The Recall Desk

Archive

May 2020 recalls

456 recalls were announced in May 2020.

What the numbers show

Critical
3
Severe
95
High
244
Moderate
97
Low
17

Of the 456 recalls this month scored against our rubric, 1% are Critical, 21% are Severe.

Which agencies issued them

401–456 of 456

  • HighFDA (Devices)·Z-1811-2020·2020-05-06

    Welch Allyn ELI PC Service Recalled for Defibrillation Safety Non-Compliance

    Welch Allyn is recalling ELI PC Service software because it may not meet defibrillation withstand safety requirements for medical electrical equipment.

    Product
    ELI PC. The ELI PC Service automatically converts resting ECG recordings collected with WAM PC patient cables and WebUpload into DICOM 12-lead ECG Waveform files.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1822-2020·2020-05-06

    Avanos Medical Recalls CORFLO PEG Kits Due to Potential Adapter Occlusion

    Avanos Medical is recalling CORFLO Percutaneous Endoscopic Gastrostomy (PEG) Kits because the tube may become blocked at the adapter, potentially delaying or aborting procedures.

    Product
    CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1815-2020·2020-05-06

    Welch Allyn S4 Wireless Telemeter Recall for Defibrillation Safety

    Welch Allyn is recalling S4 Wireless Telemeters and patient cables because they may not meet defibrillation withstand safety standards.

    Product
    S4 and patient cable for the S4 Wireless Telemeter with the following device names: CABLE 10 WIRE LF ECG SNAP ENDS AHA GRAY, CABLE 10 WIRE LF ECG SNAP ENDS IEC GRAY, CBL 10WIRE LF LRG ECG SNAP ENDS AHA GRAY, CBL 10WIRE LF LRG ECG SNAP ENDS IEC GRAY. The S4 mobile monitor prov
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1710-2020·2020-05-06

    GE Healthcare Recalls Lunar iDXA Advance Bone Densitometers Due to Radiation Risk

    GE Healthcare is recalling 123 Lunar iDXA Advance bone densitometers because a control panel issue may cause the start button to stick, potentially leading to accidental radiation exposure.

    Product
    Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1826-2020·2020-05-06

    Elekta Recalls Leksell Vantage Stereotactic System Instrument Carriers

    Elekta Inc is recalling 25 Leksell Vantage Stereotactic System Instrument Carriers because a faulty locking piece may not meet required locking force standards.

    Product
    Leksell Vantage Stereotactic System. Instrument Carrier, Part of Leksell Vantage Arc (1053958). Neurological stereotaxic Instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1810-2020·2020-05-06

    Welch Allyn Electrocardiographs Recalled for Defibrillation Safety Non-Compliance

    Welch Allyn is recalling 78,521 lead diagnostic electrocardiographs because they may not meet defibrillation withstand requirements.

    Product
    Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI 150c, ELI 250c, ELI 230, ELI 280, ELI 380, R-Scribe and Connex Cardio. Product Usage: A non-invasive prescription device indicated for use to acquire, analyze, display, transmit and pri
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1812-2020·2020-05-06

    Welch Allyn H12+ Holter Recorders Recalled for Defibrillation Safety Non-Compliance

    Welch Allyn is recalling H12+ Holter Recorders and patient cables because they may not meet defibrillation withstand requirements.

    Product
    H12+ and patient cable for the H12+ Holter Recorders with the following device name: PAT CBL 10WIRE LEADFORM AHA SNAP, PAT CBL 10WIRE LEADFORM IEC SNAP, PAT CBL 10WIRE LEADFORM XL AHA SNAP, PAT CBL 10WIRE LEADFORM XL IEC SNAP. The 24-hour H12+ recorder uses a single AA alkali
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1809-2020·2020-05-06

    Philips Azurion 7 M20 XperGuide Software Recall for Incorrect Overlay Display

    Philips is recalling Azurion 7 M20 systems with XperGuide software because a software defect may display incorrect needle paths if the L-arm is mispositioned.

    Product
    Philips Azurion 7 M20 -XperGuide Software hosted in Interventional Workspot 1.5 when used with the Azurion R2.0 system Interventional fluoroscopic x-ray system System code: 722079
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-1835-2020·2020-05-06

    ICU Medical Cogent Hemodynamic Monitoring System Recalled for Software Issues

    ICU Medical is recalling 83 Cogent Hemodynamic Monitoring Systems due to software issues that may cause inaccurate data, unit shutdown, or loss of display.

