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
34,896 found- Stop using nowConsumer product
American Honda Recalls Recreational Off-Highway Vehicles Due to Fire and Burn Hazard (Recall Alert)
Honda recalls 2016-2018 Pioneer 1000 ROVs due to muffler overheating that can melt plastic heat shields and cause fires. Affected vehicles sold in red, blue, green, gray, and yellow.
HondaMay 15, 2018 - Use cautionVehicle
BMW 335D (2011) recall — Electrical System
BMW recalls 2010-2011 335d diesel vehicles with electrical system issues that may cause unexpected stalling and crash risk. Owners must have the connector replaced free by dealers.
BMWMay 14, 2018 - Use cautionVehicle
KEYSTONE MONTANA (2018) recall — Electrical System
Keystone is recalling 2018 Montana fifth-wheel trailers due to a fire risk from slide-out switch wiring lacking circuit protection. Owners must contact customer service for free fuse installation.
KeystoneMay 14, 2018 - Use cautionVehicle
FORD ECOSPORT (2018) recall — Equipment
Ford is recalling 2018 Ecosport vehicles with European-style brake fluid caps that could lead to incorrect brake fluid replacement, risking brake failure and crashes. Owners will receive free cap and manual replacements.
FordMay 14, 2018 - Lower riskMedical device
Merck Millipore Ltd. recalls Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon
Merck Millipore recalls Minicon B-15 and CS-15 clinical sample concentrators used over 6 months after manufacture due to potential delays in diagnostic test results. Affected units have specific lot numbers.
Merck MilliporeMay 14, 2018 - UnratedMedical device
CryoLife, Inc. recalls Cryovalve(R) SG Pulmonary Human Heart Valve, Catalog Number SGPVVOO
CryoLife recalls Cryovalve SG Pulmonary Heart Valve (Catalog SGPVVOO) after autopsy reports found morphine in patient urine. This may indicate improper use or contamination.
CryoLifeMay 14, 2018 - Lower riskMedical device
O-Two Medical Technologies, Inc. recalls O-Two Equinox¿ Relieve N2O/O2 Analgesic Gas Mixing and Delivery System Model#: 01EQ1000
O-Two Medical recalls Equinox Relieve N2O/O2 mixing system model 01EQ1000 due to potential higher nitrous oxide delivery than specified. Affected units have serial numbers EQ1332-17 to EQ3003-18.
O-TwoMay 14, 2018 - Stop using nowMedical device
Maquet Cardiopulmonary Ag recalls Aortic Arterial Cannula 22 Fr (O.D.); 23 cm (L); with 3/8-inch connector with LL, Part Number 701002246, Article Number
Maquet recalls aortic arterial cannulas with potential 3/8-inch de-airing plugs that could break during removal, causing injury during cardiopulmonary bypass procedures.
MaquetMay 14, 2018 - Lower riskMedical device
Opgen Inc recalls AdvanDx QuickFISH Slides, a component of the QuickFish BC Fixation Kit - BC, REF QFFIXBC1-25, Catalog Number: CS012
Opgen recalls AdvanDx QuickFISH Slides (lot 17306401) that may not perform correctly after their November 2018 expiration date. Consumers should check if their slides expire before November 2018.
OpgenMay 14, 2018 - UnratedMedical device
Encore Medical, Lp recalls Foundation Modular Femoral Stem, Part Number, 220-10-110. Knee prosthesis component. The Foundation Revision Knee is a
Encore Medical recalls Foundation Revision Knee prosthesis component (part 220-10-110) due to lack of FDA clearance. This unapproved device may pose risks for patients needing knee replacements.
Encore MedicalMay 14, 2018 - Use cautionMedical device
Beaver Visitec recalls Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery
Beaver Visitec recalls Safety Sideport Knife 1.0mm 45° (Lot 6002436 & 6002663) due to loose blades that may fall out during ophthalmic surgery. Affected users should contact for remedy.
Beaver VisitecMay 14, 2018 - Lower riskFood
Michael's Bakery Products, LLC recalls Gluten Free Chunky Chocolate Product, 20051, Size: 2.0 oz, Case Pack: 168, Net Wt: 21 LBS, UPC 1009606720051
Michael's Bakery recalls gluten-free chocolate product for missing pecan ingredient labeling on packaging. Consumers should check for lot number 17356.
Michael's BakeryMay 14, 2018 - Stop using nowConsumer product
Harbor Freight Tools Recalls Chainsaws Due to Serious Injury Hazard
Harbor Freight recalls 14-inch electric chainsaws with faulty power switch that may continue running after being turned off, posing serious injury risk. Return for free replacement by May 21, 2018.
Harbor Freight ToolsMay 14, 2018 - Use cautionVehicle
AUDI A6 (2016) recall — Electrical System
Volkswagen recalls 2016 Audi A6 sedans with faulty auxiliary heater connector that may overheat and cause fire. Owners must have connector inspected and replaced free by dealers.
AudiMay 12, 2018 - Use cautionVehicle
VOLKSWAGEN GOLF R (2018) recall — Fuel System, Gasoline
Volkswagen recalls 2018 Golf R vehicles with a fuel hose that may detach, causing leaks and fire risk. Owners must contact customer service for free repairs.
VolkswagenMay 12, 2018 - Use cautionVehicle
THOR MOTOR COACH VENETIAN (2019) recall — Service Brakes, Air
Thor Motor Coach is recalling 2018-2019 Venetian motorhomes due to loose brake caliper bolts that could reduce brake effectiveness and increase crash risk. Owners should contact TMC for free brake checks.
