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- Use cautionFood
Meninno Brothers Gourmet Foods recalls Hannaford brand 20 oz. traditional quiche w/tomatoes, cheese and basil in flexible plastic with round top and bottom.
Hannaford recalls 20 oz traditional quiche due to missing ingredient and allergen statements on the label. Check your lot codes.
HannafordJul 24, 2019 - Lower riskFood
SIGA LOGISTICS S DE RL DE CV recalls SIGA Fresh Basil, 1 lb bag, 10 plastic bags (1 lb bag) per carton
SIGA recalls 1 lb bags of fresh basil due to potential Cyclospora contamination. Consumers should check product dates and contact SIGA for details.
SIGAJul 24, 2019 - Lower riskFood
CH Guenther & Sons, Inc recalls Winco Foods, Taco Seasoning Mild, Net Wt. 1.25 OZ, Distributed by Winco Foods, LLC, Boise, ID, UPC 0 70552 90126 1
Winco Foods' 1.25 oz mild taco seasoning (UPC 070552901261) may contain Salmonella. Consumers should check labels and contact Winco for details.
CH Guenther & SonsJul 24, 2019 - Use cautionConsumer product
Trek Recalls Kickster Bikes Due to Fall Hazard
Trek recalls 2013-2019 Kickster bikes due to steer tube clamp breaking, risking falls for toddlers. Consumers must remove bikes from children and get free repairs.
TrekJul 24, 2019 - Stop using nowConsumer product
Porter Cable Table Saws Sold Exclusively at Lowe's Stores Recalled Due to Fire Hazard; Made by Chang Type
Porter-Cable 10-inch table saws sold at Lowe's are recalled due to fire hazards. Stop using immediately and contact Chang Type for a refund.
Porter-CableJul 24, 2019 - Use cautionVehicle
BMW X5 (2019) recall — Wheels
BMW recalls 2019 X5 vehicles with loose left wheel bolts that could detach, causing crashes. Owners must have bolts tightened by dealers free of charge.
BMWJul 23, 2019 - Lower riskMedical device
New Standard Device Inc recalls 'n'-Hole Post which is a component of the Revolution External Fixation System Catalog Numbers: 100801, 100802, 100803,
New Standard Device recalls 'n'-Hole Post components (catalogs 100801-100805) due to thread stripping during application. Affected users should check their device model and contact for remedy.
New Standard DeviceJul 23, 2019 - Lower riskMedical device
Aggredyne, Inc. recalls AggreGuide A-100 Instrument
Aggredyne recalls AggreGuide A-100 instruments with software versions 5.1 or 5.2 that may display 'Low' results due to a software error causing 0 RPM blood mixing. Affected units have serial numbers between xx0001 and xx0160.
AggredyneJul 23, 2019 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Mammomat Revelation with software version VC10 and Biopsy Option Intended Use: For mammography exams, screening,
Siemens recalls Mammomat Revelation mammography systems with software version VC10 and Biopsy Option due to rare workstation unresponsiveness during biopsies. Affected units may require software update or repair.
SiemensJul 23, 2019 - UnratedMedical device
Instrumentation Laboratory Co. recalls ROTEM ex-tem Canada Part No: 503-05-CA
Instrumentation Laboratory Co. recalls ROTEM ex-tem Canada Part No 503-05-CA with Lot # 42255801 due to prolonged clotting times. Affected users should contact for remedy.
Instrumentation Laboratory Co.Jul 23, 2019 - Lower riskMedical device
Roche Diagnostics Operations, Inc. recalls Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190 Analyzer/Module: cobas c 311 and cobas c 501/502
Roche recalls vancomycin testing devices that may give low sample results. Affected units include cobas c 311 and cobas c 501/502 analyzers with catalog # 06779336190.
RocheJul 23, 2019 - Lower riskMedical device
OMNIlife science Inc. recalls OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Insert Liner 51-28;
OMNIlife science recalls ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Insert Liner 51-28 due to potential higher wear rate leading to revision surgery.
OMNIlife scienceJul 23, 2019 - Lower riskDrug
Glenmark Pharmaceuticals Inc., USA recalls Mometasone Furoate Cream USP, 0.1%, packaged in a) 15gram tubes (NDC 68462-192-17) and b) 45 gram tubes (NDC
Glenmark Pharmaceuticals is recalling specific lots of Mometasone Furoate Cream USP 0.1% because complaints indicate the product has a gritty texture.
Glenmark PharmaceuticalsJul 23, 2019 - Stop using nowConsumer product
The Boppy Company Recalls Infant Head and Neck Support Accessories Due to Suffocation Hazard
Boppy recalls infant head and neck support accessories due to suffocation risk from improper positioning. Affected models 4150114 and 4150117 sold in Ebony Floral and Heathered Gray styles.
BoppyJul 23, 2019 - UnratedMedical device
DeRoyal Industries Inc recalls DeRoyal Enteral Safe Feeding Tubes: a) REF 54-2450R, 5 FR x 24" Polyurethane b) REF 54-2465R, 6.5 FR x 24" Polyurethane
DeRoyal recalls specific polyurethane feeding tubes due to connector detachment risk. Affected models include REF 54-2450R, 54-2465R, 54-2480R, and 54-3680R with certain lot numbers. No remedy is stated in the recall notice.
DeRoyalJul 22, 2019 - Lower riskMedical device
Zeus Scientific, Inc. recalls Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay File Software: ZEUS vl B. burgdorferi lgG-lgM.asy
Zeus Scientific recalls specific Dynex DSX software for false negative results in Lyme disease tests due to a programming error skipping well H6. Affected users should check their software versions and contact support.