    Product
    ICU Medical Cogent Hemodynamic Monitoring System, Cogent Item Number 58400-000, UDI: (01)00840619079499
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1801-2020·2020-05-06

    Philips Azurion 7 M20 X-Ray System Recalled for Loose Screw Risk

    Philips is recalling 162 Azurion 7 M20 angiographic X-ray systems because unspecified torque on C-arm roll motor screws could cause them to become loose.

    Product
    Phillips Azurion 7 M20, Angiographic X-Ray System Code 722079 Image guidance in diagnostic, interventional and minimally invasive surgery procedures for the following clinical application areas: vascular, non-vascular, cardiovascular and neuro procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0929-2020·2020-05-06

    Frozen Flounder Stuffed with Seafood Recalled for Undeclared Milk

    Freedman Food Service is recalling frozen flounder stuffed with seafood because the product may contain undeclared milk.

    Product
    7075931 Flounder Stuffed W/ Seafood FRZN, Net Wt LBS 15.00 (6.80 KG), 20 packages per case
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1747-2020·2020-05-06

    Vascular Solutions Recalls Langston Dual Lumen Catheters Due to Separation Risk

    Vascular Solutions is recalling Langston Dual Lumen Catheters because the inner lumen may separate from the hub during pressure injection.

    Product
    Langston Dual Lumen Catheter 6F Model 5540. For delivery of contrast medium in angiographic studies
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1824-2020·2020-05-06

    Kerr Nexus Universal Trial Kits Recalled for Incorrect Bonding Agent

    Kerr/Pentron is recalling 111 trial kits of Nexus Universal with OptiBond Universal due to a packaging error that included the incorrect bonding agent, potentially increasing the risk of bond failures.

    Product
    Nexus Universal with OptiBond Universal, Universal Adhesive Resin Cement, Trial Kit, Ref # 36990 - Product Usage: The intended use of this device is to be used for the cementation of indirect restorations including veneers, inlays, onlays, bridges, posts, and the cementation of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1711-2020·2020-05-06

    GE Healthcare Recalls Lunar iDXA Bone Densitometers Due to Radiation Risk

    GE Healthcare is recalling 123 Lunar iDXA bone densitometers because a control panel issue may cause the start button to stick, potentially leading to accidental radiation exposure.

    Product
    Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1808-2020·2020-05-06

    Uromedica Recalls ProACT Implantation Instrument Sets Due to Sheath Defects

    Uromedica Inc. is recalling 11 ProACT Implantation Instrument Sets because defective U-channel sheaths may damage ProACT implant devices during use.

    Product
    ProACT Implantation Instrument Set, is a reusable, steam sterilizable surgical instrument set consisting of a U-Channel Sheath through which the Pro ACT balloon implant is introduced.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1821-2020·2020-05-06

    Alcon Air Optix Night & Day Aqua Contact Lenses Recalled for Counterfeit Concerns

    Allied Vision Group is recalling specific lots of Alcon Air Optix Night & Day Aqua contact lenses because potentially counterfeit products and packaging were imported to the U.S.

    Product
    Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1827-2020·2020-05-06

    Capso Vision Recalls CapsoCAM Plus Capsule Endoscopy Systems

    Capso Vision is recalling 1,882 CapsoCAM Plus capsule endoscopy systems because a defect in the capsule window may cause the housing to crack and leak during use.

    Product
    CapsoCAM Plus, UDI: 00867770000209
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-1799-2020·2020-05-06

    Beckman Coulter Recalls Barbiturates Reagent Due to Potential Test Inaccuracy

    Beckman Coulter is recalling SYNCHRON Systems Barbiturates Reagent because cross-reactivity testing may not meet claims, potentially causing false positive or negative results.

    Product
    SYNCHRON Systems Barbiturates Reagent (BARB 1 X 250); Catalog No. 475012 - Product Usage: BARB reagent, in conjunction with UniCel DxC 600/800 System(s) and SYNCHRON Systems Drugs of Abuse Testing (DAT) Urine Calibrators, is intended for the qualitative determination of barbitura
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1819-2020·2020-05-06

    Welch Allyn ECG Lead Sets Recalled for Defibrillation Safety Non-Compliance

    Welch Allyn is recalling 78,521 ECG lead sets because they may not meet defibrillation withstand safety requirements.

