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
34,893 found- Use cautionVehicle
ACURA TSX (2012) recall — Air Bags
Honda recalls certain 2012 Acura TSX vehicles with improperly installed passenger air bags that may deploy incorrectly in crashes, increasing injury risk. Owners must have the air bag module replaced free by dealers.
HondaAug 31, 2017 - Use cautionVehicle
TOYOTA LAND CRUISER (2016) recall — Air Bags
Toyota recalls 2016 Land Cruiser air bags that may not deploy in crashes, increasing injury risk. Owners must get free replacement air bags by September 2017.
ToyotaAug 31, 2017 - Use cautionVehicle
MAZDA MAZDA6 (2016) recall — Steering
Mazda recalls 2016 Mazda6 vehicles with potential wiring damage causing loss of power steering and passenger airbag deactivation. Owners must contact Mazda for free repairs to prevent crash risks.
MazdaAug 31, 2017 - Use cautionVehicle
DODGE DURANGO (2017) recall — Power Train
Chrysler recalls 2017 Dodge Durango vehicles with potentially too-short rear axle halfshafts that could cause loss of drive and crash risk. Owners must have halfshafts replaced free by dealers.
ChryslerAug 31, 2017 - Use cautionVehicle
JEEP CHEROKEE (2018) recall — Equipment
Chrysler recalls 2017-2018 Jeep Cherokees with missing tire and rim labels that could lead to incorrect tire installation and crash risk. Owners must get corrected labels.
ChryslerAug 31, 2017 - Use cautionVehicle
CHRYSLER PACIFICA (2018) recall — Seat Belts
Chrysler recalls 2017-2018 Pacifica models with 8-passenger seating for potential seat belt unlatching during crashes. Owners must get free seat belt buckle repair.
ChryslerAug 31, 2017 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Syngo.via systems with SW VB20A
Siemens recalls Syngo.via systems with SW VB20A software update to fix bugs and inconsistent diagnosis issues. Affected units may require software upgrade to VB20A_HF02.
SiemensAug 31, 2017 - Lower riskMedical device
Exactech, Inc. recalls Equinoxe Cage, Glenoid, Alpha, Small Product Usage: The Equinoxe Shoulder System is indicated for use in skeletally
Exactech recalls Equinoxe Shoulder System products with catalog #314-13-03 and serial numbers 5013050-501: potential mislabeling could lead to incorrect use in skeletally mature patients.
ExactechAug 31, 2017 - Lower riskMedical device
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls 1113 Gravity Tube Set Pk/24 -SH Product Usage: The FMS Gravity Tube Set is intended to deliver irrigation fluid from
DePuy Mitek recalls 1113 Gravity Tube Set Pk/24 -SH due to leakage at bulb and tube connection. Affected units have specific lot codes. Contact for remedy.
DePuy MitekAug 31, 2017 - Use cautionMedical device
ICU Medical, Inc. recalls SURPLUG MICRO CONNECTOR Item No. 066-C3352; 111" (282 cm) Appx 13.9 ml, 15 Drop Admin Set w/3-Way Stopcock, 1 Ext, Luer
ICU Medical recalls specific IV sets that may contain a metallic burr in stopcocks, which could cause injury during use. Affected products include various 15-drop admin sets with 3-way stopcocks.
ICU MedicalAug 31, 2017 - UnratedMedical device
Laerdal Medical Corporation recalls LCSU 4, Laerdal Compact Suction Unit The LCSU 4 is a portable, electrically powered, medical suction device intended
Laerdal Medical recalls LCSU 4 suction units that were refused by FDA due to missing approvals. Affected units have serial numbers between 170401A0001 and 170401A0270.
LaerdalAug 31, 2017 - Lower riskMedical device
DePuy Orthopaedics, Inc. recalls DELTA XTEND" Reverse Shoulder System Modular Centered and Eccentric Epiphysis Implants intended for use in total
DePuy recalls Delta XTEND Reverse Shoulder System implants due to potential surgical delay from improper assembly. Affected lots include specific model numbers for shoulder replacement procedures.
DePuyAug 31, 2017 - Lower riskMedical device
Orthoscan, Inc. recalls Mobile Mini C-arm system Part # 1000-0004. Intended to provide the physician with general fluoroscopic visualization of
Orthoscan recalls Mobile Mini C-arm system (Part #1000-0004) due to software allowing digital zoom that exposes patients to higher X-ray radiation than intended. Affected units have specific serial numbers listed in the recall notice.
OrthoscanAug 31, 2017 - Stop using nowDrug
Amneal Pharmaceuticals LLC recalls Fosphenytoin Sodium Injection, USP, 500 mg PE/10 mL (50 mg PE/mL. 10 mL Single Dose Vial, Rx Only. Distributed by:
Amneal Pharmaceuticals recalls 500 mg fosphenytoin sodium injection vials due to particulate matter. This could cause serious injury if injected. Affected vials have specific NDC and lot numbers.
Amne:alAug 31, 2017 - Lower riskFood
Reese Pharmaceutical Company recalls Berry Flavor Immune Support Dietary Supplement Effervescent Tablets 10 Tablets/bottle. Product is sold under the
Reese Pharmaceutical Company recalls Berry Flavor Immune Support Dietary Supplement Efferves: 10 tablets/bottle. The label does not list sodium in ingredients. No remedy provided in recall notice.
