The Recall Desk

Archive

July 2018 recalls

502 recalls were announced in July 2018.

What the numbers show

Critical
34
Severe
167
High
225
Moderate
62
Low
14

Of the 502 recalls this month scored against our rubric, 7% are Critical, 33% are Severe.

Which agencies issued them

201–300 of 502

  • SevereFDA (Food)·F-1615-2018·2018-07-18

    Hee Chang Dairy Black Bean Cereal Latte Recalled for Undeclared Allergens

    Hee Chang Dairy & Food Co., LTD is recalling Black Bean Cereal Latte because FDA inspection found undeclared allergens in the product.

    Product
    Black Bean Cereal Latte; 28.2 oz. package Ingredients: Non Dairy Creamer (corn syrup, vegetable oil, Sodium Caseinate, Silicon dioxide), Rice Powder, Bean Powder, Silicon dioxide, Refined Salt, Black Sesame. Corn syrup 57% Hydrogenated coconut oil 28% Sweet whey powder 10%
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1030-2018·2018-07-18

    AuroMedics Recalls Piperacillin and Tazobactam Injection Vials Due to Particulate Matter

    AuroMedics Pharma LLC is recalling 73,620 vials of Piperacillin and Tazobactam for Injection due to the presence of glass and silicone particulate matter.

    Product
    PIPERACILLIN AND TAZOBACTAM — PIPERACILLIN AND TAZOBACTAM (PIPERACILLIN SODIUM AND TAZOBACTAM SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0994-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Elephant, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V478000·2018-07-18

    Freightliner Cascadia Trucks Recalled for Tire Cords Visible Through Innerliner

    Daimler Trucks North America is recalling 2019 Freightliner Cascadia trucks equipped with specific Continental tires because visible cords may cause sudden air loss and loss of vehicle control.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E057000·2018-07-18

    Brembo Recalls Federal Mogul Rear Brake Pads Due to Material Detachment

    Brembo is recalling certain Federal Mogul rear brake pads because the material may detach from the back plate, potentially affecting braking performance.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:DISC:PADS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1613-2018·2018-07-18

    Del Monte Vegetable Tray Recalled for Potential Cyclospora Contamination

    Del Monte is recalling 28 oz. vegetable trays with dip due to a potential link to a recent cluster of illnesses and possible Cyclospora contamination.

    Product
    Del Monte 28 oz. Small Veg Tray w/dip contains baby carrots, broccoli, cauliflower, celery sticks and dill dip
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-2400-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce component strength and lead to premature breakage.

    Product
    Femoral Nail, A/R, R1500 T2 Femur ¿12x360 mm, Product Number 18281236S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2419-2018·2018-07-18

    Medtronic EnTrust ICD Recall for Potential Loss of High Voltage Therapy

    Medtronic is recalling 8,821 EnTrust ICDs due to a potential loss of high voltage therapy near end-of-life. Patients should contact their healthcare provider.

    Product
    Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D154VRC Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular antitachycardia pacing and ventricular def
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2406-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Femoral Nail, RIGHT T2 GTN ¿14x460 mm, Product Number 18511446S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2380-2018·2018-07-18

    Intuitive Surgical Recalls da Vinci Xi Stapler Reloads Due to Missing Component

    Intuitive Surgical is recalling da Vinci Xi Stapler 45 Reloads because a missing knife mechanism component may prevent the device from cutting tissue.

    Product
    da Vinci Xi EndoWrist Stapler 45 Reload Blue, Model 48645B-03, 12 reloads/box.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2418-2018·2018-07-18

    Medtronic EnTrust ICD Recall for Potential Loss of High Voltage Therapy

    Medtronic is recalling 3 EnTrust ICDs because they may lose high voltage therapy near battery end-of-life without prior warning.

    Product
    Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D153VRC Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular antitachycardia pacing and ventricular def
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2404-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Femoral Nail, LEFT T2 GTN ¿14x300 mm, Product Number 18501430S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2405-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce component strength and lead to premature breakage.

    Product
    Femoral Nail, RIGHT T2 GTN ¿9x320 mm, Product Number 18510932S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2398-2018·2018-07-18

    Stryker Recalls Seven Femoral Nails Due to Potential Breakage Risk

    Stryker GmbH is recalling seven femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Femoral Nail, A/R, R1500 T2 Femur ¿10x320 mm, Product Number 18281032S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2407-2018·2018-07-18

    Stryker Recalls Ankle Arthrodesis Nails Due to Potential Breakage Risk

    Stryker GmbH is recalling specific ankle arthrodesis nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Ankle Arthrodesis Nail, right T2 Ankle ¿10x300mm, Product Number 18191030S
    Category
    Medical Device
    Distribution
    8 states
  • SevereNHTSA·18V479000·2018-07-18

    Freightliner Recalls 2019 Cascadia Trucks for Tire Defect

    Daimler Trucks North America is recalling 2019 Freightliner Cascadia trucks equipped with specific Continental tires that may lose air suddenly, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2394-2018·2018-07-18

    Stryker Recalls Two Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling two femoral nails that may have non-conforming cannulation, potentially leading to reduced strength and premature breakage.

