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- UnratedDrug
Simple Diagnostics, Inc. recalls Alcohol Prep Pads (Isopropyl Alcohol USP 70% v/v), 100 Individual Pads, Sterile, Distributed by Simple Diagnostics,
Simple Diagnostics recalls 100-count alcohol prep pads (70% isopropyl alcohol) that may not be sterile, posing infection risks. Affected lots expire 09/2019 or 12/2019.
Simple DiagnosticsSep 5, 2017 - UnratedDrug
Genentech, Inc. recalls Activase (alteplase), 100 mg (58 million IU), Lyophilized vial, packaged with 1 single-dose 100ml vial of sterile water
Genentech recalls 58 million IU Activase vials due to cracked glass in sterile water vials, posing contamination risks. Consumers should check for cracks and contact Genentech for details.
GenentechSep 5, 2017 - Lower riskDrug
Teva Pharmaceuticals USA recalls Acarbose Tablets, 25 mg, 100-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia BBG3000,
Teva Pharmaceuticals USA recalls Acarbose Tablets 25mg 100-count bottles due to incorrect expiration date (July 2018) printed on labels instead of July 2017. This may lead to medication safety issues.
Teva Pharmaceuticals USASep 5, 2017 - Stop using nowDrug
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company recalls Sterile Eyewash (sterile isotonic phosphate buffered saline solution), 4 oz. 24 units per box. Manufactured by Medex
Smiths Medical recalls 4 oz sterile eyewash bottles due to leaking containers that lack sterility assurance, posing an infection risk.
Smiths MedicalSep 5, 2017 - Use cautionDrug
Aidarex Pharmaceuticals LLC recalls Phentermine, USP Capsules, 15 mg, 30 count bottles, Rx only, Packaged By: Aidarex Pharmaceuticals, Corona, CA, MFG:
Aidarex Pharmaceuticals recalls specific lots of 15mg Phentermine capsules due to failed impurity specifications. Check your bottle's batch number and expiration date.
Aidarex PharmaceuticalsSep 5, 2017 - Lower riskFood
NOW Foods recalls Organic Coconut Sugar, 16oz bag, 12 bags/case, packed in a foil bag
Now Foods recalls 16oz organic coconut sugar bags labeled gluten-free due to undeclared gluten. Affected lots from Dec 2016 to June 2017. Consumers should check batch numbers and contact company for details.
Now FoodsSep 5, 2017 - Lower riskFood
Wegmans Food Markets, Inc. recalls Wegmans Assorted Muffins 4-Pack-18 oz. (1 lb. 2 oz.) 510g packaged in clear plastic shell. UPC: 77890-22744 .
Wegmans recalls 4-pack muffins due to walnuts not listed on ingredient labels, posing allergy risk. Check UPC 77890-22744 for affected products.
WegmansSep 5, 2017 - Stop using nowConsumer product
ASHERANGEL Recalls Children's Sleepwear Due to Violation of Federal Flammability Standard; Sold Exclusively at Amazon.com (Recall Alert)
ASHERANGEL recalls children's nightgowns and pajama sets that fail federal flammability standards, risking burn injuries. Consumers must stop using and return for full refunds.
ASHERANGELSep 5, 2017 - Stop using nowConsumer product
American Honda Recalls Motocross Off-Road Motorcycles Due to Crash and Injury Hazards (Recall Alert)
Honda recalls 2015-2016 CRF450R motocross bikes due to transmission gear failure causing crashes. Owners must stop using and get free repairs from authorized dealers.
HondaSep 5, 2017 - Use cautionVehicle
GILLIG LOW FLOOR (2016) recall — Visibility/Wiper
Gillig recalls certain 2016-2017 Low Floor transit buses with wiper arms that can crack, causing reduced visibility and crash risk. Owners will receive free wiper arm replacements.
GilligSep 3, 2017 - Use cautionVehicle
JAGUAR F-PACE (2017) recall — Power Train
Jaguar recalls 2017 F-Pace vehicles with potential driveshaft detachment causing loss of drive power and crash risk. Owners must have driveshafts inspected and replaced free of charge by dealers.
JaguarSep 3, 2017 - Use cautionVehicle
AIRSTREAM BASECAMP (2017) recall — Suspension
Airstream recalls 2017 Base Camp trailers due to tire failure risk when heavily loaded, causing potential crashes. Owners must contact customer service for free axle replacement.
AirstreamSep 3, 2017 - Use cautionVehicle
MAZDA MAZDA3 (2011) recall — Seats
Mazda recalls 2011 Mazda3s with manual seat lifters that may break, causing driver to lose proper driving position and increasing crash risk. Owners must have seat inspected or replaced free.
MazdaSep 2, 2017 - Use cautionVehicle
SUZUKI GRAND VITARA (2013) recall — Power Train
Suzuki recalls 2009-2013 Grand Vitara vehicles with manual transmission due to risk of gear shift failure causing crashes. Owners must contact Suzuki for free repair.
SuzukiSep 2, 2017 - Use cautionVehicle
JAGUAR XF (2017) recall — Fuel System, Gasoline
Jaguar is recalling 2017 XF vehicles with a cracked left inner sill panel that could rupture fuel lines during a crash, risking fire. Owners must contact Jaguar for free repurchase or replacement.
