The Recall Desk

Archive

February 2015 recalls

651 recalls were announced in February 2015.

What the numbers show

Critical
223
Severe
185
High
173
Moderate
60
Low
10

Of the 651 recalls this month scored against our rubric, 34% are Critical, 28% are Severe.

1–100 of 651

  • SevereNHTSA·15V114000·2015-02-27

    Dodge Charger and Challenger Recall for Fuel Leak Fire Risk

    Chrysler is recalling 2015 Dodge Charger and Challenger SRT vehicles because a fuel rail hose may leak, increasing the risk of a vehicle fire.

    Product
    DODGE — DODGE CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V113000·2015-02-27

    GM Recalls 2015 Chevrolet Cruze for Parking Brake Cable Bracket Defect

    General Motors is recalling 2015 Chevrolet Cruze vehicles because parking brake cable brackets may not be properly fastened, increasing the risk of the vehicle rolling away.

    Product
    CHEVROLET — CHEVROLET CRUZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V116000·2015-02-27

    Nissan Recalls 2013-2015 Altima Vehicles for Hood Latch Defect

    Nissan is recalling 2013-2015 Altima vehicles because the secondary hood latch may fail to engage, allowing the hood to open while driving.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·036-2015·2015-02-26

    Sunset Farm Foods Recalls Sausage for Undeclared Soy Allergen

    Sunset Farm Foods is recalling approximately 42,669 pounds of link sausage products due to misbranding and an undeclared soy allergen.

    Product
    Sunset Farm Foods, Inc. — Sunset Farm Foods, Inc Recalls Sausage Products Due To Misbranding And Undeclared Allergen
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-1209-2015·2015-02-25

    Del Monte Apple Slices Recalled for Listeria Contamination Risk

    Del Monte is recalling Snack Pack Apple Slices with Caramel Dip due to potential Listeria monocytogenes contamination. The product was distributed in California.

    Product
    Del Monte Snack Pack Apple Slices w. Litehouse Caramel Dip 5 ounces UPC: 7-17524-71943-0
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1221-2015·2015-02-25

    Happy Apples Cinnamon Crunch Caramel Apple Recalled Due to Listeria Outbreak

    Lochirco Fruit & Produce Inc. is recalling Happy Apples Cinnamon Crunch Caramel Apple products linked to a Listeria monocytogenes outbreak.

    Product
    Happy Apples Cinnamon Crunch Caramel Apple, Net Wt. 3.5 oz., with Best By Date range - 8/25-11/23/2014, Responsible firm name on label is Happy Apple Inc., Washington, MO., and Orosi, CA.
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1210-2015·2015-02-25

    Del Monte Snack Pack Apple Slices Recalled for Listeria Risk

    Del Monte is recalling specific lots of Snack Pack Apple Slices with Grapes and Cheese Litehouse Caramel Dip due to potential Listeria monocytogenes contamination.

    Product
    Del Monte Snack Pack Apple Slices w. Grapes & Cheese Litehouse Caramel Dip 7 ounces UPC: 7-17524-77394-4
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1214-2015·2015-02-25

    Lochirco Recalls Caramel Apples Linked to Listeria Outbreak

    Lochirco Fruit & Produce Inc. is recalling specific Happy Apples and Kroger caramel apple products linked to a Listeria monocytogenes outbreak.

    Product
    Caramel Apples packaged in the following configurations with Best By date range - 8/25-11/23/2014, Responsible firm name on label is Happy Apple Inc., Washington, MO., and Orosi, CA.,: Happy Apples Simply Caramel Value 3 Pack, Net Wt. 9 oz., Happy Apples Simply Caramel 4 Pac
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1217-2015·2015-02-25

    FDA Recalls Caramel Apples Linked to Listeria Outbreak

    Lochirco Fruit & Produce Inc. is recalling specific Happy Apple and Kroger branded caramel apples with peanuts due to a Listeria monocytogenes outbreak.

