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- Lower riskMedical device
Zimmer Dental Inc recalls Outer Package Label: Tapered Screw-Vent Implant System, 4.1mm X 10mm, 3.5mm, REF:TSVM4B10, Sterile:R, Rx Only; Inner
Zimmer Dental recalls implant systems with incorrect inner package labeling. The outer package has correct item/lot numbers but the inner package shows wrong details. Consumers should check labels and contact Zimmer Dental for verification.
Zimmer DentalMay 10, 2018 - Lower riskMedical device
Life Technologies, Corp. recalls GIBCO CTS AIM V Serum-Free Media (SFM), Model Number 0870112BK. Tissue and cell culture medium.
Life Technologies recalls GIBCO CTS AIM V Serum-Free Media (Model 0870112BK) due to potential leaks causing mold growth in tissue culture media. Affected lots may need replacement to prevent contamination.
Life TechnologiesMay 10, 2018 - Lower riskMedical device
Anika Therapeutics, Inc. recalls Hyalomatrix, Product nos. 651105, 651103, 651104, and 651301 Product Usage: Hyalomatrix is a bi-layered, sterile,
Anika Therapeutics recalls Hyalomatrix wound dressings (product numbers 651105, 651103, 651104, 651301) due to potential packaging degradation during sterilization that could compromise product integrity over time.
Anika TherapeuticsMay 10, 2018 - Use cautionMedical device
FHC, Inc. recalls microTargeting" STar" Drive System (Manual), Product Number ST-DS-MA
FHC recalls microTargeting STar Drive System (Product Number ST-DS-MA) due to depth stop adapter risk of lead damage causing short circuits or requiring surgical repair.
FHCMay 10, 2018 - Lower riskMedical device
Angiodynamics Inc. (Navilyst Medical Inc.) recalls CAN 5F SINGLE XCELA PICC, Catalog Number 60M701531
Angiodynamics recalls CAN 5F SINGLE XCE:LA PICC kits with potential bacterial endotoxins. Affected units have specific catalog and lot numbers. Consumers should contact for details.
AngiodynamicsMay 10, 2018 - Lower riskFood
Caudill Sprouting LLC recalls Alfalfa Seeds
Caudill Sprouting LLC recalls alfalfa seeds linked to multistate Salmonella Montevideo and Cubana infections. Consumers should avoid these seeds to prevent foodborne illness.
Caudill SproutingMay 10, 2018 - Stop using nowConsumer product
Tobi Recalls Babynest Crib Bumpers Due to Strangulation Hazard; Sold Exclusively Online at babybay.us (Recall Alert)
Babynest crib bumpers sold online at babybay.us pose strangulation hazard due to long strings. Consumers must stop using and get full refunds.
BabynestMay 10, 2018 - Stop using nowConsumer product
Munchkin Recalls Waterpede Bath Toys Due to Choking Hazard
Munch: Waterpede bath toys can break apart, exposing small parts that pose a choking hazard to young children. Consumers should stop using and contact Munchkin for a free replacement.
MunchkinMay 10, 2018 - Stop using nowConsumer product
illy Recalls 8.8-Ounce Whole Bean Coffee Cans Due to Injury Hazard
illy recalls 8.8-oz whole bean coffee cans due to a lid detachment injury hazard. Check your can's bottom for an air valve and best-by date.
illyMay 10, 2018 - Stop using nowConsumer product
ALDI Recalls Deep Fryers Due to Fire and Burn Hazards
ALDI recalls Ambiano mini deep fryers with fire and burn risks. Stop using and return for refund.
ALDIMay 10, 2018 - Use cautionVehicle
TOYOTA PRIUS (2018) recall — Electrical System
Toyota recalls 2018 Prius vehicles with potential electrical short causing fire risk. Free repair includes replacing engine wire harness assembly and protective sleeve.
ToyotaMay 9, 2018 - Use cautionVehicle
MITSUBISHI OUTLANDER (2019) recall — Equipment
Mitsubishi recalls 2018-2019 Outlanders with incorrect rear wheel rim size labels, risking non-compliance with safety standards. Owners must get a corrected label to avoid crash risks.
MitsubishiMay 9, 2018 - Use cautionVehicle
INTERNATIONAL LONESTAR (2019) recall — Engine And Engine Cooling
Navistar recalls 2017-2019 International trucks with Cummins engines due to risk of fuel line bursting on steep declines, potentially causing leaks and vehicle stalling. Owners must have fuel line replaced by dealers.
NavistarMay 9, 2018 - Lower riskMedical device
Ortho-Clinical Diagnostics recalls VITROS Chemistry Products PHYT Slides, Catalog Number 8298671. in vitro diagnostic
Ortho-Clinical Diagnostics recalls VITROS PHYT Slides (Catalog 8298671) due to potential imprecise test results. Affected lots may cause inaccurate quality control and patient samples.
Ortho-Clinical DiagnosticsMay 9, 2018 - Use cautionMedical device
B. Braun Medical, Inc. recalls Space Pump IV Set, 2 Caresites, ASV, 0.2 Micron Air Eliminating Filter, Product Code 363420 The Infusomat Space Pump IV
B. Braun recalls Space Pump IV sets with potential for incorrect filter that lacks air elimination. Affected units have lot number 0061583973. Consumers should check their IV sets for the filter and contact B. Braun for details.
B. BraunMay 9, 2018 - Use cautionMedical device
Johnson & Johnson Surgical Vision Inc recalls OptiMedica Catalys Precision Laser System, CE 0044 containing software cOS 5.00.33 Product Label for Serial Numbers:
Johnson & Johnson recalls OptiMedica Catalys Precision Laser Systems with specific software versions due to potential mismatch in plastic hemisphere cuts during daily alignment verification, affecting cataract surgery procedures.
