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- Lower riskMedical device
Phadia Ab recalls EliA RF IgM Well, REF 14-5600-01 Product Usage: Usage: EliA RF IgM is intended for the in vitro quantitative
Phadia Ab recalls EliA RF IgM Well (REF 14-5600-01) due to potential for low assay results. Affected units may lead to inaccurate rheumatoid arthritis testing.
Phadia AbMay 10, 2019 - Use cautionMedical device
Medline Industries Inc recalls Centurion Convenience Kits, containing BD Alaris Pump Infusion Sets. BD code 11522558 (Centurion code 110931) contained
Medline recalls Centurion Convenience Kits with BD Alaris Pump Infusion Sets (BD code 11522558) due to silicone tubing defects that may cause over-infusion of medication. Affected kits include specific model numbers and production lots.
MedlineMay 10, 2019 - Use cautionMedical device
Cadence Science, Inc. recalls Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340
Cadence Science recalls glass syringes that may break during use, posing a risk of injury. Affected models include Part Nos. 5338-5343 with specific GTINs. Consumers should stop using and contact for replacement.
Cadence ScienceMay 10, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls Leadwire sets with snap ends: REF/Catalog Number Description 2106381-001 ECG Leadwire set, 5-lead, snap, AHA, 74 cm/ 29
GE Healthcare recalls 5-lead and 3-lead ECG leadwire sets with snap ends that may reduce defibrillation energy delivery, risking failed heart rhythm treatment during emergencies.
GE HealthcareMay 10, 2019 - Lower riskMedical device
Cardiocommand Inc. recalls CardioCommand, Inc. Transesophageal Cardiac Pacing and Recording System, Model 7A, REF 0101 - Product Usage:
Cardiocommand Inc. recalls Model 7A Transesophageal Cardiac Pacing System due to possible battery contact corrosion. Affected units have serial numbers 8059, 8060, 8022, 8063, 8211. Contact for remedy details.
CardiocommandMay 10, 2019 - UnratedDrug
Ecolab Inc recalls QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol), packaged in 7 oz cans, Ecolab, 370 Wabasha Street N, St.
Ecolab recalls QUIK-CARE Aerosol Foam Hand Sanitizer (7 oz cans) due to incorrect alcohol ingredient. Stop using if you have this product to avoid potential health risks.
EcolabMay 10, 2019 - Lower riskMedical device
Abbott Laboratories recalls Emerald Diluent Tubing, List number 09H50-01, accompanying CELL-DYN Emerald instrument, List number 09H39-01. The firm
Abbott recalls Emerald Diluent Tubing (lot 2018-10-16) that may show cloudiness or powder, leading to false high platelet counts in blood tests. Affected units include specific instrument serial numbers.
AbbottMay 9, 2019 - UnratedMedical device
I.T.S. GmbH recalls Rim Plate, 10-Hole, Left, PRS RX System. Titanium, implantable - Product Usage: The implant temporarily stabilizes bone
I.T.S. GmbH recalls Rim Plate, 10-Hole, Left, PRS RX System with incorrect laser marked article number. This implant stabilizes bone temporarily until consolidation. Affected units have model 21206-10 and lot 26/F42778.
I.T.S. GmbHMay 9, 2019 - Lower riskDrug
American Health Packaging recalls Anastrozole Tablets, USP, 1mg, 30-count unit dose blisters per carton, Rx Only, Packaged and Distributed by: American
American Health Packaging recalls 1mg Anastrozole tablets (NDC 60687-112-21) due to potential cross contamination from cleaning procedure failures. Affected lots expired by 08/31/2019 and 03/31/2020.
American Health PackagingMay 9, 2019 - Lower riskDrug
American Health Packaging recalls Anastrozole Tablets, USP, 1 mg, a) 30-count (NDC 68001-155-04) and 1000-count (NDC 68001-155-08) bottles, Rx Only,
American Health Packaging recalls 30-count and 1000-count Anastrozole Tablets (NDC 68001-155-04 and 68001-155-08) manufactured with potential cross contamination risks. Rx only products affected by GMP deviations in cleaning procedures.
American Health PackagingMay 9, 2019 - Lower riskFood
Young Ocean, Inc recalls Young Ocean brand Seasoned Alaskan Pollock Roe, frozen, wrapped in plastic liner and packed in styrofoam box, and
Young Ocean recalls Seasoned Alaskan Pollock Roe due to missing lactose and bonito ingredients on label. This affects frozen pollock roe sold in cardboard boxes with 20 packs per box. Consumers should check labels for missing allergens.
Young OceanMay 9, 2019 - Lower riskFood
DESHI DISTRIBUTORS, LLC recalls Deshi Golden Raisin, packaged in 3.5 oz, 7 oz. and 14 oz. clear plastic
Deshi Golden Raisins packaged in 3.5oz, 7oz, and 14oz clear plastic containers have been recalled due to elevated sulfites. Consumers should check UPC codes for affected products.
DeshiMay 9, 2019 - Stop using nowConsumer product
South Shore Furniture Recalls Chest of Drawers Due to Serious Tip-Over and Entrapment Hazards; One Fatality Reported
South Shore recalls Libra 3-drawer chests that can tip over and trap children, causing injury or death. Consumers must anchor chests to walls or return them for refunds.
South ShoreMay 9, 2019 - Stop using nowConsumer product
Imagine Nation Books Recalls Wireless Charging Pads Due to Burn Hazard
Imagine Nation Books recalls Pro Charge Power and Sharper Image Wireless Charging Pads due to burn risk from overheating. Consumers must stop using and get a refund.
