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- Lower riskMedical device
Alcon Research, Ltd. recalls ORA System with VerifEye+ Cart, Catalog Number 8065998307 For use during intraocular lens surgery
Alcon recalls specific ORA System VerifEye+ Carts for intraocular lens surgery due to potential incorrect IOL power measurements from a software error. Serial numbers listed in the notice.
AlconJun 30, 2017 - Use cautionMedical device
Sorin Group USA, Inc. recalls STOCKERT Heater-Cooler System 3T, 120V/60 Hz
Sorin Group recalls STOCKERT Heater-Cooler System 3T models with potential hydrogen peroxide diffusion risk. Affected units have specific serial numbers and item numbers. Contact for remedy details.
Sorin GroupJun 30, 2017 - Lower riskFood
Publix Supermarkets, Inc. (Deli Kitchen) recalls Publix Greenwise Cashew Butter, NET WT 16 oz (1 lb) 454g, Distributed by Publix Super Markets, Inc, Lakeland, FL 33802
Publix recalls 16 oz cashew butter jars that may accidentally contain almond butter. Consumers should check labels for the specific time code.
PublixJun 30, 2017 - Stop using nowVehicle
MAZDA CX-7 (2011) recall — Air Bags
Mazda recalls 2011 CX-7 vehicles with potentially dangerous air bag inflators that could rupture during crashes, causing serious injury or death. Owners must stop driving until repairs are completed.
MazdaJun 29, 2017 - Use cautionVehicle
HONDA CR-V (2011) recall — Air Bags
Honda is recalling 2011 CR-Vs with passenger air bags that may not deploy correctly in crashes, increasing injury risk. Owners should contact Honda for free repairs.
HondaJun 29, 2017 - Use cautionVehicle
CHEVROLET SILVERADO 1500 (2014) recall — Steering
General Motors recalls 2014 Chevrolet Silverado 1500 vehicles with potential temporary loss of electric power steering, increasing crash risk. Owners must update software at dealerships.
ChevroletJun 29, 2017 - Use cautionVehicle
TOYOTA TUNDRA (2016) recall — Air Bags
Toyota recalls 2016 Tundra vehicles with incorrect knee airbag mounting bolts that may loosen over time, increasing crash injury risk. Owners must contact Toyota for free repairs.
ToyotaJun 29, 2017 - Use cautionVehicle
HONDA ACCORD (2016) recall — Electrical System
Honda recalls 2016 Accord vehicles with electrical short risk due to water intrusion in battery sensor case. Owners can get free sensor replacement or adhesive fix from dealers.
HondaJun 29, 2017 - Use cautionVehicle
LEXUS ES350 (2017) recall — Steering
Toyota recalls 2017 Lexus ES350 vehicles with potential loose tie rod lock nut that could cause loss of steering and crash risk. Owners should contact Toyota for free repair.
ToyotaJun 29, 2017 - Use cautionVehicle
BUICK ENVISION (2017) recall — Structure
GM recalls 2016-2017 Buick Envisions with headliner assembly lacking energy-absorbing foam blocks, potentially increasing crash injury risk. Owners must contact GM for free replacement.
BuickJun 29, 2017 - Use cautionVehicle
NEWMAR KING AIRE (2018) recall — Fuel System, Diesel
Newmar is recalling 2018 King Aire motorhomes with Cummins ISX 15L engines due to a potential fuel pump failure causing engine stalls and crash risks. Owners must contact customer service for free fuel pump replacement.
NewmarJun 29, 2017 - Lower riskMedical device
Roche Diagnostics Corporation recalls Brand Name: ¿ cobas c 6000 MODULAR Series System e 601 ¿ cobas c 8000 MODULAR Series System - e 602 ¿ Roche / Hitachi
Roche recalls cobas c 6000 modular series (e 601) and cobas c 8000 modular series (e 602) systems due to a possible sample mismatch issue on the E170 module. The recall includes specific model numbers and serial numbers.
RocheJun 29, 2017 - UnratedMedical device
Zimmer Biomet, Inc. recalls PPS RingLoc+ Acetabular Shell, RNGLC+ LTD HOLE SHELL SZ62 The Porous Plasma Spray (PPS) Ringloc¿+ Acetabular System is
Zimmer Biomet recalls PPS RingLoc+ Acetabular Shell models with missing etching that could affect surgical fit. Affected units include model 11-116062, lot 374670. Consumers should contact the company for details.
Zimmer BiometJun 29, 2017 - Use cautionMedical device
Boston Scientific Corporation recalls SQ-RX 1010 Pulse Generator, Rx. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the
Boston Scientific recalls SQ-RX 1010 Pulse Generators due to potential memory corruption causing atypical energy delivery. Affected devices may deliver incorrect shock levels during life-threatening heart conditions.
Boston ScientificJun 29, 2017 - Use cautionMedical device
Medtronic Navigation, Inc. recalls Spine Referencing Instrumentation, Set, Contains Spinous Process Clamps, Short and Tall When used with a Medtronic
Medtronic recalls spine referencing clamps that may cause spinal injury if damaged during surgery. Learn if your clamps are affected and what to do.
MedtronicJun 29, 2017 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls ADVIA Alanine Aminotransferase (ALT) reagent chemistry assays; ALT intended to measure the activity of the enzyme
Siemens Healthcare recalls ALT reagent assays that may cause false high or low drug results for sulfasalazine and sulfapyridine. Affected products include specific part numbers sold by Randox Laboratories.