Zeus ScientificJul 22, 2019 - Lower riskMedical device
GETINGE US SALES LLC recalls Getinge MCC Flow i Disposable CO2 absorber, used in anesthesia systems.
Getinge recalls MCC Flow i Disposable CO2 absorbers due to reversed expiration and manufacturing dates on labels. This affects anesthesia systems used in hospitals and clinics.
GetingeJul 22, 2019 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc recalls Siemens ADVIA Centaur Folate 100 test kit-for IVD of folate in serum or red blood cells SMN:10310308
Siemens Healthcare recalls ADVIA Centaur Folate 100 test kits for potential elevated folate results due to homocysteine assay interference. All lots are affected. No action needed as the issue is not a safety hazard.
Siemens HealthcareJul 22, 2019 - UnratedDrug
Wise Pharmacy recalls Papaverine/Phentolamine/Alprostadil 30 mg/2 mg/30 mcg/mL Injectable, 2.5 mL Vial, Rx only, Compounded by Wise Pharmacy,
Wise Pharmacy recalls specific compounded injectable medication batches due to lack of processing controls. Affected lots expire by July 2019. Consumers should contact the pharmacy for details.
Wise PharmacyJul 22, 2019 - Use cautionMeat & poultry
US Foods Recalls Raw Beef and Pork Products Due to Possible Product Contamination
US Foods recalls approximately 712 pounds of raw beef and pork products produced July 18, 2019, that may be contaminated. Products bear USDA inspection number EST. 21103 and were shipped to restaurants in Alabama, Florida, Georgia, Mississippi, and Tennessee. Consumers should discard or return these items to the place of purchase.
US FoodsJul 20, 2019 - Use cautionVehicle
GENESIS G80 (2018) recall — Engine And Engine Cooling
Hyundai recalls 2018 Genesis G80 vehicles with turbocharged engines due to oil leaking onto exhaust manifolds, increasing fire risk. Owners must have the turbocharger oil supply pipe replaced free of charge.
HyundaiJul 19, 2019 - Use cautionVehicle
KIA OPTIMA (2019) recall — Forward Collision Avoidance
Kia is recalling certain 2019 Optima vehicles with a software error in the Forward Collision-Avoidance Assist system that may prevent braking when a stationary vehicle is detected. Owners must contact Kia for a free software update.
KiaJul 19, 2019 - Lower riskMedical device
Cincinnati Sub-Zero Products LLC, a Gentherm Company recalls MICRO-TEMP LT System, Model 749- Localized Heat Therapy System is intended to warm a patient's body part through
Sub-Zero Products recalls Micro-TEMP LT System Model 749 localized heat therapy devices for potential tissue damage if temperatures exceed 40°C for extended periods.
Sub-Zero ProductsJul 19, 2019 - Lower riskMedical device
Fujifilm Medical Systems U.S.A., Inc. recalls Fujifilm FDR Go Plus mobile X-ray system
Fujifilm recalls FDR Go Plus mobile X-ray systems due to potential Blue Screen of Death errors. Affected units have all serial numbers.
FujifilmJul 19, 2019 - Lower riskMedical device
Boston Scientific Corporation recalls AMS 800 Artificial Urinary Sphincter AMS 800 Belt Cuff, 4.5 cm Part Number: 72400161
Boston Scientific recalls AMS 800 Artificial Urinary Sphincter belt cuffs labeled 4.5 cm but actually 4.0 cm. This mislabeling could cause improper fit and complications. Affected units include specific part numbers and lot numbers.
Boston ScientificJul 19, 2019 - Lower riskMedical device
Integra LifeSciences Corp. recalls Codman ISOCOOL Bipolar Forceps-are indicated for cauterizing, coagulating, grasping, and manipulating tissue during
Integra recalls Codman ISOCOOL Bipolar Forceps model 8145100S with inadequate tip insulation that may cause improper tissue coagulation during surgery.
IntegraJul 19, 2019 - Lower riskMedical device
Philips North America, LLC recalls Philips 5-Lead Set, Disposable, Bedside, AAMI Model # 989803173131 Product Usage: Philips Single-Patient-Use ECG lead
Philips recalls 5-lead bedside ECG leads with model #9898031: Thickness may prevent accurate ECG readings. Affected units from 03/18, 05/18, 06/18 lots.
PhilipsJul 19, 2019 - Lower riskMedical device
Aniara Diagnostica LLC recalls ZYMUTEST HIA MonoStrip, IgG ELISA kit, Model No. RK041A, for in vitro diagnostic use.
Aniara Diagnostica recalls ZYMUTEST HIA MonoStrip IgG ELISA kits (Model RK041A) due to residual crystallization causing negative controls to go out of range. Affected kits sold under specific serial numbers.
Aniara DiagnosticaJul 19, 2019 - Lower riskMedical device
Coltene /Whaledent AG recalls DIATECH, swiss dental instruments, ROUND END TAPER, 856-016-7-F
Coltene Whaledent recalls Diatech Diamond dental burs (model 856-016-7-F) due to inconsistent length in a specific batch. Affected units have lot number J22952.
Coltene /WhaledentJul 19, 2019 - Use cautionMedical device
Stryker Corporation recalls Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Single, REF 3910-500-471, UDI 07613327464818, Sterile R, RX Only
Stryker recalls Omega 4.75mm PEEK Knotless Anchor Systems due to difficulty removing the driver, which may cause screws to pull out and create additional bone injury sites.
StrykerJul 19, 2019
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