    Product
    Replaceable lead set for the Wireless Acquisition Module (WAM), which is the ECG front-end for various Electrocardiographs. Sold under the following device names: LEAD SET WAM 10 WIRE BANANA AHA GRAY, LEAD SET WAM 10 WIRE BANANA IEC GRAY, RPLCE LD SET WAM/AM12 LIMBS BANA AHA G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1823-2020·2020-05-06

    U&I Corp. Recalls Velofix SA Cervical Cages Due to Dimensional Defects

    U&I Corp. is recalling 42 Velofix SA cervical cages because screw-hole dimensions may be out of range, posing a risk of screw pullout or instability.

    Product
    Velofix SA cervical cage, REF: TSA161207, TSA161208, TSA161209, TSA161210, TSA161407, TSA161408, TSA161409, TSA161410 - Product Usage:The device is indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disk disease at one level fr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0922-2020·2020-05-06

    Tops Mint Dark Chocolate Bars Recalled for Undeclared Milk

    Tops Markets is recalling Mint Flavor Pure Dark Chocolate bars because they contain undeclared milk, a major allergen.

    Product
    Tops Mint Flavor Pure Dark Chocolate 45% Cocoa NET WT 3.5 oz.(100g)
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1814-2020·2020-05-06

    Welch Allyn X12+ Telemeter and Patient Cable Recall for Defibrillation Safety

    Welch Allyn is recalling X12+ Telemeters and patient cables because they may not meet defibrillation withstand requirements.

    Product
    X12+ and patient cable for the X12+ Telemeter with the following device name: PAT CBL 10WIRE LEADFORM AHA SNAP, PAT CBL 10WIRE LEADFORM IEC SNAP, PAT CBL 10WIRE LEADFORM XL AHA SNAP, PAT CBL 10WIRE LEADFORM XL IEC SNAP, PAT CBL 4WIRE AHA SNAP HC.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1709-2020·2020-05-06

    GE Healthcare Recalls Lunar iDXA Bone Densitometers Due to Radiation Risk

    GE Healthcare is recalling 123 Lunar iDXA bone densitometers because a control panel defect may cause the start button to stick, potentially leading to accidental radiation exposure.

    Product
    Lunar iDXA bone densitometer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1712-2020·2020-05-06

    GE Healthcare Recalls Lunar iDXA Bone Densitometers Due to Radiation Risk

    GE Healthcare is recalling 123 Lunar iDXA bone densitometers because a control panel defect may cause the start button to stick, potentially leading to accidental radiation exposure.

    Product
    Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v18) bone densitometer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1829-2020·2020-05-06

    Baxter Prismaflex System Recall for Connector Safety Information

    Baxter is recalling 1,225 Prismaflex Systems to communicate safety information regarding the proper use of connectors.

    Product
    Prismaflex System, Prismaflex Control Unit
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1830-2020·2020-05-06

    Baxter Prismaflex System Safety Communication on Connector Use

    Baxter issued a safety communication regarding the proper use of connectors with the Prismaflex System and Control Unit.

    Product
    Prismaflex System, Prismaflex Control Unit
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1807-2020·2020-05-06

    Stryker Neptune E-SEP Blade Electrode Recalled for Expired Product

    Stryker is recalling 40 units of Neptune E-SEP 165mm Blade Electrodes shipped to Canada because they were expired due to a distribution error.

    Product
    Neptune E-SEP 165mm Blade Electrode, Catalog Number 0703-165-001 - Product Usage: The Neptune E-SEP is an Integrated Smoke Evacuation Pencil (pencil) designed for general electrosurgical applications including cutting and coagulation, and for removing smoke generated by electrosu
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1820-2020·2020-05-06

    Smiths Medical Recalls Mislabeled Portex Lumbar Puncture Trays

    Smiths Medical ASD Inc. is recalling 100 units of Portex Lumbar Puncture Trays because the inner trays were mislabeled with an incorrect model number.

