The Recall Desk

Archive

March 2021 recalls

387 recalls were announced in March 2021.

What the numbers show

Critical
11
Severe
150
High
165
Moderate
46
Low
15

Of the 387 recalls this month scored against our rubric, 3% are Critical, 39% are Severe.

Which agencies issued them

201–300 of 387

  • SevereFDA (Devices)·Z-1212-2021·2021-03-17

    FDA Recalls CervAlign Anterior Cervical Plate System Due to Locking Mechanism Failure

    RTI Surgical is recalling CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 26mm Material Number: 66-226 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1207-2021·2021-03-17

    RTI Surgical Recalls CervAlign Anterior Cervical Plate System Due to Locking Failure

    RTI Surgical is recalling specific CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 16mm Material Number: 66-116 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0334-2021·2021-03-17

    Westminster Cracker Inc. Recalls Oyster Crackers Due to Plastic Foreign Object

    Westminster Cracker Inc. is recalling specific oyster cracker products because they may contain hard plastic foreign objects. Consumers should check their pantries for the affected items.

    Product
    Old Cape Cod Soup and Chowder Oyster Crackers - 8oz Box, 12 per case - UPC 093215801005; Westminster Bakers Co. Soup & Snack Crackers - 8oz Box, 12 per case - UPC 093215200426; Westminster Bakers Co. Soup & Snack Crackers - 8oz Box, 6 per case - UPC 093215200426
    Category
    Food
    Distribution
    13 states
  • HighFDA (Devices)·Z-1179-2021·2021-03-17

    Draeger VentStar Watertrap Breathing Circuits Recalled for Detachment Risk

    Draeger Medical is recalling 150 units of VentStar Watertrap (N) 180 breathing circuits because the Y-piece may detach, causing a leak that hinders patient ventilation.

    Product
    VentStar Watertrap (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP00363 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1178-2021·2021-03-17

    Dräger VentStar Basic Breathing Circuits Recalled for Detachment Risk

    Draeger Medical is recalling 1,525 VentStar Basic breathing circuits because a Y-piece may detach, causing a leak that hinders patient ventilation.

    Product
    VentStar Basic (N) 180- Drager Breathing Circuits/Anesthesia Sets Order Number: MP00353 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V185000·2021-03-17

    2021 Hyundai Santa Fe Air Bag Child Detection System Defect

    2021 Hyundai Santa Fe vehicles have a defective Occupant Detection System that may fail to prevent air bag deployment when a child restraint is detected in the front passenger seat, increasing crash injury risk.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V186000·2021-03-17

    2021 Nissan Rogue Incorrect Wheel Nuts May Cause Wheel Separation

    Nissan is recalling certain 2021 Rogue vehicles with incorrect wheel nuts that may loosen and cause wheel vibration. This vibration may break wheel studs and cause wheel separation, increasing crash risk.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V184000·2021-03-17

    Jayco Travel Trailers Recalled for Potential Gas Leak Risk

    Jayco is recalling 2019-2020 travel trailers because a stove component may cause a gas leak, increasing fire risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK, JAY FEATHER, JAY FLIGHT SLX, JAY FLIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1181-2021·2021-03-17

    Getinge Flow i Anesthesia Systems Recalled for Absorber Docking Failures

    Getinge Group Logistics America is recalling 144 Flow i Anesthesia Systems due to complaints of incorrect FiCO2 readings and System Check Out failures when docking the absorber.

    Product
    Anesthesia gas-machine - Product Usage: intended for use in administering anesthesia while controlling the entire ventilation of patients with no ability to breathe, as well as in supporting patients with limited ability to breathe.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1180-2021·2021-03-17

    Dräger ID Circuit Basic Breathing Circuits Recalled for Detachment Risk

    Dräger Medical is recalling ID Circuit Basic (N) 180 breathing circuits because the Y-piece may detach, causing a leak that hinders patient ventilation.

    Product
    ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP01327 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1175-2021·2021-03-17

    Canon Medical System INFX-8000C C-Arm Recall for X-Ray Field Shift

    Canon Medical System is recalling 272 INFX-8000C C-arm systems nationwide because the x-ray irradiation field may shift relative to the displayed image at certain angles.

    Product
    System INFX-8000C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1203-2021·2021-03-17

    Insulet Recalls Omnipod DASH User Guides Due to Decimal Error

    Insulet Corporation is recalling 21,723 Omnipod DASH User Guides distributed outside the US due to a misprint regarding decimal separators that could lead to incorrect bolus delivery.