    Product
    Femoral Nail, A/R T2 Femur ¿10x320 mm, Product Number 18251032S
    Category
    Medical Device
    Distribution
    8 states
  • SevereNHTSA·18V475000·2018-07-18

    Forest River Recalls 2018-2019 Trailers Due to Wheel Bearing Defect

    Forest River is recalling 2018-2019 Rockwood and Flagstaff trailers because inner wheel bearings may seize, causing wheels to lock up and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2397-2018·2018-07-18

    Stryker Recalls Specific Femoral Nail Due to Potential Breakage Risk

    Stryker GmbH is recalling specific femoral nails due to potential manufacturing defects that could cause the device to break prematurely.

    Product
    Femoral Nail, A/R T2 Femur ¿15x240 mm, Product Number 18251524S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2417-2018·2018-07-18

    Medtronic EnTrust ICD Recall for Potential Loss of High Voltage Therapy

    Medtronic is recalling 8,890 EnTrust ICDs due to a potential loss of high voltage therapy near end-of-life. Patients should contact their healthcare provider.

    Product
    Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D154ATG Product Usage: The device indicated for use in ICD patients with atrial tachyarrhythmias, or who are at significant risk of developing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2393-2018·2018-07-18

    Stryker Tibial Nail Recall Due to Potential Premature Breakage

    Stryker GmbH is recalling specific Tibial Nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Tibial Nail, Standard T2 Tibia ¿12x315 mm, Product Number 18221231S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2401-2018·2018-07-18

    Stryker Recalls Specific Femoral Nail Products Due to Potential Breakage

    Stryker GmbH is recalling specific femoral nails due to potential manufacturing defects that could cause the device to break prematurely.

    Product
    Femoral Nail, A/R, R1500 T2 Femur ¿12x380 mm, Product Number 18281238S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Food)·F-1612-2018·2018-07-18

    Del Monte Vegetable Trays Recalled for Potential Cyclospora Contamination

    Del Monte is recalling 6 oz. and 12 oz. vegetable trays with dip due to a potential link to a recent cluster of illnesses and possible Cyclospora contamination.

    Product
    Del Monte 6 oz. Veg Tray w/dip; Del Monte 12 oz. Veg Tray w/dip contains baby carrots, broccoli, cauliflower and dill dip
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-1619-2018·2018-07-18

    Brew Dr. Kombucha Recalled Due to Glass Fragments in Bottles

    Brew Dr. Kombucha is recalling Clear Mind kombucha bottles because glass fragments were found inside. Consumers should stop using the affected products.

    Product
    Brew Dr. Kombucha Clear Mind, item Code: FCG0002, 6 glass bottles per case, net volume: 32 FL OZ (946 ML). UPC: 51107 00369. The bottle's label is read in parts: "***CLEAR MIND***INGREDIENTS: Brewed tea (filtered water, organic green tea, organic rosemary, organic peppermint,
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-2408-2018·2018-07-18

    Stryker Recalls Ankle Arthrodesis Nails Due to Potential Breakage Risk

    Stryker GmbH is recalling specific ankle arthrodesis nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Ankle Arthrodesis Nail, right T2 Ankle ¿11x300mm, Product Number 18191130S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2395-2018·2018-07-18

    Stryker Recalls 17 Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling 17 femoral nails because non-conforming cannulation may reduce component strength and cause premature breakage.

    Product
    Femoral Nail, A/R T2 Femur ¿10x340 mm, Product Number 18251034S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2403-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Femoral Nail, LEFT T2 GTN ¿12x360 mm, Product Number 18501236S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2420-2018·2018-07-18

    Medtronic EnTrust Escudo ICD Recall for Potential Loss of Therapy

    Medtronic is recalling EnTrust Escudo ICDs due to a potential loss of high voltage and anti-tachycardia pacing therapy as the battery nears its end of life.

    Product
    Medtronic EnTrust Escudo D144VRC (OUS distribution) Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular antitachycardia pacing and ventricular defibrillation for automated treatment of life-threatening ventricular arrhythmias.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2415-2018·2018-07-18

    Medtronic Percepta CRT-P MRI SureScan Devices Recalled for Potential Reset

    Medtronic is recalling Percepta CRT-P MRI SureScan devices due to a potential device reset caused by a timing interaction between specific diagnostic and pacing features.