OptiMedicaMay 9, 2018 - Use cautionMedical device
Konica Minolta Medical Imaging USA, Inc. recalls CS-7, Model No. A4C1
Konica Minolta recalls CS-7 Model A4C1 laptops due to possible battery fire risk. Affected units may require BIOS updates to reduce fire risk.
Konica Min: A4C1May 9, 2018 - Use cautionFood
Raley's Family of Fine Stores recalls Raley's Peanut Butter Brownies 6 Ct.; NET WT: 16 oz. 1 lb. UPC: 46567-61806
Raley's recalls Peanut Butter Brownies because peanuts are not listed in the Contains Statement, posing an allergy risk. Check your UPC and sell-by dates.
Raley'sMay 9, 2018 - Stop using nowConsumer product
Women’s Scarves Recalled by Wrapables Due to Violation of Federal Flammability Standard (Recall Alert)
Wrapables is recalling 100% silk women's scarves sold online due to flammability issues. Consumers should stop using and get a refund from Wrapables.
WrapablesMay 9, 2018 - Stop using nowConsumer product
Specialized Bicycle Components Recalls Bicycles with Stout Cranks Due to Fall and Injury Hazards
Specialized recalls bicycles with Stout cranks from 2017 that can disengage, causing falls and injuries. Affected models include Fuse Comp and Fatboy SE with specific color combinations and serial codes starting with '17'.
SpecializedMay 9, 2018 - Use cautionMedical device
Stryker Sustainability Solutions recalls Reprocessed HARMONIC Ace¿ +7, 5mm Diameter Shears with Advanced Hemostasis (HARH), Item Number HARH36 Product Usage:
Stryker recalls reprocessed HARMONIC Ace+7 shears that may show 'No Instrument Uses Remaining' error code, preventing use. Affected units may need replacement.
StrykerMay 8, 2018 - Use cautionMedical device
Wescam Inc recalls MX-10 surveillance laser system Product Usage: The expected usage of the product is to facilitate observation and
Wescam recalls MX-10 surveillance laser systems with a longer-than-specified ocular hazard distance, risking light exposure beyond safe limits. Affected units include specific part numbers sold for observation missions.
WescamMay 8, 2018 - UnratedMedical device
Human Design Medical Llc recalls Vivo 65, Continuous Ventilator, Home Use, Cat. No. 204000 Product Usage: To provide continuous or intermittent
Human Design Medical recalls Vivo 65 home ventilators with unreleased firmware upgrade tools. This could pose risks during use. Affected units may need to stop using until a fix is provided.
Human Design MedicalMay 8, 2018 - UnratedMedical device
MEDTECH SAS recalls ROSA(TM) Robotized Stereotactic Assistant, Version 2.5 ROSA Surgical Device is a computer-controlled electromechanical
MEDTECH SAS recalls ROSA Robotized Stereotactic Assistant Version 2.5 due to outdated device approval. Affected units have specific serial numbers listed. No remedy is provided in the recall notice.
MEDTECH SASMay 8, 2018 - Use cautionMedical device
Zeiss, Carl Inc recalls Cell Observer SD, DirectFRAP, Laser TIRF 1, Laser TIRF 2, Laser TIRF3, LightSheet, Elyra, and multiple Laser Scanning
Zeiss recalls several laser scanning microscopes due to potential laser beam leakage in certain eyepiece configurations, which could exceed Class I safety limits.
ZeissMay 8, 2018 - Lower riskMedical device
Luminex Corporation recalls Verigene Enteric Pathogens Nucleic Acid Test (EP) for detecting and identification of pathogenic enteric bacteria,
Luminex recalls Verigene Enteric Pathogens Nucleic Acid Test kits with specific cartridge model due to risk of false Yersinia enterocolitica results. Affected units include lot 032718023A.
LuminexMay 8, 2018 - Use cautionMedical device
Vyaire Medical recalls AirLife Resuscitation Device, Adult labeled as the following: a. Adult, with mask, oxygen reservoir bag, Part Number
Vyaire Medical recalls AirLife Resuscitation Devices with potential airflow obstruction during oxygen delivery. Affected models include specific part numbers and lot numbers for adult use. Consumers should check their device details to determine if recalled.
Vyaire MedicalMay 8, 2018 - Lower riskMedical device
Dynarex Corporation recalls Dynarex CGA870 All Brass Oxygen Regulator, All Brass - 0-25 LPM, Barb & 2-DISS Outlet, UPC: 616784522715, Model Number
Dynarex recalls CGA870 oxygen regulators with inaccurate flow rate indicators. This may affect medical gas delivery accuracy. Contact Dynarex for details.
DynarexMay 8, 2018 - UnratedMedical device
Exactech, Inc. recalls Optetrak Logic CC Stem Extension, 22mm x 160mm The OPTETRAK Logic CC Total Knee System is indicated for use in
Exactech recalls Optetrak Logic CC Stem Extension (22mm x 160mm) due to potentially non-conforming internal threads. Affected units sold with serial number 5370045.
ExactechMay 8, 2018 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), infusion pump, 35700BAX2 Product Usage: The
Baxter recalls SIGMA Spectrum Infusion Pumps with Master Drug Library (Version 8) due to 12.5-inch hangers supplied with secondary sets, which may not lower primary bag 20 inches below secondary bag as required. This could affect infusion safety.
BaxterMay 8, 2018
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