    Product
    Omnipod DASH Insulin Management System User Guide (OUS Only) Product Catalog Number: PT 000002 XXX XXX XX PT 000318 PT 000319 Distributed to: Canada (French only), the Netherlands, France, Austria, Germany, Belgium, Greece, Turkey, Norway, Sweden, Denmark, and Finland
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1202-2021·2021-03-17

    Thermo Fisher Recalls Cascadion Clinical Analyzer Due to Software Defect

    Thermo Fisher Scientific is recalling 19 Cascadion Clinical Analyzers because a software defect may cause false Vitamin D deficiency results.

    Product
    Cascadion SM Clinical Analyzer, REF 99990000 SN Type: 9910
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-0337-2021·2021-03-17

    Hu Chocolate-Covered Hunks Recalled for Undeclared Almonds

    Hu Products LLC is recalling Chocolate-Covered Hunks Sour Goldenberries because the product may contain undeclared almonds.

    Product
    Hu***CHOCOLATE-COVERED HUNKS SOUR GOLDENBERRIES***Net Wt. 4 oz (113g); packaged in a black bag; Distributed by: Hu Products LLC, NY, NY 10011
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1186-2021·2021-03-17

    Stryker Recalls Triathlon Knee Baseplates Due to Manufacturing Defect

    Stryker is recalling 11 Triathlon Tritanium Tibial Baseplates because a manufacturing defect may prevent the knee insert from locking securely.

    Product
    Prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer.
    Category
    Medical Device
    Distribution
    13 states
  • HighFDA (Devices)·Z-1182-2021·2021-03-17

    Sunstar G.U.M. Hydral Dry Mouth Spray Recalled for Bacterial Contamination

    Sunstar Americas is recalling 56,960 bottles of G.U.M. Hydral Dry Mouth Relief Oral Spray due to potential Burkholderia cepacia contamination.

    Product
    SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray, 2 FL.OZ. UPC0 70942 30713 0 - Product Usage: The device is formulated with water, moisturizers /humectants including one plant-based moisture rich humectant, sweeteners and flavors that collectively have lubricating, mo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21097·2021-03-17

    HOFISH Recalls Mattresses for Federal Flammability Standard Violation

    HOFISH is recalling 10-inch hybrid mattresses sold on Amazon.com because they fail to meet the mandatory federal flammability standard, posing a fire hazard.

    Product
    HOFISH 10-Inch Hybrid Certi-PUR Certified Foam and Pocket Spring Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1187-2021·2021-03-17

    Tosoh Thyroglobulin Antibody Calibrator Recalled for Calibration Failures

    Tosoh Bioscience Inc is recalling specific lots of Thyroglobulin Antibody Calibrators because some combinations with AIA PACKS resulted in unacceptable calibration values.

    Product
    Thyroglobulin Antibody (TgAB) Calibrator - Product Usage: intended for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of anti-thyroglobulin antibodies (TgAb) in human serum on specific TOSOH AIA System analyzers. Measurements obtained by this device aid in the dia
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1184-2021·2021-03-17

    MedComp Recalls Power Injectable CT Port Kits with Incorrect Port Size

    Medical Components, Inc. is recalling 96 Power Injectable CT Port kits because they contain 6.6F ports instead of the correct 5F size, which may prolong surgical procedures.

    Product
    Power Injectable CT Port insertion kits - Product Usage: is an implantable access device designed to provide repeated access to the vascular system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1189-2021·2021-03-17

    Physio-Control Recalls LIFEPAK CR2 Defibrillators Due to Missing Lid Magnets

    Physio-Control is recalling 89,763 LIFEPAK CR2 defibrillators because missing lid magnets may cause premature battery depletion.

    Product
    PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator is designed for indoor and outdoor use in a stationary environment. After the electrode pads are applied, the fully automatic model evaluates the heart rhythm and, if a shockable rhythm is det
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1188-2021·2021-03-17

    Siemens Dimension Vista HDLC Reagent Cartridges Recalled for Erroneous Results

    Siemens Healthcare Diagnostics is recalling Dimension Vista HDLC reagent cartridges due to discolored reagents that may cause erroneous test results.

