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
34,894 found- Use cautionVehicle
FREIGHTLINER CASCADIA (2018) recall — Exterior Lighting
Daimler Trucks North America recalls 2018 Freightliner Cascadia trucks with brake light failure risk. If brake lights don't work, drivers may not signal slowing to other vehicles, increasing crash risk. Owners should contact DTNA for free repairs.
Daimler Trucks North AmericaNov 28, 2017 - Lower riskMedical device
DePuy Orthopaedics, Inc. recalls The GLOBAL UNITE Platform Shoulder System is intended for cemented or uncemented total shoulder or hemi-shoulder
DePuy recalls specific lots of GLOBAL UNITE Platform Shoulder System due to screw inversion during assembly, potentially causing surgical delays. Affected patients should contact DePuy for guidance.
DePuyNov 28, 2017 - Lower riskMedical device
Alere San Diego Inc. DBA Immunalysis Corporation recalls lmmunalysis EDDP Urine Control Set 1 The EDDP Urine Controls (High 125 ng/ml and Low 75 ng/ml) are used as control
Immunalysis recalls EDDP Urine Control Set 1 due to potential inaccurate test results. The High control may produce values below 100 ng/mL when used in clinical analyzers, which could lead to false negative results.
ImmunalysisNov 28, 2017 - Use cautionMedical device
Cook Vascular Inc. recalls Vital-Port Vascular Access System, Subcutaneous, implanted, intravascular infusion port and catheter, IP, IP-S, Product
Cook Vascular recalls Vital-Port Vascular Access Systems with non-coring needles that may cut or dislodge septum material during initial implant. Affected patients should contact for remedy.
Cook VascularNov 28, 2017 - Lower riskMedical device
Stryker Neurovascular recalls Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo Pro18 Microcatheter
Stryker Neurovascular recalls Trevo XP ProVue System kits with mismatched carton sleeve and contents. Affected kits may have incorrect packaging. No immediate action needed as the hazard is cosmetic.
Stryker NeurovascularNov 28, 2017 - Lower riskDrug
EAI-JR286 INC recalls Vertra Elemental Resistance (Octyl Methoxycinnamate 6%, Oxybenzone 5%, Titanium Dioxide 6.3%, Zinc Oxide 9.9%) Sun
Vertra Elemental Resistance sunscreen with specific ingredients and batch numbers was recalled due to manufacturing quality issues affecting product viscosity. Consumers should check their product details and contact Vertra for further instructions.
VertraNov 28, 2017 - UnratedDrug
Teva Pharmaceuticals USA recalls Penicillin V Potassium for Oral Solution, USP, 125 mg (200,000 U) per 5 mL, 100 mL (when mixed) bottle, Rx only,
Teva Pharmaceuticals USA recalls Penicillin V Potassium oral solution due to high impurities. This medication, sold in 100mL bottles, may contain unsafe levels of impurities that could pose health risks. Consumers should contact the manufacturer for details.
TevaNov 28, 2017 - Lower riskFood
JP's Delicacies LLC recalls Holi Aioli, Lemon Basil 12oz bottle
JP's Delicacies LLC recalls Holi Aioli and Lemon Basil 12oz bottles with expiration date 7/18/18 due to not meeting manufacturer standards. Consumers should check lot numbers and expiration dates.
JP's Delic: Holi AioliNov 28, 2017 - Lower riskMedical device
Cincinnati Sub-Zero Products LLC recalls Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR Product Usage: A dual reservoir, water
Cincinnati Sub-Zero recalls Hemotherm 400CE and 400MR models due to potential nontuberculous mycobacteria (NTM) infections from improper cleaning. Updated instructions require enhanced disinfection procedures to reduce infection risk.
Cincinnati Sub-ZeroNov 27, 2017 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Syva¿ EMIT¿ 2000 Theophylline Product Usage: The Syva¿ Emit¿ 2000 Theophylline Assay is a homogeneous enzyme
Siemens Healthcare recalls Syva EMIT 2000 Theophylline Assay lot J1 due to potential increased imprecision when used with Beckman AU Clinical Chemistry System. Affected units may show inaccurate results for controls and patient samples.
