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
34,960 found- Lower riskFood
Hank's Cheesecakes, LLC recalls Double Chocolate Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
Hank's Cheesecakes, LLC recalls Double Chocolate Cheesecake products for missing food allergen labels, which could cause allergic reactions. Consumers should check for the product description.
Hank's CheesecakeMay 31, 2019 - Use cautionFood
Bedessee Imports, Inc recalls National Heartland Naturals Premium Quality Pearl Barley 32 oz Plastic Bag, UPC 707966600083
Bedessee Imports recalls National Heartland Naturals Premium Quality Pearl Barley because it was mistakenly labeled gluten-free but contains gluten.
National Heartland NaturalsMay 31, 2019 - Use cautionVehicle
MAZDA CX-9 (2018) recall — Electrical System
Mazda recalls 2018 CX-9 vehicles with faulty wiring that may prevent passenger airbag deployment and turn signals from working, increasing crash risk. Owners must contact Mazda for free repairs.
MazdaMay 30, 2019 - Use cautionVehicle
SUBARU CROSSTREK (2019) recall — Visibility
Subaru is recalling certain 2019 Crosstrek vehicles with driver's side rear-door glass that may shatter into large pieces, posing an injury risk. Owners must have the window replaced free by dealers.
SubaruMay 30, 2019 - Use cautionVehicle
JAYCO GREYHAWK (2020) recall — Service Brakes, Air
Jayco is recalling 2020 Greyhawk motorhomes with potential brake relay valve air flow issues that could increase stopping distance, risking crashes. Owners must contact Spartan for free brake relay valve replacement.
JaycoMay 30, 2019 - Lower riskMedical device
Becton Dickinson & Company recalls BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number: 367001 Product Usage: Blood Alcohol
Becton Dickinson recalls BD Vacutainer Fluoride Tubes (Part 367001) for blood alcohol tests due to potential inaccurate results if stored over 2 days. Affected lots may need replacement to ensure accurate blood alcohol measurements.
Becton DickinsonMay 30, 2019 - Use cautionMedical device
Clinical Innovations, LLC recalls Clearview Total Uterine Manipulator (model UM750), The device is labeled in part, "ClearView(R) TOTAL, 7 cm* *
Clinical Innovations recalls UM750 uterine manipulators due to incorrect component causing potential surgery delays. Affected units have lot 181183. Contact for remedy details.
Clinical InnovationsMay 30, 2019 - Lower riskMedical device
Galemed Corporation recalls Babi.Plus Bubble PAP Valve with 12.5 cm H2O Pressure Relief Manifold, REF 1002, Rx Only, UDI: 24710810093559
Galemed recalls Babi.Plus Bubble PAP Valve with 12.5 cm H2O Pressure Relief Manifold (REF 1002) due to reports of gas venting below standard pressure. Affected units have specific UDI and lot numbers.
GalemedMay 30, 2019 - Lower riskMedical device
Boston Scientific Neuromodulation Corporation recalls Nitinol Thermocouple Electrode, 5cm - Product Usage: The TCN Electrode is indicated for use in RF heat lesioning of
Boston Scientific recalls certain Nitinol Thermocouple Electrodes (5cm) due to incorrect Instructions for Use packaging. This may lead to improper use of the device for nerve pain treatment.
Boston ScientificMay 30, 2019 - Lower riskMedical device
Medline Industries, Inc. recalls Anti-fog solution packaged in a Tyvek peel pouch and it is placed into various kits. Kit are labeled as follows:
Medline recalls anti-fog solutions in Tyvek pouches for surgical kits due to chemical degradation. Kits labeled with specific names like 'LAP CHOLE' or 'ROBOTICS' are affected. No remedy provided.
MedlineMay 30, 2019 - Lower riskMedical device
Ortho Development Corporation recalls Tibial Tray Nonporous A Size 2; Model # PN 162-1200-A; Material: Ti6Al4V.
Ortho Development Corporation recalls Tibial Tray Nonporous A Size 2 (Model PN 162-1200-A) due to a manufacturing defect that may cause resistance during assembly. Affected units include those with Lot Number A200590.
Ortho DevelopmentMay 30, 2019 - Lower riskMedical device
Paltop Advanced Dental Solutions Ltd recalls Paltop Advanced Plus Dental Implant Dia 6.0mm L10mm Catalog Number: 20-70024P
Paltop recalls specific dental implants due to inconsistent surface topography. Affected units may have unreliable surface texture, potentially impacting dental procedures. Contact for details.
PaltopMay 30, 2019 - Lower riskDrug
Surgery Pharmacy Services Inc recalls Memorial Central TPN. Rx Only, Rx # specific and Patient Specific volumes. Mixed by Surgery Pharmacy Serv., 3908
Surgery Pharmacy Services Inc recalls specific TPN products due to lack of sterility assurance. Patients must check RX numbers 311976-314888 for affected items.
Surgery Pharmacy Services IncMay 30, 2019 - Lower riskFood
Stonyfield Farm recalls Strawberry Banana Smoothie, 3.1oz, 6 pack, UPC Code 52159-70082
Stonyfield Farm recalls 6-packs of Strawberry Banana Smoothie due to mislabeled bottles with Very Berry Smoothie labels. The correct labeling is on individual bottles.
Stonyfield FarmMay 30, 2019 - Stop using nowConsumer product
Excel Industries Recalls Zero-Turn Mowers Due to Fire Hazard (Recall Alert)
Excel recalls zero-turn mowers with serial numbers 18058001-19028225 due to fire risk from a wire tie damaging the fuel line. Affected models include Hustler FasTrak, BigDog Stout, and BigDog Stout MP. Contact authorized dealers for free repairs.
