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
FREIGHTLINER SPRINTER 2500 (2011) recall — Air Bags
Daimler Vans USA recalls 2010-2011 Freightliner Sprinter 2500 vehicles with faulty air bags that may rupture during crashes, causing serious injury or death. Owners must have the front passenger air bag replaced free by dealers.
Daimler Vans USAJul 28, 2017 - Stop using nowVehicle
FREIGHTLINER SPRINTER 2500 (2012) recall — Air Bags
Daimler Vans USA recalls 2012 Freightliner Sprinter 2500/3500 vehicles with faulty air bags that may rupture during crashes, causing serious injury or death. Owners must have front passenger air bags replaced free by dealers.
Daimler Vans USAJul 28, 2017 - Use cautionVehicle
CHRYSLER PACIFICA (2017) recall — Power Train
Vantage Mobility is recalling certain 2017 Chrysler Pacifica vehicles with potential wheel wobble causing loss of control. Owners must contact VMI for free pinion bracket replacement.
Vantage MobilityJul 28, 2017 - Use cautionVehicle
BMW R1200 GS (2018) recall — Equipment
BMW recalls 2014-2018 R1200GS and R1200GS Adventure motorcycles with optional aluminum luggage cases that may block rear reflectors, increasing crash risk. Owners must contact BMW for free reflector installation.
BMWJul 28, 2017 - Lower riskMedical device
Cardinal Health 200, LLC recalls Convertors Robotic Drape with Attached Leggings; Product is packaged as Single Sterile Drape/8 per Case
Cardinal Health recalls robotic drapes with incorrect packaging labels that may cause confusion during medical procedures. Affected units include Lot 17DAH349.
Cardinal HealthJul 28, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female, 14 FR (30/box), Rx Only intended for urinary
C.R. Bard recalls specific lots of Magic 3 Antibacterial Hydrophilic Intermittent Catheters that may lack the hydrophilic coating, increasing infection risk. Affected units have catalog numbers 51514 and lots 53623024, 53623054, 53623047, 53623122.
C.R. BardJul 28, 2017 - Stop using nowMedical device
NXTHERA recalls Rezum System, Vapor BPH Ablation System, Model Number D2201-003. NxThera Inc. 7351 Kirkwood Lane Suite 138 Maple Grove,
NxThera recalls Rezum System (Model D2201-003) due to potential needle bond failure during prostate treatment. This may cause injury during BPH ablation procedures for men over 50 with specific prostate sizes.
NxTheraJul 28, 2017 - Lower riskMedical device
Roche Diagnostics Corporation recalls Cobas 8000 Modular Series system; Software Version 05-02 and 06-03; UDI: 05641446001
Roche recalls Cobas 8000 Modular Series systems with specific software versions due to potential incorrect test results. Affected units have unique serial numbers listed in the recall notice.
RocheJul 28, 2017 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc recalls ADVIA Centaur¿ T3 ADVIA Centaur T3: For in vitro diagnostic use in the quantitative determination of triiodothyronine
Siemens Healthcare recalls ADVIA Centaur T3 diagnostic kits with specific lot numbers due to potential barcode scanning errors affecting thyroid disease testing accuracy.
Siemens HealthcareJul 28, 2017 - Use cautionMedical device
Brainlab AG recalls AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO is intended to be used for X-ray computed
Brainlab recalls AIRO Mobile CT System (MobiCT-32) due to risk of unintended motion in transport mode. All units released since April 2014 with specific serial numbers are affected.
BrainlabJul 28, 2017 - Lower riskDrug
PD-Rx Pharmaceuticals, Inc. recalls Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC
PD-Rx Pharmaceuticals recalls Famotidine 20mg tablets due to weight specification failure. Affected lots may have incorrect tablet weight.
PD-Rx PharmaceuticalsJul 28, 2017 - Lower riskFood
SIlver HIlls Bakery recalls Aldi liveGfree Gluten Free Classic Soft White Hamburger Buns, 11.3 Ounces, in plastic bag
Aldi's gluten-free hamburger buns with undeclared eggs are being recalled. Consumers should check packaging for lot numbers ending in 0897 to avoid potential allergic reactions.
Silver Hills BakeryJul 28, 2017 - Stop using nowConsumer product
Nestlé Waters North America Recalls AccuPure Water Dispensers Due to Fire and Burn Hazards (Recall Alert)
Nestlé Waters recalls AccuPure floor-standing water dispensers with model HB215-3G (black) and HW215-3G (white) due to fire and burn risks from overheating. Consumers must stop using immediately and contact Nestlé Waters for replacement.
NestlăJul 28, 2017 - Use cautionVehicle
INFINITI Q50 (2018) recall — Fuel System, Gasoline
Nissan is recalling 2016-2018 Infiniti Q50 vehicles with faulty fuel pump software that may cause engine stalling while driving. Owners must contact Infiniti for free software update.
InfinitiJul 27, 2017 - Use cautionVehicle
FLEETWOOD PACE ARROW (2018) recall — Exterior Lighting
REV is recalling 2018 Fleetwood Pace Arrow motorhomes with non-tempered headlight lenses that may crack, causing reduced lighting and crash risk. Owners should contact REV customer service for free lens replacement.