    Product
    Percepta Quad CRT-P MRI SureScan, REF W4TR04 Product Usage: The CRT-P models are implantable pulse generators with cardiac resynchronization therapy (CRT-P). These devices monitor and regulate the patient s heart rate by providing single or dual chamber rate responsive bradyc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1611-2018·2018-07-18

    FDA Recalls Frozen Tilapia Fillets Due to Listeria Monocytogenes Contamination

    R F A Inc. is recalling frozen natural tilapia fillets packed for Osamu Corporation due to potential Listeria monocytogenes contamination.

    Product
    Frozen Natural Tilapia + Belly V-Pack, Farm Raised Tilapia, Product of Costa Rica, Packed for Osamu Corporation Carson, California 90810
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2416-2018·2018-07-18

    Medtronic EnTrust ICD Recall for Potential Loss of High Voltage Therapy

    Medtronic is recalling 103 EnTrust Dual Chamber ICDs because they may lose high voltage and anti-tachycardia pacing therapy near end-of-life without prior warning.

    Product
    Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D153ATG Product Usage: The device indicated for use in ICD patients with atrial tachyarrhythmias, or who are at significant risk of developing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2396-2018·2018-07-18

    Stryker Recalls Nine Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling nine femoral nails because non-conforming cannulation may reduce component strength and cause premature breakage.

    Product
    Femoral Nail, A/R T2 Femur ¿12x360 mm, Product Number 18251236S
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-2381-2018·2018-07-18

    Intuitive Surgical Recalls da Vinci Xi Stapler Reloads Due to Missing Component

    Intuitive Surgical is recalling da Vinci Xi Stapler 45 Reloads because a missing knife mechanism component may prevent the device from cutting tissue during surgery.

    Product
    da Vinci Xi EndoWrist Stapler 45 Reload Green, Model 48445G-03, 12 reloads/box.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·18V474000·2018-07-18

    Micro Bird Recalls School Buses for Seat Foam Crash Protection Defect

    Micro Bird is recalling 2011-2018 school buses because seat foam may not absorb enough impact in a crash, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES SCHOOL BUS, G5 SCHOOL BUS, MB II SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2414-2018·2018-07-18

    Medtronic Percepta CRT-P MRI SureScan Recall for Device Reset Risk

    Medtronic is recalling 1,604 Percepta CRT-P MRI SureScan implantable pulse generators due to a potential device reset caused by a timing interaction between diagnostic and pacing features.

    Product
    Percepta CRT-P MRI SureScan, REF W1TR04 Product Usage: The CRT-P models are implantable pulse generators with cardiac resynchronization therapy (CRT-P). These devices monitor and regulate the patient s heart rate by providing single or dual chamber rate responsive bradycardia
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2424-2018·2018-07-18

    Proteus 235 Proton Beam Device Recalled for Correction Vector Loss

    Ion Beam Applications S.A. is recalling three Proteus 235 units because a software defect may cause patients to be treated in the wrong position.

    Product
    Proteus 235, Version PTS-11.0.1.2 and PTS-11.0.2 Product Usage: A device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2378-2018·2018-07-18

    Medline Recalls Bard MYPICC Kits Due to Potential Sterilization Failure

    Medline Industries is recalling specific Bard MYPICC Kits because one case may not have been sterilized. The product was distributed to UT.

    Product
    BARD MYPICC Kit, REF CK000095B, 5F French Size, packaged 5 kits/case, Sterile, RX, For use in vascular access procedures.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Drugs)·D-1011-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling White Borneo Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, White Borneo, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2422-2018·2018-07-18

    Cayenne Medical Recalls AperFix AM Femoral Implants Due to Breakage Risk

    Cayenne Medical Inc. is recalling 976 units of AperFix AM Femoral Implants because they may break inside the femoral socket during orthopedic use.

    Product
    AperFix AM Femoral Implant, Model numbers CM-2409 (9mm x 24 mm) and CM-2410 (10 mm x 24 mm). For orthopedic use in ligament reconstruction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1617-2018·2018-07-18

    Citron Tea Recalled for Undeclared Allergens in Citron Powder

    Hee Chang Dairy & Food Co. is recalling Citron Tea packets because the citron powder contains undeclared corn syrup and lactose.

    Product
    Citron Tea; 35.3 oz. (1 kg) packet Ingredients: White Sugar, Dried Citron Powder, Citric Acid, carboxymethylcellulose, Sodium citrate; Silicon dioxide, Citron Flavor. Citron Powder contains corn syrup 58% and Lactose 20% Imported and Distributed by: Coffee Tree USA 2
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2429-2018·2018-07-18

    bioMerieux Recalls VIDAS Analyzers and Quality Control Tests for Performance Issues

    bioMerieux is recalling VIDAS analyzers and Quality Control VIDAS tests due to pump clogging and label displacement that may cause erroneous assay results.

