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
34,959 found- Use cautionMedical device
Edwards Lifesciences, LLC recalls EV1000 Clinical Platform, Models: EV1000A, EV1000NI, EV1000CS Product Usage: EV1000A Monitor is used to optimize fluid
Edwards Lifesciences recalls EV1000A, EV1000NI, and EV1000CS monitors for potential fire risk from liquid entering AC power outlets. Affected units may need replacement.
Edwards LifesciencesMar 21, 2019 - Lower riskMedical device
Community Products, LLC recalls Rifton TRAM Standard Base, SKU K310, powered lift device
Community Products recalls Rifton TRAM Standard Base (SKU K310) due to design change in load-bearing buckle causing spring fatigue failure after repeated use. Affected units have specific ID codes listed in the recall.
Community ProductsMar 21, 2019 - Use cautionMedical device
ROi Consolidated Service Center (CSC) recalls Regard ¿ custom surgical pack labeled as "LAPAROSCOPIC - OSU" including recalled Stryker part numbers 0620 040 660
ROi recalls laparoscopic surgical packs with Stryker tube sets that may detach, causing gas leaks or hissing sounds. Affected units include specific part numbers and lot codes.
ROiMar 21, 2019 - Lower riskMedical device
Conmed Corporation recalls ConMed Anchor Tissue Retrieval System 10 MM, 235 ML, (5/BX) Catalog Number: TRS100SB2 The Anchor Tissue Retrieval
ConMed recalls specific surgical pouches due to potential sterility compromise from seal defects. Affected units manufactured between April 2018 and February 2019 with certain lot codes.
ConMedMar 21, 2019 - Use cautionFood
Better Made Snack Foods Inc. recalls Better Made Snack Foods Family Size $3.99 Original Potato Chips 10oz. flexible pouch bag UPC code of 041633063048 12
Better Made recalls 10oz potato chips with undeclared milk. Check UPC 041633063048 for affected lots. Stop using if you have these chips.
Better Made Snack FoodsMar 21, 2019 - Stop using nowFood
Allen's Blueberry Freezer, Inc. recalls Wild Sweet ALLEN'S BLUEBERRIES WILD BLUEBERRIES IQF 30 LBS. NET 13.6 Kg. Packaged in a corrugated carton. Keep frozen
Allen's Blueberry Freezer recalls 37,800 lbs of Wild Sweet wild blueberries due to potential E. coli O157:H7 contamination.
Wild SweetMar 21, 2019 - Stop using nowFood
Impossible Foods recalls Impossible Foods Bulk, 5 lb. vacuum sealed plastic-pack. Keep Frozen; This is a plant product that is looks like and is
Impossible Foods recalls 5 lb. vacuum-sealed bulk plant meat due to a plastic piece found in the product. Keep frozen until June 19, 2019.
Impossible FoodsMar 21, 2019 - Stop using nowConsumer product
Bulk Unlimited Recalls Children's Globes Due to Fire and Burn Hazards (Recall Alert)
Bulk Unlimited recalls Little Experimenter children's globes sold online due to overheating wires that pose fire and burn risks. Contact for a free replacement.
Bulk UnlimitedMar 21, 2019 - Stop using nowConsumer product
Alpha Guardian Recalls Stack-On Gun Safes Due to Lock Failure and Injury Hazard
Alpha Guardian recalls Stack-On Sentinel gun safes due to lock failure that could allow unauthorized access to firearms, posing an injury hazard. Consumers must stop using and contact for free replacement or refund.
Alpha GuardianMar 21, 2019 - Use cautionConsumer product
Air King America Recalls Wall-Mounted Range Hoods Due to Injury Hazard
Air King recalls Valencia wall-mounted range hoods with potentially inadequate wall mounting anchors that could cause injury. Consumers should stop using and inspect units for recall details at www.airkinglimited.com/recall.
Air KingMar 21, 2019 - Use cautionVehicle
MERCEDES-BENZ SPRINTER 2500 (2018) recall — Unknown Or Other
Mercedes-Benz recalls 2018-2019 Sprinter and Metris vehicles due to missing final quality inspections on safety parts. Check if your VIN is affected.
Mercedes-BenzMar 20, 2019 - Use cautionVehicle
HONDA ODYSSEY (2019) recall — Service Brakes, Air
Braun recalls 2018-2019 Honda Odyssey vehicles with wheelchair ramp conversions due to potential brake system failure. The anti-lock brakes may not work properly, increasing crash risk. Owners should contact Braun for free repairs.
BraunMar 20, 2019 - Use cautionVehicle
VOLKSWAGEN PASSAT (2020) recall — Air Bags
Volkswagen recalls 2020 Passat vehicles with potential side airbag deployment failure in crashes. Owners must have airbags inspected and replaced free by April 2019.
VolkswagenMar 20, 2019 - Use cautionVehicle
IC BUS CESB (2020) recall — Fuel System, Diesel
Navistar recalls certain 2017-2020 diesel trucks and buses with Cummins B6.7 engines that may overheat and cause fire. Owners must contact customer service for free fuel heater replacement.
NavistarMar 20, 2019 - Use cautionVehicle
IC BUS CESB (2020) recall — Fuel System, Diesel
Navistar recalls 2017-2020 IC Bus CESB school buses with Cummins B6.7 diesel engines and specific fuel modules due to fire risk from overheating fuel heaters.
NavistarMar 20, 2019 - Lower riskMedical device
GETINGE US SALES LLC recalls Maquet Servo-I Ventilator System -EDI CATHETER PHT Free 6Fr/49cm 5/pkg Product Code/REF Number: 6685775 Product Usage:
GETINGE recalls Maquet Servo-I Ventilator Edi Catheter with incorrect expiry date on single packs. This may lead to improper use of the catheter for monitoring diaphragm activity or feeding. Contact for replacement or return.