Thor Motor CoachMay 11, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Vanguard Knee System PS Tibial Bearing, Part Number 183621 Intended for use in knee joint replacement procedures.
Zimmer Biomet recalls Vanguard Knee System PS Tibial Bearing (Part 183621) due to incorrect size labeling in the label master file, which could lead to improper knee joint replacement procedures.
Zimmer BiometMay 11, 2018 - Lower riskMedical device
Arrow International Inc recalls Multi-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter, CS-15853-E Product CVCs are intended to
Arrow recalls Multi-Lumen Central Venous Catheterization Sets with Blue FlexTip Catheter (CS-15853-E) due to potential increased resistance during insertion, which may require medical intervention.
ArrowMay 11, 2018 - Lower riskMedical device
Olympus Corporation of the Americas recalls Olympus JF-140F duodenoscopes (Model NumberJF-140F)
Olympus recalls JF-140F duodenoscopes due to reported patient infections from improper cleaning. New reprocessing steps are required to reduce infection risk.
OlympusMay 11, 2018 - Lower riskMedical device
Smith & Nephew, Inc. recalls Birmingham Hip Resurfacing Acetabular Cup with Impactor: (a) Size 56 mm, REF 74120156 (b) Size 64 mm, REF 74120164 (c)
Smith & Nephew recalls specific hip cup models in the US that lack required FDA labeling, potentially causing confusion during use. Affected units include sizes 54-64mm with certain reference numbers and lots.
Smith & NephewMay 11, 2018 - Lower riskMedical device
Olsen Medical recalls Symmetry Olsen bipolar cord: (a) Bipolar Cord, Twin Pin Connector to Shrouded Instrument Connector, 12' (3.6m), REF
Olsen Medical recalls Symmetry bipolar cords with twin pin connectors that may encroach into sterile pouch seals, increasing risk of seal compromise. Affected units include specific model numbers and quantities listed in the recall notice.
Olsen MedicalMay 11, 2018 - UnratedDrug
L. Perrigo Company recalls Scopolamine Transdermal Therapeutic System, 1 mg/3 days, a) 4-count (NDC 45802-580-84); b) 10-count (NDC 45802-580-46);
Perrigo recalls specific Scopolamine Transdermal Therapeutic Systems (1 mg/3 days) due to defective delivery system. Affected products include 4-count and 10-count units with certain lot numbers. No remedy is stated in the recall notice.
PerrigoMay 11, 2018 - Stop using nowVehicle
THOMAS BUILT BUSES MINOTOUR (2018) recall — Structure
Thomas Built Buses recalls Minotour school buses because the rear emergency exit door may not open wide enough, limiting egress in an emergency.
Thomas Built BusesMay 10, 2018 - Use cautionVehicle
HYUNDAI IONIQ HYBRID (2018) recall — Hybrid Propulsion System
Hyundai is recalling 2017-2018 Ioniq Hybrids due to potential rear seat overheating and fire risk from electrical issues in the Power Relay Assembly.
HyundaiMay 10, 2018 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER HDX (2019) recall — Service Brakes, Air
Daimler Trucks North America recalls 2019 Thomas Built Saf-T-Liner HDX school buses with loose brake caliper mounting bolts that could reduce brake effectiveness and increase crash risk. Owners should contact DTNA for free brake bolt tightening.
Thomas BuiltMay 10, 2018 - Use cautionVehicle
INTERNATIONAL LT (2019) recall — Exterior Lighting
International LT trucks with specific Truck-Lite headlights may have incorrect 'VOL' markings instead of 'VOR' causing poor visibility. Recall started November 2018; fix involves installing a DOT VOR label.
Truck-LiteMay 10, 2018 - Use cautionVehicle
FREIGHTLINER CASCADIA (2019) recall — Service Brakes, Air
Daimler Trucks North America recalls 2018-2019 Freightliner Cascadia trucks with potentially loose brake caliper mounting bolts that could reduce brake effectiveness and increase crash risk. Owners should contact DTNA for free brake check.
Daimler Trucks North AmericaMay 10, 2018 - Use cautionVehicle
FREIGHTLINER CASCADIA (2019) recall — Steering
Daimler Trucks North America recalls certain 2019 Freightliner Cascadia vehicles due to potential steering wheel detachment causing loss of vehicle control. Owners must contact DTNA for free correction.
Daimler Trucks North AmericaMay 10, 2018 - UnratedMedical device
Mako Surgical Corporation recalls Rio System Irrigation Clip - Catalog # 111690 Product Usage: The RESTORIS Partial Knee Application (PKA) for use with
Mako Surgical recalls Rio System Irrigation Clip (Catalog #111690) for out of tolerance risk in RESTORIS Partial Knee Application procedures. Affected lots include 176364, 178346, 181337, 185213, 186561, 189709, 190559, 193643, and 195763A1.
Mako SurgicalMay 10, 2018 - Lower riskMedical device
Smiths Medical ASD Inc. recalls medfusion Stopcock, 1-way and 4-way, Model Numbers (REF): a. 081-101BE b. 081-101GE c. 081-101GEE d. 081-101NE e.
Smiths Medical recalls medfusion Stopcock 1-way and 4-way models with specific model and serial numbers due to lack of sterility assurance. Affected users should check their product details and contact Smiths Medical for guidance.
Smiths MedicalMay 10, 2018
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