    Product
    Caramel Apples with Peanuts, with Best By date range - 8/25-11/23/2014, Responsible firm name on label is Happy Apple Inc., Washington, MO., and Orosi, CA., packaged in the following configurations: Happy Apples, Net Wt. 3.75 oz., Happy Apples 3 Pack, Net Wt. 9 oz., Happy
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1215-2015·2015-02-25

    Caramel Apples Recalled Due to Listeria Outbreak Link

    Lochirco Fruit & Produce Inc. is recalling specific caramel apples because CDC epidemiologists linked a Listeria monocytogenes outbreak to the product.

    Product
    Caramel Apple Topped with Chocolate & Peanuts with Best By Date range - 8/25-11/23/2014, Responsible firm name on label is Happy Apple Inc., Washington, MO., and Orosi, CA., packaged in the following configurations: Happy Apples Select 3 Pack, Net Wt. 12 oz., Happy Apples Se
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Drugs)·D-0392-2015·2015-02-25

    Hospira Recalls Lactated Ringer's Injection Due to Confirmed Mold Particulates

    Hospira Inc. is recalling 142,644 bags of Lactated Ringer's and 5% Dextrose Injection USP due to confirmed mold particulates in the solution.

    Product
    LACTATED RINGER'S and 5% DEXTROSE Injection USP, 1000 mL, flexible containers, Rx Only, Hospira, Inc., Lake Forest, IL 600045, NDC 0409-7929-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1216-2015·2015-02-25

    FDA Recalls Caramel Apples Linked to Listeria Outbreak

    Lochirco Fruit & Produce Inc. is recalling Happy Apples Crunch Topping Caramel Apples because CDC epidemiologists linked a Listeria monocytogenes illness outbreak to the product.

    Product
    Happy Apples Crunch Topping Caramel Apples, Net Wt. 3.5 oz., with Best By date range - 8/25-11/23/2014, Responsible firm name on label is Happy Apple Inc., Washington, MO., and Orosi, CA.
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1207-2015·2015-02-25

    Del Monte Harvest Blend Salad Recalled for Listeria Contamination

    Del Monte Fresh Produce is recalling 7-Eleven FRESH TO GO Harvest Blend salads due to potential Listeria monocytogenes contamination.

    Product
    7-Eleven FRESH TO GO Harvest Blend 4 ounces UPC: 0-52548-55825-3
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1218-2015·2015-02-25

    Caramel Apples Recalled Due to Listeria Outbreak Link

    Lochirco Fruit & Produce Inc. is recalling specific caramel apple products because CDC epidemiologists linked a Listeria monocytogenes outbreak to them.

    Product
    Caramel Apple packaged topped with colored sprinkles packaged in the following configurations with Best By Date range - 8/25-11/23/2014, Responsible firm name on label is Happy Apple Inc., Washington, MO., and Oro si, CA.,: Happy Apples Wacky, Net Wt. 3.75 oz., Happy Apples Spoo
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1219-2015·2015-02-25

    Caramel Apples Recalled Due to Listeria Outbreak Link

    Lochirco Fruit & Produce Inc. is recalling specific Happy Apples and Kroger Candy Apples because CDC epidemiologists linked a Listeria monocytogenes outbreak to caramel apples.

    Product
    Caramel Apples with red cinnamon, topped with peanuts packaged in the following configurations with Best By Date range - 8/25-11/23/2014, Responsible firm name on label is appy Apple Inc., Washington, MO, and Orosi, CA, : Happy Apples, 1 Apple, Net Wt. 3.75 oz., Happy Apples, V
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1211-2015·2015-02-25

    Del Monte Apple Slices Recalled Due to Listeria Contamination Risk

    Del Monte Fresh Produce is recalling 10-ounce cans of Apple Slices in California due to potential Listeria monocytogenes contamination.

    Product
    Del Monte Apple Slices 10 ounces UPC: 7-17524-72093-1
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-1035-2015·2015-02-25

    GE Healthcare MRI Systems Recalled for Potential Ferrous Object Removal Delay

    GE Healthcare is recalling MRI systems because a disconnected MRU could delay the removal of ferrous objects, posing a life-threatening injury risk.