    Product
    BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usage: the Quality Control VIDAS (QCV) is an automated test for use on the VIDAS¿ system to detect abnormal operation of the VIDAS and mini VIDAS instrument pipette mechanisms and optical system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1014-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling White Thai Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, White Thai, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2389-2018·2018-07-18

    Roche Vitamin D Test System Recalled for Falsely Elevated Results

    Roche Diagnostics is recalling the Elecsys Vitamin D total II test system because it may produce falsely elevated, non-reproducible results, potentially leading to incorrect vitamin D dosage adjustments.

    Product
    Elecsys Vitamin D total II, Vitamin D Test System, Material number 07028148190 Product Usage: This assay is intended for the quantitative determination of total 25-hydroxyvitamin D in human serum and plasma. This assay is to be used as an aid in the assessment of vitamin D su
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2412-2018·2018-07-18

    Medtronic Percepta CRT-P MRI SureScan Recall for Device Reset Risk

    Medtronic is recalling 1,842 Percepta CRT-P MRI SureScan implantable pulse generators due to a potential device reset caused by a timing interaction between diagnostic and pacing features.

    Product
    Percepta CRT-P MRI SureScan, REF W1TR01 Product Usage: The CRT-P models are implantable pulse generators with cardiac resynchronization therapy (CRT-P). These devices monitor and regulate the patient s heart rate by providing single or dual chamber rate responsive bradycardia
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1616-2018·2018-07-18

    Black Bean Job's Tears Tea Recalled for Undeclared Allergens

    Hee Chang Dairy & Food Co., LTD is recalling Black Bean Job's Tears Tea because FDA inspection found undeclared allergens in the product.

    Product
    Black Bean Job's Tears Tea, 35.3 oz. (KG) package Ingredients: Non Dairy Creamer (corn syrup, Palm oil, Lactose, Whey Powder, Dipotassium Phosphate, Silicon dioxide, Refined Salt, Milk flavor), citron Syrup, Rice, Job's Tears Corn, Black Bean Powder, guar gum. The non-dai
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2390-2018·2018-07-18

    Roche Vitamin D Test System Recalled for Falsely Elevated Results

    Roche Diagnostics is recalling the Elecsys Vitamin D total II test system because it may produce falsely elevated and non-reproducible results, potentially leading to incorrect vitamin D dosage adjustments.

    Product
    Elecsys Vitamin D total II, Vitamin D Test System, Material number 07464215160 Product Usage: This assay is intended for the quantitative determination of total 25-hydroxyvitamin D in human serum and plasma. This assay is to be used as an aid in the assessment of vitamin D su
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2421-2018·2018-07-18

    Medtronic EnTrust Escudo ICD Recall for Potential Loss of Therapy

    Medtronic is recalling 1,867 EnTrust Escudo ICDs because they may lose high-voltage therapy without a prior alert.

    Product
    Medtronic EnTrust Escudo D144DRG (OUS distribution) Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular antitachycardia pacing and ventricular defibrillation for automated treatment of life-threatening ventricular arrhythmias.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2386-2018·2018-07-18

    GE Medical Systems Recalls Discovery IGS 730 X-ray Systems

    GE Medical Systems is recalling 102 Discovery IGS 730 Interventional Fluoroscopic X-ray Systems due to potential X-ray abort errors that may cause loss of imaging mode.

    Product
    Discovery IGS 730 Interventional Fluoroscopic X-ray Systems
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Food)·F-1618-2018·2018-07-18

    Green Tea Latte Recalled for Undeclared Allergens

    Hee Chang Dairy & Food Co., LTD is recalling Green Tea Latte packets because an FDA inspection found undeclared allergens in the product.

    Product
    Green Tea Latte; 35.3 oz. (1 kg) packet Ingredients: White sugar, Instant Whole Milk Powder (Corn Syrup, Milk cream, Lactose, Lecithin, Sodium Caseinate, Non Dairy Creamer (corn Syrup, vegetable oil, sodium caseinate, Silicon Dioxide, Skim Milk Powder, Whey Powder, Green Tea P
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-1015-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Yellow Thai, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2409-2018·2018-07-18

    Immuno-Mycologics Recalls Cryptococcal Antigen Lateral Flow Assay Strips

    Immuno-Mycologics is recalling 875 units of Cryptococcal Antigen Lateral Flow Assay strips due to a defect that may cause false negative test results.

    Product
    Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Model # CR2003 Product Usage: The CrAg Lateral Flow Assay is an immunochromatographic test system for the qualitative or semi-quantitative detection of the capsular polysaccharide antigens of Cryptococcus species complex (Cry
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2426-2018·2018-07-18

    Stryker Recalls Reprocessed Coronary Sinus Diagnostic Catheters

    Stryker Sustainability Solutions is recalling 2,722 reprocessed Coronary Sinus Diagnostic EP Catheters because thrombogenicity tests showed they did not meet non-thrombogenic specifications.