GETINGEMar 20, 2019 - Lower riskMedical device
Ortho-Clinical Diagnostics recalls VITROS XT 7600 Integrated System, with V3.4 or 3.4.1 SW Product Code: 6844461 Product Usage: INTENDED USE: For in vitro
Ortho-Clinical Diagnostics recalls VITROS XT 7600 Integrated System with V3.4 or 3.4.1 software (product code 6844461) due to potential for incorrect test results. Affected units have serial numbers 76000108 through current.
Ortho-Clinical DiagnosticsMar 20, 2019 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Siemens Digital Linear Accelerators of type: ARTISTE MV System MEVATRON M2/Primus Mid-Energy PRIMUS PRIMUS HI ONCOR
Siemens recalls certain digital linear accelerators where disabling the AMP function may cause patient or user injury due to collision with LINAC equipment. Affected units include ARTISTE, ONCOR, and PRIMUS models with specific software versions.
SiemensMar 20, 2019 - Lower riskMedical device
GE Healthcare, LLC recalls NM/CT 870 CZT, Model/Catalogue/Code # H3906CW Product Usage: The GE Discovery NM/CT 670 CZT system is intended for
GE Healthcare recalls certain NM/CT 670 CZT systems due to potential loss of detector mounting redundancy during installation, which could affect nuclear medicine imaging safety.
GE HealthcareMar 20, 2019 - Stop using nowFood
Century Snacks LLC recalls Snak Club Honey Bliss Nut Mix: Honey Butter Flavored Almonds, Peanuts, Pumpkin Seeds, Pistachios, Pecans & Honey Sesame
Century Snacks LLC recalls Snak Club Honey Bliss Nut Mix due to undeclared milk allergen. Check your packaging for specific UPCs and lot codes.
Snak ClubMar 20, 2019 - Stop using nowFood
Kingston Pharma LLC recalls DG health NATURALS For Infants 2+ Months+ baby Cough Syrup + Mucus, Natural Grape Flavor, 2 FL OZ (59 mL), UPC: 8 54954
Kingston Pharma recalls infant cough syrup with Bacillus bacteria contamination. Stop using immediately due to potential health risks.
Kingston PharmaMar 20, 2019 - Stop using nowConsumer product
Kubota Recalls Zero Turn Mowers Due to Fire Hazard (Recall Alert)
Kubota recalls 2018-2019 ZD100 series zero turn mowers due to fire risk from throttle cable contacting internal wiring. Affected units have specific serial numbers and are orange/black. Contact Kubota for free repair.
KubotaMar 20, 2019 - Stop using nowConsumer product
American Honda Recalls Portable Generators Due to Fire and Burn Hazards
Honda recalls EU2200i, EU2200i Companion and EB2200i portable generators due to gasoline leaks from fuel valves causing fire and burn risks. Affected units sold with red or camo covers; contact Honda for free repair.
HondaMar 20, 2019 - Stop using nowMeat & poultry
La Rosita Fresh Market Inc. Recalls Ground Beef Products due to Possible E. coli O157:H7 Contamination
La Rosita Fresh Market recalls ground beef due to possible E. coli O157:H7 contamination. Do not consume; discard or return immediately.
La Rosita Fresh MarketMar 19, 2019 - Lower riskMedical device
Stryker Instruments Div. of Stryker Corporation recalls Performance Series Sagittal Blade, Catalog Number 6125-127-100 Product Usage: The Stryker Heavy Duty Sagittal Blades
Stryker recalls heavy duty sagittal blades (catalog 6125-127-100) due to potential sterility breach during manufacturing. Affected units may not be sterile, risking infection during surgery.
StrykerMar 19, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls AIR Technology Anterior Array, Catalogue Numbers: (a) 5746694, (b) 5746695, (c) 5746696, a receive-only RF coil
GE Healthcare recalls AIR Technology Anterior Array RF coils (catalog numbers 5746694-5746696) due to potential separation of the outer seam exposing porous material that cannot be disinfected, risking user or patient contact with infectious agents.
GE HealthcareMar 19, 2019 - Lower riskMedical device
Collagen Matrix, Inc. recalls Neomem Resorbable Collagen Membrane, 15 mm x 20 mm Reference Number (model): N1520 - Product Usage: Neomem is a
Collagen Matrix recalls Neomem Resorbable Collagen Membrane (N1520) due to incorrect packaging. This may lead to improper use in dental procedures. Affected units include specific lot numbers.
Collagen MatrixMar 19, 2019 - Lower riskMedical device
Aniara Diagnostica LLC recalls BIOPHEN UFH Control C1, REF 224101
Aniara Diagnostica recalls BIOPHEN UFH Control C1 devices with specific lot numbers due to incorrect Instructions for Use packaging. Affected units may have improper instructions that could lead to improper use.
Aniara DiagnosticaMar 19, 2019 - Lower riskMedical device
Carestream Health, Inc. recalls OnSight 3D Extremity System- X-Ray, Tomography Computed System Catalog Numbers: 1743566 (w/ Attached Console) 1743574
Carestream Health recalls OnSight 3D Extremity X-Ray Systems with specific catalog numbers due to potential patient data transfer errors during re-assignment of parent/companion pairs.
Carestream HealthMar 19, 2019 - UnratedDrug
Allergan Sales, LLC recalls Combigan (brimonidine tartrate/timolol maleate ophthalmic solution) 0.2%/0.5% 5 mL bottles, Rx only, Allergan, Inc.
Allergan Sales, LLC is recalling specific lots of Combigan ophthalmic solution due to current Good Manufacturing Practice deviations. Check your bottle's lot number.
AllerganMar 19, 2019
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