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
CHEVROLET SILVERADO 3500 (2015) recall — Fuel System, Gasoline
Chevrolet is recalling 2015 Silverado 3500 trucks with a fuel system issue that could cause tank overfill, leading to potential fire risks. Owners should contact GM for free repairs.
ChevroletOct 19, 2017 - Use cautionVehicle
JEEP GRAND CHEROKEE (2017) recall — Engine And Engine Cooling
ATI recalls certain 2012-2017 Jeep Grand Cherokee SRT8 superchargers due to potential brake fluid leaks causing longer stopping distances. Owners must contact ATI for free replacement of supercharger brackets.
ATIOct 19, 2017 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2018) recall — Fuel System, Other
Daimler Trucks North America recalls 2012-2018 propane-powered Thomas Built Buses Saf-T-Liner C2 school buses due to potential propane leaks near transmission yoke that could cause fire if ignited.
Thomas Built BusesOct 19, 2017 - UnratedMedical device
Philips Electronics North America Corporation recalls CombiDiagnost R90 Image-Intensified fluoroscopic x-ray system CombiDiagnost R90 is a multi-functional general R/F
Philips recalls CombiDiagnost R90 X-ray systems where tube adapter-plate wiring was improperly installed, risking electrical hazards. Affected units may need repair or replacement.
PhilipsOct 19, 2017 - Use cautionMedical device
Cook Inc. recalls Mallinckrodt Institute Percutaneous Gastrostomy Set Product Usage: Intended for the percutaneous placement of a
Cook recalls Mallinckrodt Institute Percutaneous Gastrostomy Sets with backward-loaded wire guides. Affected lots include 6869315, 6908857, 7034661, 7106057, 7193431, 7252317, 7635697, 7744001, 7811587, 8025220, 8076495. Contact Cook for remedy.
CookOct 19, 2017 - UnratedMedical device
Ion Beam Applications S.A. recalls Proteus 235, Pencil Beam Scanning version PTS-6.4.11.X The Proton Therapy System - Proteus 235 (brand names: Proteus
Ion Beam Applications S.A. recalls Proteus 235 proton therapy systems due to potential range variability in radiation treatment planning. This may affect treatment accuracy for patients with localized tumors.
Ion Beam Applications S.A.Oct 19, 2017 - Use cautionMedical device
Datascope Corporation recalls BEQ-TOP 22702 ECC W/HMOD 30000, Catalog No. 701051179
Datascope recalls BEQ-TOP 22702 ECC W/HMOD 30000 (Catalog 701051179) due to potential air entry in ECMO circuits causing blood flow drops. Affected units have specific lot numbers.
DatascopeOct 19, 2017 - Lower riskMedical device
Johnson & Johnson Vision Care, Inc. recalls ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR
Johnson & Johnson Vision Care recalls ACUVUE ADVANCE contact lenses with HYDRACLEAR due to foreign matter complaints between blister and foil. Affected lots include B00DHLP (exp 08/2018) and L002FNL (exp 07/2020).
Johnson & Johnson Vision CareOct 19, 2017 - UnratedDrug
Allergan Sales, LLC recalls Combigan (brimonidine tartrate/timolol maleate ophthalmic solution) 0.2%/0.5%, Rx only, packaged in a) 2.5 mL NDC#
Allergan recalls Combigan eye drops (0.2%/0.5%) due to failed impurities and degradation specifications. Affected lots expire by Feb 2019. Consumers should contact Allergan for details.
AllerganOct 19, 2017 - UnratedDrug
SCA Pharmaceuticals, LLC recalls fentaNYL as citrate 2 mcg / mL, ROPIVacaine HCl 0.1%, Total Fentanyl Dose (200 mcg per 100 mL) in 0.9% Sodium Chloride
SCA Pharmaceuticals recalls fentanyl products with potential lack of sterility assurance. Affected items include specific doses in 0.9% sodium chloride solution. Consumers should contact the manufacturer for details.
SCA PharmaceuticalsOct 19, 2017 - Stop using nowFood
Market America Inc recalls bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc.,
Market America recalls 60-tablet bottles of Bliss Anti-Stress Formula due to undeclared Yohimbe, which can cause adverse reactions like dizziness and upset stomach.
Market AmericaOct 19, 2017 - Lower riskFood
Paragon Foods recalls Paragon Wholesale Foods, Warrendale, PA 15086 Label: Paragon; Best if used by 10/16/17; Broccoli Florets 1/2 Cup 50/1.7
Paragon Foods recalls broccoli florets potentially contaminated with Listeria monocytogenes. Consumers should check labels for best by dates and recall lots to avoid foodborne illness.
Paragon FoodsOct 19, 2017 - Lower riskFood
First Source, LLC recalls Apple Valley Honey Roasted Crunch, 15 lb. poly bag lined brown cardboard cases for bulk Item number: 5537606 UPC: 0
First Source recalls 15-lb honey roasted crunch bulk bags for undeclared almonds. Consumers should check item number 5537606 and lot code BD172621.
First SourceOct 19, 2017 - Lower riskFood
Giant Eagle, Inc. recalls Giant Eagle Breaded Shrimp Pittsburgh, PA 15238 PLU # 86815 refrigerated, packed in plastic clam shell. Sell by dates:
Giant Eagle voluntarily recalls Breaded Shrimp (PLU #86815) sold through Oct 19, 2017 due to undeclared egg allergen. Consumers should avoid products with lot codes up to best by Oct 24, 2017.
Giant EagleOct 19, 2017 - Use cautionFood
Albertsons Inc recalls Ready. Chef. Go! Halibut Fillet; UPC 231694 Items are made in store with generated scale label; sold as single,
Albertsons recalls Ready Chef Go Halibut Fillet products made with recalled vegetable ingredients that may contain Listeria monocytogenes. Consumers should check UPC 231694 and discard items with sell dates up to October 22, 2017.