Siemens HealthcareJun 29, 2017 - Lower riskMedical device
Medtronic Navigation, Inc. recalls Medtronic ENT Prgm 9734636 Add Fusion Nav AxiEM, reusable, Rx. This kit includes 9733908 (which includes 9733452
Medtronic recalls ENT suction kits that fail instrument verification. These reusable surgical tools may not pass pre-use checks, risking improper function during procedures.
MedtronicJun 29, 2017 - Lower riskMedical device
Sorin Group USA, Inc. recalls SORIN GROUP, SMART PERFUSION PACK, SMART 1/4" PEDS PACK, REF 627262502, STERILE EO, Rx Only, 1 EA
Sorin Group recalls SMART Perfusion Packs with potential sterile barrier breaches due to small pinholes in packaging. Affected units include specific lot numbers.
Sorin GroupJun 29, 2017 - UnratedDrug
Teva Pharmaceuticals USA recalls Buprenorphine and Naloxone Sublingual Tablets, 2 mg/0.5 mg 30 tablets per bottle, Rx only, Distributed by: Teva
Teva Pharmaceuticals USA recalls specific lots of Buprenorphine and Naloxone sublingual tablets (2mg/0.5mg) due to failed impurities tests. These prescription-only products may contain unsafe levels of related compounds.
TevaJun 29, 2017 - Use cautionConsumer product
Design Solutions International with Home Depot Recalls Light Fixtures Due to Laceration and Burn Hazards
Design Solutions International recalls Home Decorators Collection 3-Light and 4-Light Comotti Vanity Fixtures due to risk of laceration and burn from detached glass shades.
Design Solutions InternationalJun 29, 2017 - Stop using nowConsumer product
Burt's Bees Baby Recalls Infant Coveralls Due to Choking Hazard
Burt's Bees Baby recalls infant Butterfly Garden Coveralls with style LY24195 due to a choking hazard from a detachable snap at the crotch. Affected items were sold from August 2016 with specific sizes and colors.
Burt's Bees BabyJun 29, 2017 - Lower riskMeat & poultry
Vinh Hoan USA, Inc. Recalls Siluriformes Fish Products Due To Failure To Comply With FSIS Import Requirements
USDA FSIS recalls 84,000 lbs of frozen Swai fillets imported from Vietnam without USDA inspection. Consumers are urged not to eat these products and should discard or return them.
Vinh HoanJun 28, 2017 - Use cautionVehicle
LANCE TRAVEL TRAILER (2018) recall — Equipment
Lance Camper is recalling 2018 Travel Trailers with unsecured bicycle racks that could contact the road, increasing crash risk. Owners get refunds or free front bike racks.
Lance CamperJun 28, 2017 - Lower riskMedical device
GE Inspection Technologies, LP recalls GE Inspection Technologies Blade|line Industrial Cabinet X-ray system
GE Inspection Technologies recalls certain Blade|line Industrial Cabinet X-ray systems due to potential excess radiation emissions under the cabinet, which may exceed safety limits. Affected units have specific serial numbers and were sold between 2013-2014.
GE Inspection TechnologiesJun 28, 2017 - Lower riskDrug
Valeant Pharmaceuticals North America LLC recalls Obagi-C Rx System C-Therapy Night Cream, Net wt. 2 oz. (57g) bottle, Rx only, Distributed by OMP, Inc., Long Beach, CA
Obagi-C Rx System C-Therapy Night Cream (2 oz) is recalled due to missing product instructions. Consumers should check labels for NDC 62032-222-02 and lot 2578400. This affects prescription-only products sold in the US.
ObagiJun 28, 2017 - Lower riskDrug
GSK Consumer Healthcare recalls parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and Antigingivitis Toothpaste, 0.454% (0.15% w/v
GSK Consumer Healthcare recalls Parodontax Whitening toothpaste due to potential metal contamination. Affected products contain 0.454% stannous fluoride and may pose a foreign substance risk. Consumers should check product details and follow official instructions.
GSK Consumer HealthcareJun 28, 2017 - Lower riskFood
Kettle Foods, Inc. recalls Kettle Brand Krinkle Cut Potato Chips Spicy Queso, 8.5 oz., Distributed by: Kettle Foods, Inc., Salem, OR 97301, UPC:
Kettle Foods recalls Spicy Queso Potato Chips due to inaccurate carbohydrate labeling on nutrition facts. The product lists 3g per serving but contains 15g. Consumers should check for specific dates and UPC codes.
KettleJun 28, 2017 - Lower riskFood
Taylor Farms Texas, Inc. recalls Starbucks PB & J Fruit and Veggies 7.4 oz. (210 g) UPC: 7 62111 23607 4
Taylor Farms recalls Starbucks PB & J Fruit and Veggies 7.4 oz. due to soy lecithin not being listed on the label. Consumers should check the UPC 7 62111 23607 4 for affected products.
Taylor FarmsJun 28, 2017 - Lower riskFood
Dierbergs Markets, Inc Corporate Office recalls Dierbergs Kitchen, Grilled Chicken Caesar Wrap, NET WT. 10 oz, UPC 0 233983 804994
Dierbergs recalls 10oz Grilled Chicken Caesar Wraps (7/2/17 and earlier) due to undeclared anchovy. Consumers should check UPC 0233983804994 for affected items.
DierbergsJun 28, 2017 - Stop using nowConsumer product
South Shore Expands Recall of Chest of Drawers Due to Serious Tip-Over and Entrapment Hazards
South Shore recalls 5-drawer chests with unstable design that can tip over or entrap children, risking serious injury or death. Consumers must anchor to wall or get free restraint kit.
South ShoreJun 28, 2017
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