Excel IndustriesMay 30, 2019 - Lower riskMeat & poultry
J Deluca Fish Company Inc. Recalls Siluriformes Products Produced Without Benefit of Import Inspection
USDA FSIS recalls 69,590 pounds of Vietnamese-sourced Siluriformes fish products that were not inspected before import. Consumers urged not to consume or dispose of items.
J Deluca Fish CompanyMay 29, 2019 - Use cautionVehicle
FORD F-550 (2018) recall — Equipment
VCI Emergency Vehicle Specialists recalls 2017-2018 Ford F-550 ambulances with ASA Electronics Voyager monitors that may reverse camera images, increasing crash risk. Owners notified and free repairs offered.
VCI Emergency Vehicle SpecialistsMay 29, 2019 - Stop using nowVehicle
HINO 338 (2019) recall — Equipment
ITI recalls Hino vehicles with ASA Voyager back-up cameras. The display may revert to factory settings, reversing the camera image and increasing crash risk.
ASA ElectronicsMay 29, 2019 - Use cautionVehicle
FORD F-450 (2019) recall — Equipment
LGE Coachworks recalls 2018-2019 Ford E-450/F-550 Freightliner M2 vehicles with ASA back-up camera displays that may reverse camera images, causing crashes. Owners must contact customer service for free replacement.
LGE CoachworksMay 29, 2019 - Use cautionMedical device
AtriCure, Inc. recalls EPi-Sense Guided Coagulation System with Visitrax, MOdel No. CDK-1413 - Product Usage: The EPi-Sense Guided Coagulation
AtriCure recalls EPi-Sense Guided Coagulation System with Visitrax model CDK-1413 due to potential compromised sterile package seal, which could lead to infection if used. Affected units include specific lots.
AtriCureMay 29, 2019 - Use cautionMedical device
Spectrum Medical Ltd. recalls Quantum Pump Console
Spectrum Medical recalls Quantum Pump Consoles with software version 6.2.1.9 due to potential unexpected shutdowns while in use. Affected units have specific serial numbers listed in the recall notice.
Spectrum MedicalMay 29, 2019 - Use cautionMedical device
Pega Medical Inc. recalls SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System
Pega Medical recalls SLIM Handle (catalogue # SLM-HND10:100) due to risk of jamming with the Driver component, potentially causing injury during orthopedic procedures.
Pega MedicalMay 29, 2019 - Use cautionMedical device
Fresenius Medical Care Renal Therapies Group, LLC recalls Liberty Cycler Cassettes (a disposable cassette that is intended to be used to perform peritoneal dialysis (APD) in
Fresenius Medical Care recalls Liberty Cycler Cassettes used in peritoneal dialysis due to potential leaks from damaged cassettes, risking contamination. Affected cassettes were sold with specific Liberty Cycler sets.
Fresenius Medical CareMay 29, 2019 - Lower riskMedical device
Siemens Healthcare Diagnostics Inc recalls Stratus CS Acute Care cTNI TestPak, SMN 10445071 Product Usage: In vitro diagnostic test for the measurement of cardiac
Siemens Healthcare recalls Stratus CS Acute Care cTNI TestPak due to potential for increased false positive results in cardiac troponin I tests. This may lead to incorrect heart attack diagnoses.
Siemens HealthcareMay 29, 2019 - Use cautionMedical device
Zyno Medical LLC recalls Zyno Medical Administration Set -105"ADMIN SET 20DP W/FILTER 2YSITES CLMP- For Use with Zyno Medical Infusion pumps or
Zyno Medical recalls 105" administration sets with inverted pinch clamps that may cause blood to be drawn from patients instead of delivering fluids during infusion. Affected units have specific product codes and lot numbers.
Zyno MedicalMay 29, 2019 - Stop using nowConsumer product
Target Recalls USB Charging Cables Due to Shock and Fire Hazards
Target recalls heyday : purple/green/blue iridescent 3-foot Lightning USB cables that can cause shock or fire if metal contacts charger prongs during use.
heydayMay 29, 2019 - Use cautionConsumer product
Aegean Apparel Recalls Children's Sleepwear Due to Violation of Federal Flammability Standard
Aegean Apparel recalls children's robes and pajama pants that fail federal flammability standards, risking burn injuries. Consumers should stop using and get a refund.
Aegean ApparelMay 29, 2019 - Lower riskMeat & poultry
Richwell Group, Inc. Recalls Siluriformes Products Produced Without Benefit of Import Inspection
USDA FSIS recalls 160,020 pounds of Siluriformes fish from Vietnam produced without import inspection. Consumers urged not to eat or dispose of products.
Maxfield SeafoodMay 28, 2019 - Lower riskMedical device
Nobel Biocare Usa Llc recalls Healing Abutment Conical Connection RP 0 3.6 x 5mm, REF: 36644, UDI: 07332747034462 - Product Usage: Dental implant
Nobel Biocare recalls dental healing abutments with incorrect size that could cause improper fit during implant procedures. Affected units have specific reference and UDI numbers.
Nobel BiocareMay 28, 2019 - Lower riskMedical device
Datascope Corporation recalls Sensation Plus 7.5Fr. 40cc Intra-Aortic Balloon Catheter with accessories, Part Number 0684-00-0568-01 Product Usage:
Datascope recalls Sensation Plus 7.5Fr 40cc Intra-Aortic Balloon Catheters with expired label due to reversed manufacture and expiry dates. Affected units may be used incorrectly.
DatascopeMay 28, 2019
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