    Product
    Dimension Vista HDLC - colorimetric method, lipoproteins - Product Usage: used as an aid in the diagnosis of lipid disorders (such as diabetes mellitus), various liver and renal diseases, and in the assessment of risk for atherosclerosis and cardiovascular disease.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0333-2021·2021-03-17

    Sapphire Exchange Recalls Yum Crumbs for Undeclared Red #40

    The Sapphire Exchange is recalling Yum Crumbs, Strawberry Shortcake, due to undeclared Red #40. The voluntary recall covers 3,421 bottles distributed domestically.

    Product
    YUM CRUMBS, STRAWBERRY SHORTCAKE, 12 oz and 32 oz
    Category
    Food
    Distribution
    0 states
  • LowFDA (Food)·F-0332-2021·2021-03-17

    One Degree Organic Foods Recalls Gluten Free Sprouted Rolled Oats

    One Degree Organic Foods is recalling 448,720 packages of Gluten Free Sprouted Rolled Oats due to rancidity and packaging integrity defects.

    Product
    One Degree Organic Foods Gluten Free Sprouted Rolled Oats NET WT. 5 lbs (80 oz) 2.27 kg UPC:6 75625 32318 8
    Category
    Food
    Distribution
    11 states
  • LowFDA (Devices)·Z-1183-2021·2021-03-17

    OraSure Methamphetamine Test Kit Recalled for Incorrect Reagent Lot Labeling

    OraSure Technologies is recalling 16 units of Methamphetamine Intercept Microplate kits due to a labeling error where the wrong lot number was printed on the box.

    Product
    Methamphetamine Intercept Microplate kit EIA - IVD qualitative determination of methamphetamine in oral fluid, PN 11041C.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0299-2021·2021-03-17

    Ferring Recalls Menopur Due to Out-of-Specification pH in Diluent

    Ferring Pharmaceuticals is recalling Menopur (menotropins) and its 0.9% Sodium Chloride diluent because the diluent failed pH specifications. The recall covers products distributed nationwide in the USA.

    Product
    MENOPUR — MENOPUR (MENOTROPINS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V181000·2021-03-16

    Peterbilt 536 Recalled for Engine Control Module Software Defect

    PACCAR is recalling one 2021 Peterbilt 536 truck because incorrect engine software may prevent safety features like braking and stability control from functioning properly.

    Product
    PETERBILT — PETERBILT 536
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V180000·2021-03-16

    Jayco Recalls 2021 Embark and Reatta Motorhomes Due to Gas Leak Risk

    Jayco is recalling 2021 Embark and Entegra Reatta motorhomes because an incorrectly routed LP furnace hose may cause a gas leak, increasing the risk of fire or explosion.

    Product
    JAYCO — JAYCO, ENTEGRA EMBARK, REATTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V179000·2021-03-16

    Highland Ridge RV Recalls Fifth Wheels and Travel Trailers Due to Gas Leak Risk

    Highland Ridge RV is recalling 2019-2020 fifth wheels and travel trailers because an overtightened bolt may damage the stove's O-ring seal, causing a gas leak and increasing fire risk.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW MESA RIDGE, OPEN RANGE, SILVERSTAR, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V178000·2021-03-16

    2021 Keystone Cougar Trailers Recalled for Electrical Shock Hazard in Inverter

    Certain 2021 Keystone Cougar trailers equipped with the Off the Grid Solar package may have an incorrectly wired inverter that energizes the shore power connection, posing an electrical shock risk. Keystone will repair the inverter at no charge.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V176000·2021-03-15

    2021 BMW 430i and M440i side-thorax airbags may fail to deploy

    2021 BMW 430i and M440i models have defective side-thorax airbags that may not deploy during side-impact crashes, increasing injury risk. Owners should contact their dealer for a free software update.

    Product
    BMW — BMW 430I, M440I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V177000·2021-03-15

    Ditch Witch Trailers Recalled for Missing Side Reflectors

    Charles Machine Works is recalling specific Ditch Witch trailers because they may be missing side reflex reflectors, which reduces visibility to other drivers.

    Product
    DITCH WITCH — DITCH WITCH ZS6S, S4S, 745-7900, 025-1020
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V174000·2021-03-12

    ARBOC Specialty Vehicles Recalls 2021 Spirit of Freedom Due to Fuel Leak

    ARBOC is recalling 29 units of the 2021 Spirit of Freedom because a fuel hose may not be secured correctly, creating a fire risk.

