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
MERCEDES-BENZ SPRINTER 2500 (2015) recall — Power Train
Daimler Vans USA is recalling 2015 Mercedes-Benz Sprinter 2500 vehicles with a loose driveshaft that may puncture the fuel tank, risking fire. Owners must contact customer service for a free driveshaft catch strap installation.
Mercedes-BenzOct 2, 2017 - Use cautionVehicle
FREIGHTLINER SPRINTER 2500 (2016) recall — Air Bags
Daimler Vans USA is recalling 2016 Freightliner Sprinter 2500 vehicles with air bag control units that may not deploy properly after a crash, increasing injury risk. Owners must contact customer service for free repairs.
Daimler VansOct 2, 2017 - Use cautionVehicle
HEARTLAND ROAD WARRIOR (2017) recall — Equipment
Heartland is recalling 2017 Road Warrior toy haulers with faulty propane hoses that could leak gas near ignition sources, risking fire. Owners must have a flexible gas connector installed by dealers.
HeartlandOct 2, 2017 - Use cautionVehicle
AIRSTREAM FLYING CLOUD (2017) recall — Equipment
Airstream is recalling 2017 Flying Cloud trailers with missing spare tire placards that could lead to crashes if incorrect tires are used. Owners must get a corrected placard from dealers.
AirstreamOct 2, 2017 - Lower riskMedical device
Beckman Coulter Inc. recalls AQUIOS CL Flow Cytometer, Catalog No. B30166, Rx. The firm name on the label is Beckman Coulter Ireland Inc., Ireland.
Beckman Coulter recalls AQUIOS CL Flow Cytometers (Catalog B30166) due to potential sample misidentification when connected to laboratory systems. Affected units may require correction to prevent diagnostic errors.
Beckman CoulterOct 2, 2017 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls SOMATOM Go.Up computed tomography (CT) x-ray system table, Model Number: 11061628 Product Usage: Intended to generate
Siemens recalls SOMATOM Go.Up CT table model 11061628 with serial numbers 108054-108077 due to potential bolt loosening causing instability. Affected hospitals must address the issue to prevent table tipping.
SiemensOct 2, 2017 - UnratedMedical device
Edwards Lifesciences, LLC recalls Hemosphere System with the following three components: HEM1 Advanced Monitor, HEMSGM10 (Swan-Ganz Module), and
Edwards Lifesciences recalls Hemosphere System components due to software defects that may cause pre-procedural issues. Affected units include HEM1 Advanced Monitor, HEMSGM10 Swan-Ganz Module, and HEMOXSC100 Oximetry Smart Cable with specific serial numbers.
Edwards LifesciencesOct 2, 2017 - UnratedDrug
Unichem Pharmaceuticals Usa Inc recalls Bisoprolol Fumarate tablets, 5 mg, 30-count bottles, Rx only, Manufactured by: UNICHEM LABORATORIES, LTD. Pilerne Ind.
Unichem Pharmaceuticals recalls 5mg Bisoprolol Fumarate tablets due to potential impurity during stability testing. Affected lots manufactured in India, expiring 2017-2018. No specific remedy provided in recall notice.
UnichemOct 2, 2017 - Lower riskFood
Friendly Fruit Market dba Sid Wainer & Son recalls Sid Wainer & Son Jansal Valley brand Dried Chili De Arbol Peppers,packaged in a plastic clamshell container 1 ounce size
Sid Wainer & Son recalls 1-oz dried chili peppers with undeclared peanuts. Consumers should avoid these products to prevent allergic reactions.
Sid Wainer & SonOct 2, 2017 - UnratedFood
Allen's Blueberry Freezer, Inc. recalls Allen's Blueberries IQF Wild Blueberries, 30 lbs. corrugated box
Allen's Blueberries IQF Wild Blueberries (30 lbs) recalled due to Listeria monocytogenes contamination. Consumers should avoid use until notified.
Allen's BlueberryOct 2, 2017 - Use cautionVehicle
TESLA MODEL S (2012) recall — Air Bags
Tesla is recalling 2012 Model S vehicles due to potential air bag inflator rupture causing serious injury or death in crashes. Owners must have the front passenger air bag replaced free of charge.
TeslaOct 1, 2017 - Use cautionVehicle
SUBARU LEGACY (2012) recall — Air Bags
Subaru is recalling 2012 Legacy vehicles with air bag inflators that may rupture during crashes, causing serious injury or death. Owners must contact Subaru for free replacement.
SubaruOct 1, 2017 - Use cautionVehicle
NISSAN VERSA (2012) recall — Air Bags
Nissan recalls certain 2012 Versa hatchbacks with potential air bag inflator rupture causing serious injury or death. Owners must have inflators replaced free of charge by dealers.
NissanOct 1, 2017 - Stop using nowVehicle
LAND ROVER RANGE ROVER (2012) recall — Air Bags
Land Rover recalls certain 2012 Range Rovers due to air bag inflator rupture risk causing serious injury or death. Owners must replace front passenger air bag assemblies free of charge.
Land RoverOct 1, 2017 - Use cautionVehicle
JAGUAR XF (2012) recall — Air Bags
Jaguar is recalling 2012 XF vehicles with potentially dangerous air bag inflators that could rupture during crashes, causing serious injury or death. Owners must have the air bag assembly replaced free of charge.