AlbertsonsOct 19, 2017 - Stop using nowFood
Mann Packing Company, Inc. recalls Mann's Family Favorites Broccoli Cauliflower Florets, 16 oz bags - UPC 716519012174- US 12 oz bags - UPC 716519013034 -
Mann's Family Favorites Broccoli Cauliflower Florets bags with specific UPCs recalled due to Listeria monocytogenes detected in CFIA sampling. Consumers should check product labels for affected items.
MannOct 19, 2017 - Stop using nowConsumer product
Kids Preferred Recalls Wind-Up Musical Toys Due to Choking Hazard
Kids Preferred recalls wind-up musical plush toys with detachable metal parts that pose a choking hazard to young children. Consumers should stop using and return toys for free replacements.
Kids PreferredOct 19, 2017 - Lower riskMeat & poultry
Les Chateaux De France, Inc. Recalls Bacon-Wrapped Scallops due to Misbranding and an Undeclared Allergen
USDA FSIS recalls 4,225 pounds of bacon-wrapped scallops due to undeclared milk allergen and misbranding. Consumers urged not to consume; products should be thrown away or returned.
Les Chateaux De FranceOct 18, 2017 - Use cautionVehicle
TOYOTA SIENNA (2010) recall — Power Train
Toyota recalls 2010 Sienna vehicles where shift lever may move from Park without brake pedal depression, risking rolling. Owners must have shift lock solenoid replaced free by dealers.
ToyotaOct 18, 2017 - Use cautionVehicle
TOYOTA PRIUS (2016) recall — Hybrid Propulsion System
Toyota recalls certain 2016 Prius vehicles due to a capacitor not properly secured, which may shut down the hybrid system and increase crash risk. Owners will receive free inverter replacements by early December 2017.
ToyotaOct 18, 2017 - Use cautionVehicle
NISSAN ROGUE (2017) recall — Seats
Nissan recalls 2016-2017 Rogue vehicles with potentially unsafe seat welds that could increase crash injury risk. Owners must have seat frames inspected and replaced free of charge.
NissanOct 18, 2017 - Use cautionVehicle
VOLKSWAGEN TIGUAN (2018) recall — Exterior Lighting
Volkswagen is recalling 2018 Tiguan vehicles with dim back-up lights that could cause crashes. Owners must get free replacement taillight assemblies by December 15, 2017.
VolkswagenOct 18, 2017 - Use cautionMedical device
Teleflex Medical recalls Teleflex(R) Percuvance(TM) Percutaneous Surgical System, Components: (a) 5 mm Atraumatic Johans Grasper, Catalog Number
Teleflex recalls specific Percuvance surgical tools due to potential tool tip breakage during procedures, which could cause fragments to fall off. Affected items include 5mm Atraumatic Johans Grasper and other components with listed catalog numbers and lot numbers.
TeleflexOct 18, 2017 - Lower riskMedical device
BioMerieux SA recalls NucliSENS Lysis Buffer Extended lot for RES 76675
BioMerieux recalls specific lot of NucliSENS Lysis Buffer Extended for RES 76675 due to potential test inhibition from heme residue, risking inaccurate PCR results.
BioMerieuxOct 18, 2017 - Lower riskMedical device
Bioseal Corporation recalls Custom surgical kits labeled as follows: (a) Suture Removal Set, 910-0002 (b) Instrument Set, INST03/20 (c) Suture
Bioseal Corporation recalls custom surgical kits with expired Aplicare Providone Iodine Prep Pads. These kits may have incorrect expiration dates from Medline Industries' recall. Affected kits include specific models and lot numbers listed in the notice.
BiosealOct 18, 2017 - Lower riskFood
Myanmar Wholesale Trading recalls Thanlwin Fried Bean Snack, Net Weight 227 g 8 oz.. UPC 84682-00095 Product of Myanmar.
Myanmar Wholesale Trading recalls Thanlwin Fried Bean Snack (227g) due to undeclared peanuts. Consumers should check UPC 84682-00095 for affected products.
Myanmar Wholesale TradingOct 18, 2017 - Stop using nowMeat & poultry
Roundy's Supermarkets, Inc., Recalls Chili and Soup Products Due To Possible Foreign Matter Contamination
Roundy's Supermarkets recalls 16,320 pounds of chili and soup products from October 3, 2017, due to possible hard plastic contamination. Consumers are urged not to consume these items.
Roundy'sOct 17, 2017 - Use cautionMeat & poultry
GB Green Gastronome, LLC Recalls Chicken And Pork Products Due To Misbranding And Undeclared Allergens
USDA FSIS recalls 8,000 lbs of chicken/pork products with undeclared coconut milk and coconut cream (tree nut allergens) sold in Ohio/Pennsylvania. Consumers urged not to consume.
GB Green GastronomeOct 17, 2017 - Lower riskMedical device
Angiodynamics Inc. (Navilyst Medical Inc.) recalls Xcela PICC with PASV Valve Technology/Kit 5 F-55cm; (Maximum Flow Rate 3.5 mL/Sec)-indicated for short or long-term
Angiodynamics recalls Xcela PICC with PASV Valve Kit 5F-55cm due to mislabeling as 5F when it's actually 4F. This could lead to incorrect use in medical procedures.
AngiodynamicsOct 17, 2017 - Lower riskMedical device
Arrow International Inc recalls ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet
Arrow recalls PICC kits with possible 55cm catheter instead of 40cm. This mismatch may cause complications during medical procedures. Affected kits include CDC 34041 VPS Lot# 23F17A0037 and 23F17B0: 150 characters
ArrowOct 17, 2017
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83,390 recalls tracked · 71,917 explained in plain English · 10,946 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.