    Product
    ARBOC SPECIALTY VEHICLES — ARBOC SPECIALTY VEHICLES SPIRIT OF FREEDOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-03122021-01·2021-03-12

    Vons Chicken Noodle Soup Recalled for Incorrect Gluten-Free Labeling

    USDA FSIS issued a public health alert for Vons Signature CAFÉ Chicken Noodle Soup due to misbranding. The product is labeled gluten-free but contains wheat, posing a risk to consumers with gluten allergies.

    Product
    The Vons Companies, Inc. — FSIS Issues Public Health Alert for Chicken Soup Product Due to Misbranding
    Category
    Food
    Distribution
    12 states
  • HighNHTSA·21V172000·2021-03-12

    2021 Coachmen Viking Travel Trailers Cooktop Fire Risk Recall

    Forest River, Inc. is recalling certain 2021 Coachmen Viking and Clipper travel trailers because the cooktop may not be properly isolated from the furnace return air, which can cause the flame to invert and increase fire risk. Dealers will install and seal a panel free of charge.

    Product
    COACHMEN — COACHMEN CLIPPER, VIKING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V171000·2021-03-12

    ATC Recalls 2018-2021 ARV Trailers Due to Insufficient Safety Chains

    ATC is recalling 2018-2021 ARV Gamechanger and Pro Bumper Pull trailers because the installed safety chains are rated lower than the trailer's axle capacity, posing a crash risk.

    Product
    ATC ARV — ATC ARV PRO BUMPER PULL, GAMECHANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V169000·2021-03-11

    Nissan Recalls Altima and Titan Vehicles for Tire Sidewall Defect

    Nissan is recalling 2018-2021 Titan and 2019-2020 Altima vehicles equipped with Continental tires that may have been over-cured, posing a risk of sudden air loss and loss of vehicle control.

    Product
    NISSAN — NISSAN TITAN, ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V170000·2021-03-11

    Nissan Recalls 2020 Murano Vehicles for Steering Link Defect

    Nissan is recalling 2020 Murano vehicles because a steering transverse link may separate, potentially causing loss of vehicle control and increasing crash risk.

    Product
    NISSAN — NISSAN MURANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V165000·2021-03-11

    Honda Recalls 2019-2020 Pilot and Passport Vehicles for Tire Defect

    Honda is recalling 2019-2020 Pilot and Passport vehicles equipped with specific Continental tires that may have been overcured during production, posing a risk of tire failure and loss of vehicle control.

    Product
    HONDA — HONDA PILOT, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V164000·2021-03-11

    2021 Kia K5 Air Bag Detection System Recall for Child Restraint Safety

    Kia is recalling certain 2021 K5 vehicles because the occupant detection system may fail to recognize child restraints, risking air bag deployment during a crash.

    Product
    KIA — KIA K5, FORTE, TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V168000·2021-03-11

    Land Rover Recalls 2020 Range Rover Evoque for Knee Air Bag Defect

    Land Rover is recalling 2020 Range Rover Evoque vehicles because the left-side lower knee air bag cushion cover may come loose, potentially reducing protection in a crash.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V167000·2021-03-11

    Jaguar Recalls 2020 F-Type Vehicles Due to ABS Software Defect

    Jaguar is recalling 2020 F-Type vehicles because a startup diagnostic check may fail, potentially disabling the Anti-Lock Brake System and Dynamic Stability Control.

    Product
    JAGUAR — JAGUAR F-TYPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V163000·2021-03-11

    2021 RAM Cummins Diesel Cab Chassis Trucks Recalled for Electrical Fire Risk

    Chrysler is recalling approximately 19,214 2021 RAM heavy-duty trucks with diesel engines due to a potential electrical short in the intake heater relay that could cause vehicle fires. Owners should not park these vehicles indoors until repaired.

    Product
    RAM — RAM 5500, 2500, 3500, 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0325-2021·2021-03-10

    See's Candies Chocolate Bunnies Recalled for Salmonella Contamination Risk

    Thompson Brands LLC is recalling specific See's Candies chocolate bunny products and Gold Foil Balls due to potential Salmonella contamination. All affected units are on hold and have not been distributed to consumers.

    Product
    1. See's Candies brand chocolate 4.5 oz Sitting Bunny (SKU 600738) 2. See's Candies brand 1 oz Bunny (SKU 600741) 3. Gold Foil Balls (SKU 600144) (note: firm also uses the term 'rabbit' interchangeably with 'bunny' however product labeling states bunny or bunnies)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1159-2021·2021-03-10

    ReNovo Recalls Reprocessed Medical Devices Shipped as Sterile

    ReNovo, Inc. is recalling 81 units of reprocessed medical devices that were shipped to customers labeled as sterile but were non-sterile.