JaguarOct 1, 2017 - Stop using nowVehicle
HONDA GL1800 (2012) recall — Air Bags
Honda is recalling 2012 GL1800 Goldwing motorcycles with air bag modules that may rupture during crashes, causing serious injury or death. Owners must contact Honda for free replacement.
HondaOct 1, 2017 - Use cautionVehicle
FORD FUSION (2012) recall — Air Bags
Ford is recalling 2012 Fusion vehicles with passenger air bag inflators that may rupture during crashes, causing serious injury or death. Owners must stop driving until repair is completed.
FordOct 1, 2017 - Stop using nowVehicle
ACURA TSX (2012) recall — Air Bags
Honda recalls certain 2012 Acura TSX models due to air bag inflator rupture risk causing serious injury or death. Owners must have the front passenger air bag replaced free of charge.
HondaOct 1, 2017 - Stop using nowVehicle
ACURA RL (2012) recall — Air Bags
Honda is recalling certain 2012 Acura RL vehicles due to a risk of air bag inflator rupture causing serious injury or death. Owners must have the front passenger air bag inflator replaced free of charge.
HondaOct 1, 2017 - Use cautionMedical device
Medtronic Navigation, Inc.-Littleton recalls O-arm¿ O2 interventional fluoroscopic x-ray system; Catalog Number: B1-700-02000 The O-arm O2 Imaging System is a
Medtronic recalls O-arm O2 imaging systems with specific serial numbers due to potential electrical shock during internal component servicing. Affected units may require repair to prevent shock to technicians.
MedtronicSep 30, 2017 - Lower riskMedical device
Ameditech Inc recalls Accutest Drug Test Cup 5+3 Product Usage: The Accutest Drug Test Cup is an in vitro diagnostic test for the rapid
Ameditech recalls Accutest Drug Test Cup 5+3 due to missing adulteration strip. This could lead to inaccurate test results. Affected units have part number DS84S625 and lot number 174886 (US distribution only).
AmeditechSep 30, 2017 - Use cautionMeat & poultry
Belmont Sausage Co. Recalls Smoked Turkey Drumstick Products Due To Misbranding and Undeclared Allergens
Belmont Sausage Co. recalls smoked turkey drumsticks due to undeclared milk allergen. Products contain milk not listed on labels and should be discarded or returned.
Belmont Sausage Co.Sep 29, 2017 - Use cautionVehicle
KIA SOUL (2016) recall — Steering
Kia recalls 2014-2016 Soul vehicles with potential pinion gear separation causing loss of steering. Owners must have steering gear inspected or replaced free by dealers.
KiaSep 29, 2017 - Use cautionVehicle
MITSUBISHI OUTLANDER (2017) recall — Electrical System
Mitsubishi recalls 2017 Outlander vehicles with defective relays that can cause engine stalls, leading to crash risks. Owners must contact MMNA for free relay replacement.
MitsubishiSep 29, 2017 - Use cautionVehicle
MASERATI QUATTROPORTE (2017) recall — Fuel System, Gasoline
Maserati recalls 2015-2017 Quattroporte GTS vehicles with V8 engines due to potential fuel pump failure causing engine stalls. Owners must contact for free replacement of fuel pump resistor cable assembly.
MaseratiSep 29, 2017 - Lower riskMedical device
Fresenius Medical Care Renal Therapies Group, LLC recalls NaturaLyte¿ Liquid Acid Concentrate 2.0 mEq/L, Model # 08-2251-0 3.43 liter bottle This concentrate is formulated to be
Fresenius Medical Care recalls NaturaLyte Liquid Acid Concentrate 2.0 mEq/L (Model 08-2251-0) due to potassium concentration exceeding 2.0 mEq/L in some batches, which may cause health risks during hemodialysis.
Fresenius Medical CareSep 29, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls BARD UROS AUTOMATED URINE OUPTUT AND TEMPERATURE MONITOR, MODEL BK10001M The Uros(TM) Automated Urine Output and
C.R. Bard recalls Uros Automated Urine Output and Temperature Monitor (BK10001M) due to potential inaccurate urine measurements affecting clinical decisions. Affected users should contact for details.
C.R. BardSep 29, 2017 - Lower riskMedical device
The Anspach Effort, Inc. recalls OSCILLATING SAW ATTACHMENT Surgical instrument motors and accessories/attachments are intended for use during surgical
Anspach Effort recalls surgical oscillating saw attachments shipped to non-veterinary customers due to a veterinary unit being mistakenly sent. This affects specific catalog and serial numbers.
Anspach EffortSep 29, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Vanguard Complete Knee System, Vanguard CR Lipped Tibial Bearing 10x71/75, Item Number: 183540 Product Usage: For use
Zimmer Biomet recalls Vanguard Complete Knee System with incorrect tibial bearing size labels. This may cause improper fit during surgery. Affected units sold between 2021-2022.
Zimmer BiometSep 29, 2017 - Lower riskMedical device
Abbott Laboratories, Inc recalls ARCHITECT c4000 part number 02P24; ARCHITECT c8000 part number 01G06; ARCHITECT c16000 part number 03L77 Clinical
Abbott recalls ARCHITECT c4000, c8000, and c16000 clinical chemistry systems due to potential tubing leaks from a manufacturing issue with the peristaltic head tubing connector.
AbbottSep 29, 2017
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