Imagine Nation BooksMay 9, 2019 - Use cautionConsumer product
Havertys Recalls Entertainment Hutches Due to Injury Hazard
Havertys recalls Beckley Entertainment Hutches with weathered charcoal or dovetail gray finishes due to risk of top shelf falling and causing injury.
HavertysMay 9, 2019 - Use cautionVehicle
HARLEY-DAVIDSON FLHTK (2019) recall — Visibility
Harley-Davidson recalls 2019 FLHTK motorcycles with missing rear red reflectors that fail federal safety standards. Owners must have reflectors installed by dealers to prevent crashes.
Harley-DavidsonMay 8, 2019 - Use cautionVehicle
FORD EXPLORER (2020) recall — Power Train
Ford is recalling certain 2020 Explorer vehicles due to a power train issue that may cause the vehicle to roll away without warning, increasing crash risk. Owners must have the MPR cover installed and ensure the instrument cluster is not in Factory Mode.
FordMay 8, 2019 - Lower riskMedical device
Madison Polymeric Engineering recalls First Step Draco Pad, Product Number EP-4D
Madison Polymeric Engineering recalls First Step Draco Pad (EP-4D) due to contamination with Stenotrophomonas lactiubi. Affected units include specific lot numbers from December 2019.
Madison Polymeric EngineeringMay 8, 2019 - Lower riskMedical device
Xhale Assurance, Inc. recalls Nasal Alar SpO2 Sensor, Adult/Pediatric SpO2 Sensor, Rx Only Product Usage: The Assurance¿ Nasal Alar SpO2 Sensor is
Xhale recalls adult/pediatric SpO2 sensors with missing instructions for checking and changing the application site. This affects specific lot numbers and models sold from 2018 onward.
XhaleMay 8, 2019 - Use cautionConsumer product
Igloo Recalls Marine Coolers Due to Entrapment and Suffocation Hazards
Igloo recalls Marine Elite coolers with stainless-steel latches that can lock shut, trapping users inside. Consumers must keep coolers out of children's reach and contact Igloo for free latch replacement.
IglooMay 8, 2019 - Use cautionMeat & poultry
Santa Fe Importers, Inc. Recalls Ready-To-Eat Chicken Products due to Misbranding and an Undeclared Allergen
USDA FSIS recalls 1,589 pounds of ready-to-eat chicken meatballs due to soy allergen not declared on labels. Consumers urged not to consume and dispose of products.
Santa Fe ImportersMay 7, 2019 - Use cautionVehicle
FORD FOCUS (2017) recall — Fuel System, Gasoline
Ford recalls 2017 Focus vehicles with 2.0L GDI engines due to potential engine stall without warning, increasing crash risk. Owners must contact Ford for reprogramming and repairs.
FordMay 7, 2019 - Use cautionVehicle
MAZDA MAZDA3 (2019) recall — Seats
Mazda recalls 2019 Mazda3 vehicles with loose head restraints that may not lock properly during crashes, risking injury. Owners must contact Mazda for free spacer installation.
MazdaMay 7, 2019 - Lower riskFood
Twin City Foods Inc. recalls Signature Kitchens Green Peas & Diced Carrots; Net Wt 16 oz (1 lb) 453 g; UPC 2113009154; frozen
Twin City Foods recalls 16oz frozen green peas and diced carrots due to potential Listeria monocytogenes contamination. Consumers should check UPC 2113009154 and discard if expired.
Twin City FoodsMay 7, 2019 - Use cautionFood
Mecox Bay Dairy recalls Mecox Bay Dairy Sunrise Raw Milk Cheese in plastic wrap code L 2148 Size Range between .25 lb to 3 lb portions of a 3
Mecox Bay Dairy recalls Sunrise Raw Milk Cheese with plastic wrap code L 2148 due to Listeria Monocytogenes found in sampling. Consumers should check product labels for the code.
Mecox Bay DairyMay 7, 2019 - Use cautionVehicle
FORD F-550 (2018) recall — Equipment
Farber is recalling 2018 Ford F-550 trucks with ASA Electronics Voyager monitors that may reverse camera images, increasing crash risk. Owners must contact dealers for free harness relay capacitor modules.
FarberMay 6, 2019 - Use cautionVehicle
AUDI Q5 (2019) recall — Wheels
Volkswagen recalls 2018-2019 Audi Q5/SQ5 vehicles with loose wheel arch trim that may detach, causing crashes. Owners must contact VW for free repair.
VolkswagenMay 6, 2019 - Use cautionVehicle
THOR MOTOR COACH OMNI (2020) recall — Electrical System
Thor Motor Coach is recalling 2019-2020 Omni motorhomes with model BB35 or BH35 due to wires contacting an extra screw, risking electrical shorts and fire. Owners must have the junction box inspected and repaired free of charge.
Thor Motor CoachMay 6, 2019 - Lower riskMedical device
Qiagen Sciences, Inc. recalls RNeasy DSP FFPE Kit (48), REF 73604 - Product Usage: The RNeasy DSP FFPE Kit is a system intended for the purification
Qiagen recalls RNeasy DSP FFPE Kit (48) REF 73604 due to a contaminant in deparaffinization solution causing reduced RNA yields. Affected lots include 163016105. Users should contact Qiagen for details.
QiagenMay 6, 2019 - Use cautionMedical device
Becton Dickinson & Company recalls Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930,
Becton Dickinson recalls Alaris Pump Infusion Sets with specific model codes due to potential medication delivery errors. Affected units may cause unintended medication delivery or faster-than-expected drug flow.
Becton DickinsonMay 6, 2019
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