    Product
    Various reprocessed products: PROVISION, Reprocessed Smith and Nephew Arthroscopic Shavers, STERILE EO; PROVISION Reprocessed Depy Mitek Ablation Electrodes, VAPR COOLPULSE 90 deg; PROVISION Reprocessed Smith and Nephew Trocars/ Cannulas (Class I); PROVISION Reprocessed Con
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V158000·2021-03-10

    Ford Recalls Vehicles for Driver-Side Airbag Inflator Explosion Risk

    Ford is recalling specific 2006-2012 vehicles because the driver-side airbag inflator may explode, potentially causing serious injury or death.

    Product
    MERCURY — MERCURY, LINCOLN, FORD MILAN, MKZ, ZEPHYR, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V162000·2021-03-10

    Mazda Recalls 2007-2009 B-Series Trucks for Air Bag Inflator Defect

    Mazda is recalling 2007-2009 B-Series trucks because the driver's side air bag inflator may explode, posing a risk of serious injury or death to occupants.

    Product
    MAZDA — MAZDA B-SERIES TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V160000·2021-03-10

    Hyundai Recalls Genesis Vehicles Due to ABS Module Fire Risk

    Hyundai is recalling 2015-2020 Genesis and G80 vehicles because the ABS module could short circuit and cause a fire. Owners should park outside until the fuse is replaced.

    Product
    GENESIS — GENESIS, HYUNDAI G80, GENESIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V155000·2021-03-10

    Ford Recalls 15,769 Vehicles Due to Tire Curing Defect

    Ford is recalling 15,769 vehicles equipped with Continental tires that may have been over-cured during production. This defect can cause sudden air loss or tread loss, increasing the risk of a crash.

    Product
    FORD — FORD ESCAPE, F-150, F-350 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1156-2021·2021-03-10

    Hamilton Heater Shaker Recalled Due to Fire Risk from Flammable Liquids

    Hamilton Co is recalling 4,729 Heater Shaker units because flammable liquids entering the device can cause a fire.

    Product
    HAMILTON HEATER SHAKER, 115 VAC/ 230 VAC, 750 VA, Power Consumption 41V/ 100W (max.), Relative Humidity 15% - 85% no condensation. REF 19903400
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Devices)·Z-1157-2021·2021-03-10

    BioFire Film Array BCID Panels Recalled for False Positive Risk

    BioFire Diagnostics is recalling Film Array BCID Panels due to an increased risk of false positive Pseudomonas aeruginosa results when used with specific BD BACTEC vials.

    Product
    Gram-Negative Bacteria And Associated Resistance Markers; Film Array Blood Culture Identification (BCID); Film Array BCID Panel - Product Usage: intended for use with FilmArray systems. Part No: RFIT-ASY-0126 / UDI: 00815381020086 Part No: RFIT-ASY-0127 / UDI: 00815381020093
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0326-2021·2021-03-10

    Vallarta Organic Basil Recalled for Cyclospora Contamination

    Vallarta Organic LLC is recalling organic basil contaminated with Cyclospora cayetanensis. The product was distributed in Virginia.

    Product
    ALBAHACA ORGANICA/BASIL, 460 gm x Bag, 15 Bags
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1160-2021·2021-03-10

    United Imaging X-ray System Recalled for Uncommanded Motion Hazard

    Shanghai United Imaging Healthcare is recalling six X-ray systems because the tube head may move unexpectedly, posing a collision risk to patients.

    Product
    Digitial Medica X-ray Imagining System, Model: uDR 596i, RX, CE0123, UDI:(01) 06971576833023 - Product Usage: intended to used by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21093·2021-03-10

    Hillsdale Jennings Counter and Bar Stools Recalled for Fall Hazard

    Hillsdale Furniture is recalling Jennings counter and bar stools because the seat can break off the base, posing a fall hazard.

    Product
    Hillsdale Furniture Jennings Counter and Bar Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V153000·2021-03-10

    Mercedes-Benz Sprinter Recalled for Sliding Door Lock Defect

    Daimler Vans USA is recalling 2019-2020 Mercedes-Benz Sprinter vans with optional electric sliding doors because the auxiliary lock may be the incorrect type, potentially increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 2500, SPRINTER 4500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0327-2021·2021-03-10

    Shenandoah Growers Organic Fresh Cut Basil Recalled for Cyclospora Contamination

    Shenandoah Growers is recalling organic fresh cut basil due to possible contamination with Cyclospora. Consumers should check their pantries for affected products.