    Product
    Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP) Catheter, catalog numbers D135303 and D135304. Product Usage: The Reprocessed CS Diagnostic EP Catheter is indicated for electrophysiological mapping of cardiac structures; i.e., stimulation and recording o
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0916-2018·2018-07-18

    Akorn Recalls Acetylcysteine for Injection Due to Manufacturing Deviations

    Akorn, Inc. is recalling 89,507 vials of Acetylcysteine for Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall is classified as FDA Class II.

    Product
    Acetylcysteine for Injection 6 g/30 mL (200 mg/mL). Rx Only. Manufactured by Akron Inc., Lake Forest, IL 60045. NDC 17478-660-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2402-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce component strength and cause premature breakage.

    Product
    Femoral Nail, LEFT T2 GTN ¿10x360 mm, Product Number 18501036S
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-2391-2018·2018-07-18

    Ekla Recalls NOVAPLUS Pregnancy Test Kits Due to Incorrect Results

    Ekla Corporation is recalling 295 NOVAPLUS Pregnancy Cassette Devices because they may provide incorrect hCG results. The affected kits were distributed in California, Illinois, Minnesota, and Rhode Island.

    Product
    NOVAPLUS(R) Pregnancy Cassette Device with Droppers, Urine hCG Pregnancy Cassette, Cat. No. VPT1-CASS Product Usage: pregnancy test
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-2427-2018·2018-07-18

    FDA Recalls LigaSure Exact Dissector Nano Coated Due to Sterile Breach

    FDA is recalling 936 units of LigaSure Exact Dissector Nano Coated instruments because sterile pouches were found with punctures.

    Product
    LigaSure" Exact Dissector Nano Coated 20.6mm-21cm Product Usage: A bipolar electrosurgical instrument intended for use in open surgical procedures where ligation and division of vessels, tissue bundles, and lymphatics is desired.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2411-2018·2018-07-18

    Fort Defiance P2131 Steam Sterilizer Recalled for Plumbing Deposits

    Fort Defiance Industries is recalling 199 P2131 Automated Field Steam Sterilizers because stagnant water and metal interactions can create deposits that interfere with the rear sight gauge or water liquid level switch.

    Product
    FDI FORT DEFIANCE INDUSTRIES P2131 AUTOMATED FIELD STEAM STERILIZER, NSN: 6530-01-641-4641 Product Usage: The Fort Defiance Industries Automated Field Steam Sterilizer Model P2131 is designed for sterilization of porous and non-porous, heat- and moisture-stable materials (e.g
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1620-2018·2018-07-18

    Earthrise Natural Spirulina Recalled for Potential Metal Contamination

    Earthrise Nutritionals is recalling 1,014 boxes of Natural Spirulina because the product may contain small metal pieces from a sifter screen.

    Product
    Earthrise Natural Spirulina; Net Weight: 20.0 kg( 44.0 lbs); Double bag sealed - 1 bag per box. UPC: 0 32602 99040 3
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2413-2018·2018-07-18

    Medtronic Percepta CRT-P MRI SureScan Devices Recalled for Potential Reset

    Medtronic is recalling Percepta CRT-P MRI SureScan devices due to a timing interaction that may cause a device reset.

    Product
    Percepta Quad CRT-P MRI SureScan, REF W4TR01 Product Usage: The CRT-P models are implantable pulse generators with cardiac resynchronization therapy (CRT-P). These devices monitor and regulate the patient s heart rate by providing single or dual chamber rate responsive bradyc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2392-2018·2018-07-18

    Steris Reliance 1227 Washer/Disinfector Recalled for Chemical Alarm Failure

    Steris is recalling Reliance 1227 Washer/Disinfector units because the low chemical level alarm does not operate as intended, potentially preventing proper cleaning of patient care items.

    Product
    Reliance 1227 Cart and Utensil Washer/Disinfector, FW03101, FW03102, FW03S003 Product Usage: The Reliance 1227 Cart and Utensil Washer/Disinfector is intended for use in the cleaning and low-level disinfection of bedpans and urinals, basins, carts, beds, theatre shoes and oth
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2379-2018·2018-07-18

    Smiths Medical Recalls BCI Advisor Vital Signs Monitors Due to Printing Defects

    Smiths Medical ASD Inc. is recalling 10 BCI Advisor Vital Signs Monitors because certain printing modes may not function properly.

    Product
    BCI Advisor Vital Signs Monitor, Model 9200, Reorder numbers 920654235, 920654235, 920654335A, and 920674235A. (The differences in the reorder numbers have to do with certain functions being installed or not installed.) Product Usage: The 9200 vital signs monitor is intended
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1614-2018·2018-07-18

    Blue Bell Vanilla Ice Cream Cups Recalled for Missing Allergen Labeling

    Blue Bell Creameries is recalling 136 boxes of 3-ounce vanilla ice cream cups because they were distributed for retail sale without required nutrition and allergen labels.