JaguarSep 2, 2017 - Use cautionVehicle
BMW I3 (2017) recall — Fuel System, Gasoline
BMW is recalling certain 2014-2017 i3 REx hybrid electric vehicles due to a fuel vapor leak risk that could cause fire if an ignition source is present. Owners should contact BMW for free repairs.
BMWSep 2, 2017 - Lower riskFood
Country Fresh Products, LLC recalls Tri-Pepper Dice, 6-oz. packaged in a clamshell and Dice Tri-Pepper, 7-oz. packaged in a clamshell
Country Fresh recalls Tri-Pepper Dice products due to potential Listeria monocytogenes contamination. Products with use by dates 8/12-19/2017 and 8/13-20/2017 are affected.
Country FreshSep 2, 2017 - Use cautionVehicle
MCLAREN MP4-12C SPIDER (2012) recall — Air Bags
McLaren is recalling 2012 MP4-12C Spider vehicles with faulty air bag inflators that may rupture during crashes, causing serious injury or death. Owners must have inflators replaced free by November 13, 2017.
McLarenSep 1, 2017 - Use cautionVehicle
LEXUS ES350 (2012) recall — Air Bags
Toyota is recalling 2012 Lexus ES350 vehicles with potential air bag inflator rupture causing serious injury or death. Owners must contact Toyota or Pontiac for free air bag replacement.
ToyotaSep 1, 2017 - Use cautionVehicle
HEARTLAND MALLARD (2017) recall — Equipment
Heartland is recalling 2017 Mallard trailers with potentially incorrect tire size/pressure labels that could cause crashes. Owners must get a corrected label from dealers.
HeartlandSep 1, 2017 - Use cautionMedical device
Baxter Healthcare Corp recalls Baxter Amia Automated Peritoneal Dialysis Set with Cassette, REF 5C5479
Baxter recalls Amia Automated Peritoneal Dialysis Sets with Cassette (lot numbers listed) due to missing red line and flow alerts. Affected users should check their lot numbers.
BaxterSep 1, 2017 - Lower riskMedical device
Elekta Inc recalls Elekta ERGO++ Product Usage: ERGO is often used for stereotactic treatments.
Elekta recalls ERGO++ software version 1.7.3+ for stereotactic treatments due to incorrect DICOM mapping of collimator/couch angles, potentially causing inaccurate radiation therapy planning.
Elek:taSep 1, 2017 - Lower riskMedical device
Aaren Scientific Inc. recalls AERO IOL Injection System containing 10 Z28 Cartridges per box, Part #003500-0025-282, Sterile, Rx. The firm name on
Aaren Scientific recalls AERO IOL Injection System with incorrect storage temperature label. This may affect product sterility if stored improperly. Contact for details.
Aaren ScientificSep 1, 2017 - Use cautionMedical device
Respire Medical recalls Respire Pink Series EF+ Oral Sleep Apnea Device.
Respire Medical recalls one Respire Pink Series EF+ oral sleep apnea device (Serial No. 50837) due to potential breakage during use.
Respire MedicalSep 1, 2017 - Use cautionMedical device
Permobil, Ab recalls Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500
Permobil recalls electric wheelchair bases C300, C350, C400, and C500 with potential top plate assembly failure. Affected units have specific serial numbers listed in the recall notice.
PermobilSep 1, 2017 - UnratedMedical device
Aesculap Implant Systems LLC recalls The ELAN 4 Air System is intended for high speed cutting, sawing and drilling of bone in fields of Spine, ENT, Neuro,
Aesculap recalls ELAN 4 Air System devices for spine, ENT, neuro and maxillofacial surgery that were sold without FDA clearance. This unapproved device may pose risks during surgical procedures.
AesculapSep 1, 2017 - Lower riskMedical device
CooperVision Inc. recalls Biofinity XR Toric contact lenses 8.7/14.5 - 6PK Biofinity XR Toric (comfilcon A) Soft (Hydrophilic) Contact Lenses are
CooperVision recalls Biofinity XR Toric contact lenses with incorrect labeling on Made-To-Order blister packs. The label shows 'Biofinity Multifocal Toric' instead of 'Biofinity XR Toric'. This may cause confusion in prescription use. Affected lots and expiration dates listed.
CooperVisionSep 1, 2017 - Lower riskDrug
Pharmedium Services, LLC recalls Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection USP in 1000 mL bag Rx Only, Compounded by PharMEDium
PharMEDium Services recalls oxytocin compounded in lactated Ringer's injection due to subpotent drug risk. Affected units may not deliver proper medication strength.
PharMEDiumSep 1, 2017 - Stop using nowDrug
Pfizer Inc. recalls Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL
Pfizer recalls sterile water vials with potential cracked glass that could cause contamination. Affected vials were manufactured by Hospira in Lake Forest, IL. Stop using if you have these vials.
PfizerSep 1, 2017 - Use cautionVehicle
THOR MOTOR COACH SERRANO (2011) recall — Electrical System
Thor is recalling 2011 Serrano motorhomes with a faulty transfer switch that may overheat and cause fire. Owners must contact TMC for free replacement.
ThorAug 31, 2017
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