    Product
    Organic fresh cut basil packaged in plastic clamshell containers. Shenandoah Growers by Thats Tasty, 0.75 oz UPC: 7-68573-00101-4 Shenandoah Growers by Thats Tasty, 2.0 oz UPC: 7-68573-02143-2 Shenandoah Growers by Thats Tasty 4.0 oz UPC: 7-68573-00141-0 Shenandoah Growers by
    Category
    Food
    Distribution
    10 states
  • HighNHTSA·21V156000·2021-03-10

    2021 BMW XB7, X5, and X7 Head Restraints May Detach in Crash

    BMW is recalling certain 2021 XB7, X5, and X7 vehicles because the head restraints on second-row outer seats may be an incorrect type and could detach during a crash, increasing injury risk.

    Product
    BMW — BMW X7, XB7, X5, X5 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V159000·2021-03-10

    Audi passenger air bag may not deploy correctly in certain model years

    Volkswagen Group (Audi) is recalling certain 2019-2021 Audi models for defective passenger air bags that may not deploy properly during a crash. Owners should contact Audi at 1-800-253-2834 for free inspection and repair.

    Product
    AUDI — AUDI A6, A7, A6 ALLROAD, S6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V157000·2021-03-10

    2021 Porsche vehicles recalled for potentially loose suspension components

    Porsche is recalling certain 2021 Taycan, 911, Cayman, Boxster, and 718 Spyder models because suspension components may not have been properly tightened and could loosen, potentially causing loss of vehicle control.

    Product
    PORSCHE — PORSCHE TAYCAN, redundant CAYMAN, redundant BOXSTER, 911
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V161000·2021-03-10

    2019-2021 Genesis G70 Engine Compartment Fire Risk from ABS Module

    Hyundai is recalling 2019-2021 Genesis G70 vehicles because the Anti-Lock Brake System module could short-circuit and cause an engine compartment fire. Owners should park outside until the ABS module fuse is replaced.

    Product
    GENESIS — GENESIS G70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1173-2021·2021-03-10

    Siemens Sensis Vibe Systems Recalled for Potential System Freezes

    Siemens is recalling 37 Sensis Vibe systems in the US because they may sporadically freeze during operation or idle, preventing user interaction.

    Product
    Sensis / Sensis Vibe systems with software version VD12 and equipped with HP Flex Pro-C PC. Diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies Model Numbers: Sensis Vibe Hemo 11007641 Sensis Vibe Combo 11007642 Sensis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V152000·2021-03-10

    Daimler Recalls 2019-2020 Sprinter Vans for Brake Pedal Bolt Issue

    Daimler Vans USA is recalling 2019-2020 Mercedes-Benz and Freightliner Sprinter vans because a brake pedal bolt may detach, causing brake lights to stay on and increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 1500, SPRINTER 2500, SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1151-2021·2021-03-10

    Baxter Recalls PrisMax Hemodialysis Tubing Due to Performance Variability

    Baxter Healthcare is recalling PrisMax System Version II hemodialysis tubing due to performance variability that may cause alarms and therapy interruptions.

    Product
    The PrisMax System Version II Hemodialysis Delivery System: Automatic Repositioning System Pump Assembly, specifically tubing, Model Numbers: a) 955626 b) 955558 c) 955701 PrisMax V2 Preventive Maintenance Kit, Product Code SC616 ARPS PUMP, Product Code SC6035 ARPS Pump As
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1158-2021·2021-03-10

    BioFire BCID2 Panel Recalled for False Positive Pseudomonas Results

    BioFire Diagnostics is recalling BCID2 Panels due to a risk of false positive Pseudomonas aeruginosa results when used with specific BD BACTEC blood culture vials.

    Product
    BioFire BCID2 Panel; IVD, Rx Only Part No: RFIT-ASY-0147 / UDI: 00815381020338 - Product Usage: intended for use with FilmArray systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21092·2021-03-10

    Lifetime Products Recalls 6-Foot Seminar Tables Due to Injury Risk

    Lifetime Products is recalling 6-foot seminar tables because the brace arms may fail to lock, causing the table to collapse and posing an injury risk.