REVJul 27, 2017 - Lower riskMedical device
Medtronic Navigation, Inc. recalls VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559 Visualase Cooled Laser Applicator System 3mm Tip;
Medtronic recalls VCLAS 3mm, 10mm, and 15mm laser tips due to potential saline leakage during manufacturing. Affected units include specific part numbers and lots. Consumers should contact Medtronic for details.
MedtronicJul 27, 2017 - Lower riskMedical device
Zimmer Surgical Inc recalls A.T.S. 2200TS Tourniquet Systems, Personalized Pressure. Zimmer Surgical, Inc. Dover, OH 44622 Intended to be used by
Zimmer Surgical recalls A.T.S. 2200TS Tourniquet Systems with updated labels and reduced RF communication distance requirements. Affected units have specific serial numbers and lot numbers listed in the recall notice.
Zimmer SurgicalJul 27, 2017 - Lower riskMedical device
Baxter Healthcare Corporation recalls Empty IntraVia Container with Non-DEHP Fluid Path, 500mL Containers are intended for use in the preparation and
Baxter Healthcare recalls empty 50:00mL IntraVia containers with non-DEHP fluid paths due to potential microbial contamination from leaks. Affected units have product code 2J8003 and lot number DR16J18096.
Baxter HealthcareJul 27, 2017 - Use cautionMedical device
Datascope Corporation recalls Maquet Cardiopulmonary Bypass Custom Tubing kit BO-TOP 38600 ADULT CPB, Part Number 701056035 Product Usage: The Maquet
Maquet recalls adult cardiopulmonary bypass tubing kits with potential flow blockage risk. Affected units have part number 701056035. Consumers should contact for details.
MaquetJul 27, 2017 - UnratedMedical device
Optovue, Inc. recalls iFusion, Device Listing Number D203271. Product Usage: The iCam is a non-contact, high resolution digital imaging
Optovue recalls iFusion eye imaging devices due to missing FDA approval for Vault Mapping software. The recall affects specific model numbers sold for retinal imaging. Consumers should contact Optovue for details.
OptovueJul 27, 2017 - Lower riskFood
Newark Nut Stores, Inc. recalls Bourbon Street Mix, 157 25 lbs cases and 2,509 one (1) lb bags.
Newark Nut Stores recalls Bourbon Street Mix bags due to undeclared cashews. Consumers should check product labels for the recall.
Newark Nut StoresJul 27, 2017 - Stop using nowConsumer product
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Really Good Stuff Recalls Magnetic Dry Erase Boards Due to Laceration Hazard (Recall Alert)
Really Good Stuff recalls Write Again magnetic dry erase boards because the metal surface can separate, causing cuts. Stop using and contact for a replacement.
Really Good StuffJul 27, 2017 - Lower riskMedical device
Molnlycke Health Care, Inc recalls 9x15" Medium Utility Positioner with Cover
Molnlyke Health Care recalls 9x15" Medium Utility Positioner with Cover due to possible metal shavings. Affected units may not meet specifications. Contact for remedy details.
Molnly:keJul 26, 2017 - Lower riskMedical device
Synthes (USA) Products LLC recalls 2.5 mm Reaming Rod, Ball tip, 950 mm, sterile, Part Number: 351.706S Reaming Rods are intended for guiding of reamers
Synthes recalls 2.5mm reaming rods with potential sterility issues due to packaging seal gaps. These surgical tools were distributed from March 21 to June 23, 2017. Check product lot numbers for affected items.
SynthesJul 26, 2017 - Use cautionMedical device
DePuy Orthopaedics, Inc. recalls Concorde Lift Torque Limiting Handle. Must be used with supplemental internal spinal fixation systems that have been
DePuy Orthopaedics recalls Concorde Lift Torque Limiting Handles used in spinal surgery. Potential for intra-operative breakage of driver tips could cause complications during spinal procedures.
DePuy OrthopaedicsJul 26, 2017 - Stop using nowDrug
ICU Medical Inc recalls 0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA
ICU Medical recalls 1000mL 0.9% Sodium Chloride Injection due to possible stainless steel particles. Affected units have NDC# 0409-7983-09 and lot 61-841-FW expiring 01/01/2018.
ICU MedicalJul 26, 2017 - Stop using nowDrug
HOSPIRA INC, LAKE FOREST recalls Hydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial. Mfd For: Teva Parenteral
Hospra recalls 50 mL Hydromorphone injection vials due to silicone oil particles. This may cause serious injury if injected. Check NDC 0703-0018-01 and lot 560053F.
HospraJul 26, 2017 - Stop using nowFood
NatureAll-STF Holding, LLC recalls Heart-Plus, No. 83, 120 Capsules, Dietary Supplement
NatureAll recalls Heart-Plus dietary supplements due to undeclared soy. Check your bottle lot numbers for details on this Class II recall.
NatureAllJul 26, 2017 - Use cautionMeat & poultry
D & D Foods, Inc. Recalls Pizza Products Due To Misbranding and Undeclared Allergens
USDA recalls 17,847 pounds of Hy-Vee pepperoni pizzas with undeclared soy lecithin allergen. Consumers urged to stop using these products immediately.
D & D FoodsJul 25, 2017 - Stop using nowVehicle
FORD ESCAPE (2015) recall — Seat Belts
Ford recalls certain 2015 Escapes due to seat belt anchor bolts that may fracture, increasing injury risk in a crash. Free repair available.
FordJul 25, 2017
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