308) due to potential laser calibration errors during setup, which could affect medical procedures. Affected units have specific serial numbers.
Ra Medical SystemsFeb 15, 2018 - Lower riskMedical device
Teleflex Medical recalls Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.
Teleflex Medical recalls Visistat 35 devices where some boxes contain regular devices labeled as wide. This affects laceration closure products.
Teleflex MedicalFeb 15, 2018
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