    Product
    Lifetime Products 6-foot Seminar Tables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1161-2021·2021-03-10

    ACIST Kodama Intravascular Ultrasound Catheter Recalled for Damaged O-Ring

    Acist Medical Systems is recalling Kodama Intravascular Ultrasound Catheters because damaged o-ring fragments could be flushed out of the device.

    Product
    ACIST Kodama Intravascular Ultrasound Catheter The Kodama Intravascular Ultrasound Catheter is a component of the ACIST HDi System. The ACIST HDi System is intended to be used for ultrasound examination of coronary and peripheral intravascular pathology. Intravascular ultraso
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0331-2021·2021-03-10

    Urban Remedy Organic Almond Maca Almond Milk Recalled for Undeclared Allergens

    Urban Remedy is recalling 111 units of Organic Almond Maca Almond Milk due to a labeling error that failed to declare almonds and cashews.

    Product
    Urban Remedy Organic Almond Maca Almond Milk; 16 FL. OZ (473 mL) UPC" 8 13377 02102 4 Ingredients: Almond Milk (filtered Water, Almond) Date Syrup, Vanilla Extract, Maca Root PowerCashew Milk (filtered water, cashew, Date syrup, Maca Root Powder, Himalayan Pink Salt. C Cont
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·21E018000·2021-03-10

    Safety Belt Solutions Recalls Seat Belts Due to Heat-Treatment Defect

    Safety Belt Solutions is recalling specific seat belts because the tongues may not have been heat-treated correctly, potentially failing to restrain occupants in a crash.

    Product
    SEAT BELTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0330-2021·2021-03-10

    Urban Remedy Organic Cacao Mocha Cold Brew Coffee Recalled for Allergen Mislabeling

    Urban Remedy is recalling 208 units of Organic Cacao Mocha Cold Brew Coffee in California due to undeclared almonds and cashews.

    Product
    Urban Remedy Organic Cacao Mocha Cold Brew Coffee; 16 FL. OZ (473 mL) UPC" 8 13377 02222 9 Ingredients: Cashew Milk (filtered water, cashew, Date syrup, Vanilla Extract, Himalayan Pink Salt) Cold Brew Coffee (filtered water, coffee bean), Cacoa Powder Contains: Cashew
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1164-2021·2021-03-10

    G & H Wire Company Recalls Orthodontic Elastic Bands Due to Labeling Error

    G & H Wire Company is recalling orthodontic elastic bands because the patient pack text is incorrect, which could lead to misuse and temporary discomfort.

    Product
    Band, Elastic, Orthodontic - Product Usage: Orthodontic elastics, also referred to as rubber bands, are small stretchy loops of rubber that help move teeth into proper alignment during orthodontic treatment. Their purpose is to create additional force for tooth movement in any of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1163-2021·2021-03-10

    Johnson & Johnson Recalls Nonconforming TECNIS Toric Intraocular Lenses

    Johnson & Johnson Surgical Vision Inc is recalling 27 TECNIS Toric 1-Piece Intraocular Lenses due to the release of nonconforming products.

    Product
    TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in the capsular bag.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1155-2021·2021-03-10

    Bovie Medical Recalls ConMed Disposable Bipolar Ablators Due to Packaging Defect

    Bovie Medical Corporation is recalling 5,270 ConMed Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the sterile barrier.

    Product
    ConMed Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0296-2021·2021-03-10

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system is out of specification for mechanical peel.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1172-2021·2021-03-10

    Barco Diagnostic Radiology Display Recalled for Lack of DICOM Compliance

    Barco N.V. is recalling MDNC-3421 diagnostic radiology displays because they were shipped without being DICOM-compliant. These units will not pass required acceptance tests.

    Product
    Barco MDNC-3421 DISPLAY, DIAGNOSTIC RADIOLOGY
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1154-2021·2021-03-10

    Bovie Medical Recalls HNM Disposable Bipolar Ablators Due to Packaging Defect

    Bovie Medical Corporation is recalling 3,862 HNM Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the barrier.

    Product
    HNM Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1153-2021·2021-03-10

    Bovie Velocity Disposable Bipolar Ablators Recalled for Sterile Packaging Defect

    Bovie Medical Corporation is recalling Velocity Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the sterile barrier.

    Product
    Velocity Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1152-2021·2021-03-10

    CooperSurgical Recalls Milex Gellhorn Flexible Pessaries Due to Manufacturing Error

    CooperSurgical is recalling specific lots of Milex Gellhorn Flexible pessaries because they were manufactured with incorrect stem lengths.