Reese Pharmaceutical CompanyAug 31, 2017 - Lower riskFood
Cargill Cocoa and Chocolate, Inc. recalls Shoprite Real Semi-Sweet Chocolate Chips, Net Wt. 24 oz., UPC 41190-02668 best by dates 4-11-2019 and 4-12-2019.
Cargill Cocoa & Chocolate recalls Shoprite Real Semi-Sweet Chocolate Chips (24 oz, UPC 41190-02668) best by 4/11/2019 and 4/12/2019 due to undeclared milk. Consumers should check labels and contact retailer for details.
Cargill CocoaAug 31, 2017 - Stop using nowConsumer product
Hallmark Recalls Plush Baby Stacking Toys Due to Choking Hazard
Hallmark recalls itty bittys baby plush stacking toys due to fabric hats and bows detaching, creating a choking hazard for young children.
HallmarkAug 31, 2017 - Stop using nowMeat & poultry
Demakes Enterprises, Inc. Recalls Chicken Sausage Product Due To Misbranding and Undeclared Allergens
Demakes Enterprises recalls ~32,228 lbs of chicken sausage because labels miss milk allergen. Do not consume; return or discard.
Demakes EnterprisesAug 30, 2017 - Use cautionVehicle
NEW FLYER XD60 (2017) recall — Seat Belts
New Flyer recalls 2017 XD60 buses with Recaro seat belts that may not latch properly, increasing crash injury risk. Owners must contact customer service for free buckle housing replacements.
New FlyerAug 30, 2017 - Lower riskMedical device
Carl Zeiss Meditec AG recalls Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena,
Carl Zeiss Meditec recalls specific INTRABEAM PRS 500 radiation therapy devices with incorrect calibration values on certificates. Affected units may not deliver accurate radiation doses.
Carl Zeiss MeditecAug 30, 2017 - Use cautionDrug
Noven Pharmaceuticals, Inc. recalls Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours (3.3 mg/hr) Rx Only Contains: 30 Patches
Noven Pharmaceuticals recalls Daytrana patches due to defective delivery systems that may not meet release liner or z-statistic specifications.
DaytranaAug 30, 2017 - Use cautionDrug
Pfizer Inc. recalls Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA.
Pfizer recalls Vancomycin Hydrochloride 750mg sterile powder for injection due to glass particles in vials. This poses a risk of serious injury during medical use. Affected products include specific lots from Hospira.
PfizerAug 30, 2017 - UnratedDrug
Mid Valley Pharmaceutical recalls Doctor Manzanilla Allergy & Decongestant Relief (diphenhydramine hydrochloride and phenylephrine hydrochloride) Syrup,
Mid Valley Pharmaceutical recalls Doctor Manzanilla Allergy & Decongestant Relief Syrup due to potential contamination with bacteria B. cepacia. Affected lots may pose health risks.
Mid Valley PharmaceuticalAug 30, 2017 - Lower riskFood
Lipari Foods, Inc. recalls Sunflower Seeds Honey Roasted, 12oz Tubs & 25lb Bulk
Lipari Foods recalls Honey Roasted Sunflower Seeds in 12oz tubs and 25lb bulk due to off taste from mislabeled shelf life. Consumers should check product codes and contact Lipari for details.
Lipari FoodsAug 30, 2017 - UnratedFood
ProSupps USA LLC recalls Dr. Jekyll Fruit Punch Domestic
Dr. Jekyll Fruit Punch Domestic contains unapproved ingredient picamilon. Consumers should stop using this product to avoid potential health risks.
Dr. JekyllAug 30, 2017 - Use cautionConsumer product
Dr. Brown's Natural Bottle & Dish Soaps Recalled by Handi-Craft Company Due to Risk of Bacteria Exposure
Dr. Brown's Natural bottle and dish soap recalled due to bacteria exposure risk. Immunocompromised individuals face infection risks. Stop using and contact for replacement.
Dr. Brown'sAug 30, 2017 - Use cautionVehicle
VOLVO VNL (2016) recall — Steering
Volvo is recalling certain 2016 VNL trucks with Dana Spicer steer axles that may have loose tie rods, risking loss of steering control. Owners should contact dealers for free inspections or replacements.
VolvoAug 29, 2017 - Lower riskMedical device
Becton Dickinson & Company recalls BD Vacutainer¿ K2 EDTA (K2E) 3.6mg Blood Collection Tube (13 x 75 mm x 2.0 mL). Catalog Number: 367841. Used for whole
Becton Dickinson recalls BD Vacutainer K2E blood collection tubes with catalog number 367841 due to potential inaccurate test results, which could delay treatment or cause serious health issues.
Becton DickinsonAug 29, 2017 - Lower riskDrug
Amerisource Health Services recalls Enalapril Maleate Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only. Packaged and Distributed by: American Health
Amerisource Health Services recalls 5 mg enalapril tablets due to failed stability specifications. This may affect medication safety. Check NDC 68084-390-01 for affected products.
Amerisource Health ServicesAug 29, 2017 - Lower riskDrug
Lucky Mart Inc. recalls PIYANPING Anti-Itch (hydrocortisone) Lotion, 1%, Net Wt. 0.67 oz (20g) tube, Manufactured By: Jimin Pharmaceutial Co.,
Lucky Mart recalls PIYANPING Anti-Itch Lotion (1% hydrocortisone) due to incorrect formulation containing dexamethasone. This may cause adverse reactions. Check NDC 68085-8012-4 and lots C16001/C16002.
Lucky MartAug 29, 2017
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,389 recalls tracked · 71,917 explained in plain English · 10,946 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.