    Product
    Blue Bell Ice Cream, Brand Homemade Vanilla Flavored, 3 FL OZ (88 mL), Cups, 24 per box, This Unit Not Labeled For Retail Sale
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Drugs)·D-0918-2018·2018-07-18

    SCA Pharmaceuticals Recalls Subpotent Buffered Lidocaine Injection

    SCA Pharmaceuticals is recalling 3,984 syringes of Buffered Lidocaine 1% Injection because stability data does not support the current expiration dating.

    Product
    Buffered Lidocaine 1% with Sodium Bicarbonate Injection for Local Anesthetic Use (Concentration=10 mg/mL) 0.25 mL Total Volume, Rx only , SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205 877-550-5059
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0917-2018·2018-07-18

    Medgyn Recalls Monsel's Solution for Manufacturing Practice Deviations

    Medgyn Products, Inc. is recalling 2,750 boxes of Monsel's Solution because the product was not manufactured under current good manufacturing practices.

    Product
    Monsel's Solution (Ferric Subsulfate), 20%, packaged as 12 single application vials and 12 applicators, 8 mL per box, Manufactured For: MedGyn Products, Inc., 100 W. Industrial Rd., Addison, IL 60101 USA; Manufactured By: BioDiagnostics Intl, 555 West Lambert Road Unit-C, Brea, C
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0912-2018·2018-07-18

    Wockhardt Recalls Enalapril Maleate Tablets Due to Impurity Failures

    Wockhardt Limited is recalling specific batches of Enalapril Maleate Tablets USP because they failed impurity and degradation specifications.

    Product
    Enalapril Maleate Tablets USP; 5 mg NDC code 64679-924-03. 1000 Tablets HDPE container pack with Non CRC cap and 2 desiccants further packed in E-flute cartons.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0925-2018·2018-07-18

    Sanofi Recalls Admelog Insulin Pens Due to Temperature Abuse

    Sanofi-Aventis is recalling 3,214 Admelog insulin pens because they may not have been shipped at the proper temperature.

    Product
    ADMELOG — ADMELOG (INSULIN LISPRO)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0919-2018·2018-07-18

    Medi-Fare Recalls Potassium Chloride Syringes Due to Fill Volume Error

    Medi-Fare Drug and Home Health Center is recalling 1,116 syringes of Potassium Chloride For Injection Concentrate because they were filled with 19 mL instead of the labeled 20 mL.

    Product
    Potassium Chloride For Injection Concentrate syringe 40 mEq/20 mL (2 mEq/mL), Rx only, Medi-Fare Drug Pharmaceutical Compounding 300 West Pine St., Blacksburg, SC 29702 800-622-0007
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2387-2018·2018-07-18

    GE Medical Systems Recalls Innova IGS Fluoroscopic X-ray Systems

    GE Medical Systems is recalling 102 Innova IGS fluoroscopic X-ray systems due to a defect that may cause X-ray abort errors, resulting in the loss of imaging mode during use.

    Product
    Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems
    Category
    Medical Device
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-2423-2018·2018-07-18

    Anika Hyalomatrix Wound Dressings Recalled for Packaging Degradation

    Anika Therapeutics is recalling Hyalomatrix wound dressings because PVC in the packaging degraded during sterilization, potentially compromising product integrity.

    Product
    Hyalomatrix, Product nos. 651105, 651103, 651104, and 651301 Product Usage: Hyalomatrix is a bi-layered, sterile, flexible, and comfortable wound dressing that acts as an advanced wound care device. It is comprised of a non-woven pad entirely composed of HY AFF 11, a benzyl e
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2385-2018·2018-07-18

    Arrow International Recalls Midline Catheter Kits Due to Labeling Issues

    Arrow International is recalling 2,070 Peripherally Inserted Midline Catheter Kits because the product pouch label may not easily identify the lot number, expiration date, and associated symbols.

    Product
    Peripherally Inserted Midline Catheter Kit with Placement Wire, REF MK-02031-TW Product Usage: To provide real time tip location information of a central venous catheter by utilization of ECG to observe P-wave changes as the tip approaches the right atrium of the heart via th
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2388-2018·2018-07-18

    GE Medical Systems Recalls Discovery IGS 740 X-ray Systems

    GE Medical Systems is recalling 102 Discovery IGS 740 systems because X-ray abort errors may cause loss of imaging mode during fluoroscopic use.

    Product
    Discovery IGS 740 Interventional Fluoroscopic X-ray Systems
    Category
    Medical Device
    Distribution
    16 states
  • ModerateFDA (Food)·F-1622-2018·2018-07-18

    Sparkling ICE Cherry Limeade Recalled for Off-Taste and Off-Odor Complaints

    Talking Rain Beverage Co Inc is recalling Sparkling ICE Cherry Limeade after customer complaints reported off-taste and off-odor.