    Product
    Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product Usage: Portex lumbar puncture trays provide all the materials necessary to measure cerebrospinal fluid pressure and/or collect cerebrospinal fluid specimens. Key components include skin prep materials, la
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1798-2020·2020-05-06

    Boston Scientific Recalls MoXy Laser Fiber for Breakage Risk

    Boston Scientific is recalling MoXy Laser Fibers to update instructions and reduce the likelihood of metal cap and fiber tip breakage.

    Product
    MoXy Laser Fiber, Material Number 0010-2400 - Product Usage: The fiber can be used for the surgical incision/excision, vaporization, ablation, hemostasis and coagulation of soft tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1804-2020·2020-05-06

    Boston Scientific Recalls iLab Polaris Systems Due to Data Archiving Bug

    Boston Scientific is recalling 150 iLab Polaris and Ultrasound systems in Europe because a software bug prevents specific data from being archived without notifying the user.

    Product
    iLab Polaris Multi-Modality Guidance System; iLab Ultrasound Imaging System
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1800-2020·2020-05-06

    Bio-Rad Autoimmune EIA Anti-Tissue Transglutaminase IgA Test Recalled for Lot Bias

    Bio-Rad Labs is recalling 376 units of the Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test, Lot 18200A, due to elevated lot-to-lot bias affecting antibody measurements.

    Product
    Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test; Material Number 425-2260; Lot number 18200A - Product Usage: The assay is an aid in the diagnosis of celiac disease (gluten-sensitive enteropathy) and should be used in conjunction with other serological tests and clinic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1805-2020·2020-05-06

    Obalon Balloon System Recalled Due to Touchscreen Calibration Issues

    Obalon Therapeutics is recalling 45 Obalon Balloon Systems because the touchscreen may lose calibration, preventing balloon inflation.

    Product
    Obalon Balloon System with Model 4300 Touch Dispenser Touchscreen; Software version 02.00.00.0076 - Product Usage: The System is intended to be used as an adjunct to a moderate intensity diet and behavior modification program. All balloons must be removed 6 months after the first
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0921-2020·2020-05-06

    XinXing Dried Plum Recalled for Mislabeling Dried Peaches

    Rong Shing Trading NY Inc is recalling XinXing Dried Plum because the product contains dried peaches, which are not listed on the front label.

    Product
    XinXing Dried Plum, Net Wt. 5.3 oz.(150g)
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1795-2020·2020-05-06

    Becton Dickinson Recalls CareFusion Safe-T-Centesis Catheter Drainage Trays

    Becton Dickinson is recalling 900 units of CareFusion Safe-T-Centesis Catheter Drainage Trays because the 8 Fr catheter was manufactured with a 6.9 Fr needle instead of the correct 8 Fr needle.

    Product
    CareFusion Safe-T-Centesis Catheter Drainage Tray, Sterile, For Single Use Only, Rx only, Catalog Number PIG1280T, UDI Number 01)10885403108402(17) 210930(10)0001304986
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-1797-2020·2020-05-06

    Siemens Atellica CH 930 Analyzer Recall for Software Defect

    Siemens is recalling Atellica CH 930 Analyzers with specific software versions due to a defect that may cause incorrect test results.

    Product
    Atellica CH 930 Analyzer, Siemens Material Number 11067000 with software version v1.21.0 SP1 or lower
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1833-2020·2020-05-06

    Baxter Prismaflex System Recall for Connector Usage Safety Information

    Baxter Healthcare is issuing a Class II recall for 133 Prismaflex Systems to communicate safety information regarding the proper use of connectors.

    Product
    Prismaflex System, Prismaflex Control Unit
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Drugs)·D-1256-2020·2020-05-06

    Dr. Reddy's Recalls Esomeprazole Magnesium Capsules Due to Discoloration

    Dr. Reddy's Laboratories is recalling 1,752 bottles of Esomeprazole Magnesium 40 mg capsules because the product contains brown pellets.

    Product
    ESOMEPRAZOLE MAGNESIUM — ESOMEPRAZOLE MAGNESIUM (ESOMEPRAZOLE MAGNESIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0926-2020·2020-05-06

    Calci-Max Dietary Supplement Recalled for Zinc Content Deficiency

    Alfa Vitamins Laboratories is recalling Calci-Max dietary supplements because FDA testing found the product contained 0.0% of the labeled zinc content.