Siemens HealthcareNov 27, 2017 - Lower riskMedical device
Ethicon, Inc. recalls DERMABOND" PRINEO" Skin Closure System Product Usage: DERMABOND PRINEO System is intended for topical application only
Ethicon recalls DERMABOND PRINEO Skin Closure System that may fall off if not dried within specified time after application. This could lead to wound reopening. Consumers should check product lot numbers and contact Ethicon for details.
EthiconNov 27, 2017 - Lower riskMedical device
Arrow International Inc recalls ARROWg+ard BLUE PLUS Pressure Injectable Two- Lumen CVC Kit Product Usage: The Arrow¿ CVC is indicated to provide
Arrow recalls some CVC kits for missing lot number and expiration stickers. Check your kit for a sticker with lot number, expiration date, and UDI. Contact Arrow for details.
ArrowNov 27, 2017 - Lower riskMedical device
SPINEART SA recalls TRYPTIK(R) 2 C-PLATE SELF-TAPPING POLYAXIAL SCREW 4.0 MM, LENGTH 14 MM, REF TRY-PS-40 14-S, Qty 2 TRYPTIK(R) 2C-Plate
SPINEART recalls TRYPTIK 2C-Plate screws with batch 3-5934 due to incorrect labeling showing a self-drilling screw sketch. This may cause confusion in surgical use. Affected patients should contact SPINEART for guidance.
SPINEARTNov 27, 2017 - Lower riskFood
H. A. R. Maspeth Corp. recalls WOLDONG WORLD'S BEST KIMCHI WHOLE CABBAGE KIMCHI PREMIUM 3LBS (1.36kg), UPC: 8 46034 04853 9 and 7LBS (3.17kg), UPC:
H. A. R. Maspeth Corp. recalls WOLDONG World's Best Kimchi Premium 3Lb and 7Lb jars due to undeclared sesame seeds. Consumers should check UPCs and contact for details.
WOLDONGNov 27, 2017 - UnratedMedical device
United Orthopedic Corporation recalls U2 Total Knee System Tibial Insert, Posterior Stabilized, #3, 11mm Thick Catalogue number 2303-3032 The U2 Total Knee
United Orthopedic Corporation recalls U2 Total Knee System Tibial Insert due to packaging mismatch with product labeling. Affected units may have incorrect contents.
United Orthopedic CorporationNov 24, 2017 - Use cautionVehicle
BISON TRAIL EXPRESS (2010) recall — Equipment
Bison is recalling 2010 Trail Express trailers with certain Kidde fire extinguishers that may become clogged or detach during a fire, increasing injury risk. Owners should contact Bison or Kidde for a free replacement.
BisonNov 22, 2017 - Use cautionVehicle
CRUISER RV SOUTH FORK (2017) recall — Equipment
Cruiser RV is recalling certain 2017 South Fork RVs with defective Kidde fire extinguishers that may clog or detach, increasing injury risk during fires. Owners must contact Kidde for a free replacement.
Cruiser RVNov 22, 2017 - Use cautionVehicle
THOR MOTOR COACH ACE (2018) recall — Equipment
Thor is recalling 2018 motor coaches with specific fire extinguishers that may not function properly during fires, increasing injury risk. Owners must contact Thor or Kidde for a free replacement.
ThorNov 22, 2017 - Use cautionVehicle
HEARTLAND SUNDANCE XLT TT (2018) recall — Equipment
Heartland is recalling 2018 Sundance XLT TT RVs with certain Kidde fire extinguishers that may become clogged or detach, increasing fire injury risk. Owners must contact Kidde for a free replacement.
HeartlandNov 22, 2017 - Use cautionVehicle
DRV MOBILE SUITE (2018) recall — Equipment
DRV is recalling certain 2018 Mobile Suites with Kidde fire extinguishers that may become clogged or detach during fires, increasing injury risk. Owners should contact DRV or Kidde for a free replacement.