    Product
    Sparkling ICE Cherry Limeade Naturally Flavored Sparking Water, packaged in a PET bottles with a plastic cap, Net Wt. 17 ounces (502.8 ml). UPC code on bottle: 0 16571 95084 2. UPC on Single Pack Wrapper (1 flavor/12 bottles): 016571953126 UPC on Single Pack Wrapper (1 flavo
    Category
    Food
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-2410-2018·2018-07-18

    Ohio Medical Vacuum Regulator Recalled for Incomplete Quality Control Testing

    Ohio Medical Corporation is recalling 11 Vacuum Regulator units because final quality control testing was not completed before distribution.

    Product
    Vacuum Regulator, Push-T-Set Intermittent Suction Unit (PTS-ISU) Product Usage: The vacuum regulator is intended to be used in a medical facility as a means to evacuate media (i.e. fluids) from the body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2383-2018·2018-07-18

    Arrow International Recalls VPS Rhythm ECG Accessory Packs Due to Labeling Issues

    Arrow International is recalling 2,070 VPS Rhythm ECG Accessory Packs because the product pouch label may not easily identify the lot number, expiration date, and associated symbols.

    Product
    VPS Rhythm ECG Accessory Pack, REF RHY-100-ECGO Product Usage: To provide real time tip location information of a central venous catheter by utilization of ECG to observe P-wave changes as the tip approaches the right atrium of the heart via the Superior Vena Cava (SVC). The
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2382-2018·2018-07-18

    Arrow International Recalls VPS Rhythm ECG Accessory Packs for Labeling Issues

    Arrow International Inc. is recalling 2,070 units of VPS Rhythm ECG Accessory Packs because the product pouch label may not easily identify the lot number, expiration date, and associated symbols.

    Product
    VPS Rhythm ECG Accessory Pack with Johans Adapter, REF RHY-100-ECGJ Product Usage: To provide real time tip location information of a central venous catheter by utilization of ECG to observe P-wave changes as the tip approaches the right atrium of the heart via the Superior V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2425-2018·2018-07-18

    Dako PD-L1 IHC 22C3 pharmDx Recall for Storage Time Correction

    Dako North America Inc. is recalling 1,051 PD-L1 IHC 22C3 pharmDx kits to correct instructions for use regarding storage time for specific tissue sections.

    Product
    PD-L1 IHC 22C3 pharmDx is a companion diagnostic used to determine PD-L1 levels for determination of patient treatment options.
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Drugs)·D-0927-2018·2018-07-18

    Lupin Recalls Nitrofurantoin Oral Suspension Due to Subpotent Drug

    Lupin Pharmaceuticals is recalling Nitrofurantoin Oral Suspension because the drug is subpotent and failed content uniformity testing.

    Product
    NITROFURANTOIN — NITROFURANTOIN (NITROFURANTOIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2428-2018·2018-07-18

    bioMerieux Recalls mini VIDAS Systems Due to Performance Issues

    bioMerieux is recalling 1,866 mini VIDAS systems because pump clogging and label displacement may cause erroneous test results.

    Product
    BioMerieux mini VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usage: the Quality Control VIDAS (QCV) is an automated test for use on the VIDAS¿ system to detect abnormal operation of the VIDAS and mini VIDAS instrument pipette mechanisms and optical s
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0915-2018·2018-07-18

    American Health Packaging Recalls Enalapril Maleate Tablets Due to Impurities

    American Health Packaging is recalling specific lots of Enalapril Maleate Tablets USP, 5 mg, due to out-of-specification results for a degradation product.

    Product
    Enalapril Maleate Tablets USP, 5 mg, 100 Tablets (10X10) blister cards, 12 cartons in a shipper, Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- NDC 68084-390-01 Carton [68084-390-11 - Unit Dose]
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Devices)·Z-2384-2018·2018-07-18

    Arrow International Recalls VPS TipTracker Stylet Accessory Due to Labeling Issues

    Arrow International Inc. is recalling 2,070 units of the VPS TipTracker Stylet Accessory because the product pouch label may not easily identify the lot number, expiration date, and associated symbols.

    Product
    VPS TipTracker Stylet Accessory, REF RHY-177-TTSAP Product Usage: To provide real time tip location information of a central venous catheter by utilization of ECG to observe P-wave changes as the tip approaches the right atrium of the heart via the Superior Vena Cava (SVC). T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0913-2018·2018-07-18

    Wockhardt Recalls Enalapril Maleate Tablets Due to Impurity Failures

    Wockhardt Limited is recalling specific batches of Enalapril Maleate Tablets USP because they failed impurity and degradation specifications.