    Product
    CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL
    Category
    Food
    Distribution
    0 states
  • LowFDA (Food)·F-0930-2020·2020-05-06

    Golden Nutrition Recalls Biotin Supplement Due to Low Content

    Golden Nutrition is recalling Biotin 1000mcg tablets because FDA testing found the biotin content was only 0.8% of the label claim.

    Product
    Biotin 1000mcg, Dietary Supplement, 30 Tablets, Manufactured by: Golden Nutrition
    Category
    Food
    Distribution
    0 states
  • LowFDA (Devices)·Z-1834-2020·2020-05-06

    Ortho VITROS TT4 Reagent Pack Recalled for Calibration Failures

    Ortho Clinical Diagnostics is recalling VITROS TT4 Reagent Packs due to increased unsuccessful calibrations. The recall affects 3,181 units distributed in the US and 23 other countries.

    Product
    VITROS Immunodiagnostic Products TT4 Reagent Pack, Product Code 8744468
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V249000·2020-05-05

    Blue Bird Recalls Vision Buses Due to Fuel Line Chafing Risk

    Blue Bird is recalling 2018-2021 Vision buses with Ford 6.8L engines because parking brake cables may chafe fuel lines, creating a fire risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, VISION TRANSIT BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V251000·2020-05-05

    Freightliner M2 Trucks Recalled for Potential Loss of Drive Power

    Daimler Trucks is recalling 2019 Freightliner Business Class M2 trucks because a wire harness connector may unplug, causing sudden loss of drive power and power steering.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V252000·2020-05-05

    Thomas Built Buses Recalls Saf-T-Liner HDX for Small Emergency Exit Labels

    Daimler Trucks North America is recalling 2010-2020 Thomas Built Buses Saf-T-Liner HDX school buses because the rear emergency exit window labels may have lettering that is too small to read easily.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V248000·2020-05-04

    Hyundai Recalls 2016 Genesis Coupe Due to Air Bag Mounting Bolt Issue

    Hyundai is recalling 2016 Genesis Coupe vehicles because driver-side air bag mounting bolts may be insufficiently tightened, posing an injury risk in a crash.

    Product
    HYUNDAI — HYUNDAI GENESIS COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E027000·2020-05-03

    Harbor Freight Recalls Pittsburgh Automotive 3 Ton Heavy Duty Steel Jack Stands

    Harbor Freight is recalling Pittsburgh Automotive 3 Ton Heavy Duty Steel Jack Stands because the ratchet teeth may not engage properly, causing the stand to fail under load.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-05022020·2020-05-02

    Chicken Noodle Soup Recalled for Undeclared Egg Allergen

    USDA issued a public health alert for Roundy's chicken noodle soup containing undeclared egg. No illnesses have been reported.

    Product
    Roundy's Supermarkets, Inc. — FSIS Issues Public Health Alert for Chicken Noodle Soup Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·20116·2020-05-01

    Epson Recalls Scanner Power Adapters Due to Fire and Burn Hazards

    Epson is recalling power adapters sold with V-series scanners because they can overheat, melt, and catch fire. Consumers should stop using them and contact Epson for a free replacement.

    Product
    Power adapters sold with Epson scanners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V245000·2020-05-01

    Aprilia Motorcycles Recalled for Front Brake Pad Corrosion Risk

    Piaggio is recalling 3,287 Aprilia motorcycles because front brake pads may corrode and detach, increasing stopping distance and crash risk.

    Product
    APRILIA — APRILIA TUONO RF, RSV4 RR, RSV4 RF, TUONO RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V246000·2020-05-01

    Mercedes-Benz Recalls 2020 GLB 250 for Water Intrusion Electrical Risk

    Mercedes-Benz is recalling 2020 GLB 250 vehicles because water entering the foot wells may damage electrical components, causing the instrument cluster to go blank or the engine to stall.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V247000·2020-05-01

    Mercedes-Benz Recalls G-Class Vehicles Due to Child Safety Lock Label Error

    Mercedes-Benz is recalling 2019-2020 G550 and G63 vehicles because the child safety lock symbol may indicate the incorrect status, posing a risk to unrestrained children.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G 550, G63
    Category
    Vehicle
    Distribution
    Distributed nationwide

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