DRVNov 22, 2017 - Use cautionVehicle
CROSSROADS REDWOOD (2018) recall — Equipment
Keystone is recalling 2018 Crossroads RVs with defective fire extinguishers that may clog or detach during a fire, increasing injury risk. Owners must contact Kidde for a free replacement.
KeystoneNov 22, 2017 - Use cautionVehicle
COACHMEN PRISM (2018) recall — Equipment
Forest River is recalling certain 2018 Coachmen Prism motorhomes with Kidde fire extinguishers that may become clogged or detach, increasing injury risk during fires. Owners must contact Kidde for a free replacement.
Forest RiverNov 22, 2017 - UnratedMedical device
Atrium Medical Corporation recalls ProLite Mesh - mesh, surgical, polymeric ProLite Mesh is intended for use in soft tissue deficiencies including hernia
Atrium Medical recalls ProLite Mesh product code 1010306-06 with lot 412298 due to incorrect packaging configuration that may lead to improper use in hernia repairs.
Atrium MedicalNov 22, 2017 - Lower riskMedical device
Apollo Endosurgery Inc recalls Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: The Lap-Band system consists of a silicone band with
Apollo recalls Lap-Band AP System Small with RapidPort EZ due to missing component in package. Affected units include specific lot and serial numbers listed. No action needed as the missing part is not functional.
ApolloNov 22, 2017 - Lower riskMedical device
Medical Components, Inc dba MedComp recalls 8F Plastic Dignity¿ Low Profile CT Port W/Pre-Attached ChronoFlex¿ Polyurethane Catheter
MedComp recalls 8F Plastic Dignity Low Profile CT Port kits with incorrect unmarked guidewires. These kits may cause complications during medical procedures. Affected kits have specific lot numbers and expiration dates.
MedCompNov 22, 2017 - Lower riskMedical device
ECOLAB INC recalls ECOLAB MICROTEK Rolled Probe Cover, 2.6 cm x 20 cm (1 in x 8 in), Ref PC0906, packaged 1 probe cover/pouch, 25
Ecolab recalls 25 pouches of Microtek Rolled Probe Covers due to incorrect instructions shipped. This may lead to improper use in medical procedures. Affected units have specific lot numbers.
EcolabNov 22, 2017 - Lower riskMedical device
Smiths Medical ASD Inc. recalls CADD-Legacy 1, Model 6400 Ambulatory Infusion Pump, REF 21-6400-51, PC 10008552-001, Smiths Medical ASD, Inc. Rx ONLY
Smiths Medical recalls CADD-Legacy 1 Model 6400 infusion pumps with non-matching serial numbers. Affected units may have incorrect serial numbers listed on the pump label versus software. No action is required for these units.
Smiths MedicalNov 22, 2017 - Lower riskFood
Saranac Brand Foods, Inc. recalls Saranac Pasta and Seafood Salad 2x10lbs or 2x5lbs plastic tubs.
Saranac recalls 2x10lb and 2x5lb pasta and seafood salad tubs due to undeclared crab. Consumers should check lot codes on stickers for affected products.
SaranacNov 22, 2017 - Lower riskFood
Colorado Nut Co recalls Frontier Trail Mix (4 oz. bag), UPC 018142352987. Packaged in Plastic Zip Lock bags. No refrigeration needed.
Colorado Nut Co recalls Frontier Trail Mix (4 oz. bags) due to undeclared milk. Products manufactured June 1-2017 through November 7, 2017 with specific lot numbers.
Colorado Nut CoNov 22, 2017 - Stop using nowConsumer product
Goal Zero Recalls Solar Powered Charging Stations Due to Impact Hazard (Recall Alert)
Goal Zero recalls Street Charge solar charging stations due to a weld failure risk. Stop using immediately and contact Goal Zero for a free repair.
Goal ZeroNov 22, 2017
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