    Product
    Enalapril Maleate Tablets USP; 2.5 mg NDC code 64679-923-03. 1000 Tablets HDPE container pack with Non CRC cap and 2 desiccants further packed in E-flute cartons.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0978-2018·2018-07-18

    Mylan Recalls Subpotent Triamterene and Hydrochlorothiazide Tablets Nationwide

    Mylan Pharmaceuticals is voluntarily recalling 28,436 bottles of Triamterene and Hydrochlorothiazide Tablets because the medication was found to be subpotent.

    Product
    Triamterene and Hydrochlorothiazide Tablets, USP 37.5 mg/25 mg, 100-count bottle, Rx only, Mylan Pharmaceuticals, Inc. Morgantown, WV 26505, NDC 0378-1352-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·063-2018·2018-07-17

    Smithfield Recalls Pepperoni Five Cheese Calzones Due to Plastic Contamination

    Smithfield Packaged Meats is recalling approximately 24,048 pounds of pepperoni five cheese calzones that may contain hard, sharp, clear plastic pieces.

    Product
    Smithfield Packaged Meats Corp. — Smithfield Packaged Meats Corp. Recalls Pepperoni Five Cheese Calzone Products Due to Possible Extraneous Material Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E055000·2018-07-17

    Martinrea Brake Hose Recall for Corrosion-Related Fluid Leak Risk

    Martinrea is recalling brake hose assemblies for Chrysler and Ford vehicles that may lack anti-corrosion plating, posing a risk of brake fluid leaks and reduced braking effectiveness.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V473000·2018-07-17

    BMW Recalls 2018 M5 Vehicles Due to Fuel Level Sensor Defect

    BMW is recalling 2018 M5 vehicles because a fuel level sensor may stick to a fuel line, causing inaccurate fuel gauge readings that could lead to stalling and increased crash risk.

    Product
    BMW — BMW M5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·062-2018·2018-07-16

    New Seasons Market Recalls Sesame Noodle Chicken Salad for Undeclared Peanuts

    New Seasons Market is recalling ready-to-eat sesame noodle chicken salad products because they contain peanuts, a major allergen, that are not declared on the label.

    Product
    New Seasons Market Recalls Ready-To-Eat Sesame Noodle Chicken Salad Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·18E054000·2018-07-16

    TRW Brake Caliper Piston Coating Defect Recall for Multiple Vehicle Brands

    TRW is recalling brake caliper pistons with insufficient coating for vehicles from Volkswagen, Fiat Chrysler, BMW, and Mercedes-Benz to prevent reduced braking performance.

    Product
    SERVICE BRAKES, HYDRAULIC recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V470000·2018-07-16

    Ford Recalls 2018 F53 Chassis Due to Wheel Stud Defect

    Ford is recalling 2018 F53 stripped chassis vehicles because improperly heat-treated front wheel studs may break, increasing crash risk.

    Product
    FORD — FORD F53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·061-2018·2018-07-14

    Beautiful Pig Recalls Uninspected Pork and Beef Products

    The Beautiful Pig, Inc. is recalling ready-to-eat and raw pork and beef products produced without USDA inspection. The products were distributed in Oregon and Washington.

    Product
    The Beautiful Pig, Inc. Recalls Ready-To-Eat And Raw Pork And Beef Products Produced Without The Benefit Of Inspection And Shipped Under U.S. Retention
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·18V467000·2018-07-13

    Volkswagen Recalls 2018 Tiguan Vehicles Due to Sunroof Fire Risk

    Volkswagen is recalling 2018 Tiguan vehicles because the panoramic sunroof LED module may short circuit, increasing the risk of a fire.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·18V468000·2018-07-13

    Forest River Recalls 2019 Palomino Campers Due to Incorrect Weight Label

    Forest River is recalling 2019 Palomino hardside truck campers because the Federal Placard lists an incorrect dry weight, which may result in the vehicle being overloaded.

    Product
    FOREST RIVER — FOREST RIVER PALOMINO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E053000·2018-07-12

    Chrysler and Dodge Vehicles Recalled for Cruise Control Defect

    Chrysler is recalling specific 2014-2018 Chrysler 300, Dodge Charger, and Challenger vehicles because a defect may prevent the cruise control system from disengaging.

    Product
    CHRYSLER — CHRYSLER, DODGE 300, CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V466000·2018-07-12

    Multiquip Recalls 2018 Trailers Due to Center-Mounted Jack Collapse Risk

    Multiquip is recalling 2018 TRLR45H and TRLR70USH trailers because the center-mounted jack may collapse under excessive load, increasing the risk of injury.

    Product
    MULTIQUIP — MULTIQUIP TRLR45H, TRLR70USH
    Category
    Vehicle
    Distribution
    Distributed nationwide

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