    Product
    Milex Gellhorn Flexible under the following labels: 1) Gellhorn Flexible w/Short Stem Pessary, REF MXKPGSS2-1/4, 2-1/4" (57 mm) with Kit, 2) Gellhorn Flexible w/Short Stem Pessary, REF MXPGSS2-1/4, 2-1/4" (57 mm) without Kit, 3) Gellhorn Flexible w/Short Stem Pessary, REF MXPGSS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1170-2021·2021-03-10

    Boston Scientific Recalls Polypectomy Snares Due to Incomplete Pouch Seals

    Boston Scientific is recalling Captivator, Captiflex, and Sensation polypectomy snares because users reported incomplete pouch seals before use.

    Product
    Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares Outer box UPN, Inner pouch UPN: M00560311 (Box 5), M00560310; M00560321 (Box 5), M00560320; M00562651 (Box 5), M00562650; M00562652 (Box 20), M00562650; M00562671 (Box 5), M00562670; M005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0293-2021·2021-03-10

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 473,280 Daytrana (methylphenidate) patches because the delivery system failed mechanical peel specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0292-2021·2021-03-10

    Dr. Reddy's Recalls Progesterone Capsules Due to Dissolution Failures

    Dr. Reddy's Laboratories is recalling 16,449 bottles of 200 mg Progesterone Capsules because stability testing revealed out-of-specification dissolution results.

    Product
    PROGESTERONE — PROGESTERONE (PROGESTERONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0295-2021·2021-03-10

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 786,900 Daytrana (methylphenidate) patches because the delivery system failed mechanical peel specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1162-2021·2021-03-10

    Nihon Kohden Telemetry Recalled for Incorrect Date Stamp or No Data Transfer

    Nihon Kohden America Inc is recalling WMTS Telemetry Receivers because they may display incorrect date stamps or fail to transfer data.

    Product
    WMTS Telemetry Receiver, Multiple Patient Receiver, Model Number/ UDI: ORG 9100A/ 00841983102554 ORG 9110A/ 00841983102561 ORG 9700A/No UDI
    Category
    Medical Device
    Distribution
    46 states
  • LowFDA (Drugs)·D-0298-2021·2021-03-10

    Jubilant Cadista Recalls Methylprednisolone Tablets Due to Illegible Labeling

    Jubilant Cadista Pharmaceuticals is recalling specific lots of Methylprednisolone Tablets USP, 4 MG, due to misaligned printing on the blister card that makes dosing instructions illegible.

    Product
    Methylprednisolone Tablets USP, 4 MG, packaged in a 21-count blister pack, Rx only, Jubilant Cadista Pharmaceuticals, Inc., Salisbury, MD 21801, NDC 59746-001-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0289-2021·2021-03-10

    Sun Pharma Recalls Subpotent Cequa Cyclosporine Ophthalmic Solution Vials

    Sun Pharmaceutical Industries is recalling Lot 10007 of Cequa (cyclosporine) ophthalmic solution because the product is subpotent. The recall covers 37,400 cartons distributed nationwide and in Australia.

    Product
    CEQUA — CEQUA (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1168-2021·2021-03-10

    Boston Scientific Recalls Polypectomy Snares Due to Incomplete Pouch Seals

    Boston Scientific is recalling Captivator and Captiflex polypectomy snares because users reported incomplete pouch seals before patient use.

    Product
    Captivator Single-Use Polypectomy Snares, Captiflex Single-Use Polypectomy Snares. Outer box UPN, Inner Pouch UPN: M00561311 (Box 10), M00561310 M00562301 (Box 10), M00562300; M00562321 (Box 10), M00562320; M00562341 (Box 10), M00562340; M00562451 (Box 10), M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0291-2021·2021-03-10

    Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurities

    Dr. Reddy's Laboratories is recalling Atorvastatin Calcium tablets because they contain impurities that exceed FDA specifications.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1169-2021·2021-03-10

    Boston Scientific Recalls Captivator II Polypectomy Snares Due to Incomplete Seals

    Boston Scientific is recalling Captivator II Single-Use Polypectomy Snares because users reported incomplete pouch seals before use.

    Product
    Captivator II Single-Use Polypectomy Snares Outer box UPN, Inner Pouch UPN: M00561191 (Box 10), M00561190; M00561221 (Box 10), M00561220; M00561222 (Box 20), M00561220; M00561223 (Box 40), M00561220; M00561233 (Box 40), M00561230.
    Category
    Medical Device
    Distribution
    Distributed nationwide

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