    Product
    This correction applies to all GE Healthcare MRI systems with superconducting magnets: Discovery MR450, Discovery MR750, Signa HDx, Signa HDxt, Signa HDi, GE 1.5T Signa HDe, Optima MR360, Brivo MR355, Signa Excite-HD 1.5T & 3T, Signa Excite 1.5T HD Twinspeed, Signa Excite 1.5T HD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1220-2015·2015-02-25

    FDA Recalls Happy Apples Grand Gourmet Pecan Caramel Apples Due to Listeria

    Lochirco Fruit & Produce Inc. is recalling Happy Apples Grand Gourmet Pecan Caramel Apples because CDC epidemiologists linked a Listeria monocytogenes outbreak to caramel apples.

    Product
    Happy Apples Grand Gourmet Pecan Caramel Apple packaged in the following configurations with Best By Date range - 8/25-11/23/2014, Responsible firm name on label is Happy Apple Inc., Washington, MO., and Oro si, CA.,: Grand Gourmet, Net WT. 11 oz. and
    Category
    Food
    Distribution
    9 states
  • SevereNHTSA·15V111000·2015-02-25

    McNeilus Recalls Bridgemaster V Mixers Due to Parking Brake Defect

    McNeilus is recalling 2005-2014 Bridgemaster V Mixers because the optional parking brake system may fail to maintain required pressure, increasing crash risk.

    Product
    MCNEILUS — MCNEILUS BRIDGEMASTER V MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0391-2015·2015-02-25

    Hospira Recalls Lidocaine Hydrochloride Injection Due to Particulate Matter

    Hospira is recalling specific vials of 1% Lidocaine Hydrochloride Injection because a returned sample contained human hair attached to the stopper.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1208-2015·2015-02-25

    Del Monte and 7-Eleven Green Apple Slices Recalled for Listeria Risk

    Del Monte Fresh Produce North America, Inc. is recalling specific lots of 7-Eleven and Del Monte Green Apple Slices due to potential Listeria monocytogenes contamination.

    Product
    7-Eleven Green Apple Slices 8 ounces UPC: 0-52548-52481-4; Del Monte Green Apple Slices 12 ounces UPC: 7-17524-71909-6
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1206-2015·2015-02-25

    Del Monte Fruit Mania Recalled for Listeria Contamination Risk

    Del Monte Fresh Produce is recalling 7-Eleven and Circle K Fruit Mania products due to potential Listeria monocytogenes contamination.

    Product
    7-Eleven FRESH TO GO Fruit Mania 6 ounce UPC 0-52548-51982-7; No brand name sold at Circle K stores Fruit Mania 6 ounce UPC 7-17524-77638-9
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1126-2015·2015-02-25

    CME America Recalls BodyGuard 323 Infusion Pumps for Over-Delivery Risk

    CME America is recalling BodyGuard and BodyGuard 323 infusion pumps due to a potential for over-delivery of medication.

    Product
    BodyGuard 323 pump, models 100-510PXSI, 100-516PXS, 100-517PXS, 100-518PXS, 100-603XSA and 100-603XSAP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1128-2015·2015-02-25

    Mako Surgical Recalls Restoris Partial Knee Application RIO Due to Burr Malfunction

    Mako Surgical Corporation is recalling 228 units of the Restoris Partial Knee Application RIO because the surgical burr may continue spinning outside the intended boundary after controls are released.

    Product
    Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use with the Robotic Arm Interactive Orthopedic System (RIO), is indicated for use in surgical knee procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V112000·2015-02-25

    Farber Specialty Vehicles Recalls Wheelchair Lifts Due to Cracking Risk

    Farber Specialty Vehicles is recalling specialty vehicles equipped with Ricon wheelchair lifts because the platform side plates may crack, posing a risk of injury.

    Product
    WINNEBAGO — WINNEBAGO, FREIGHTLINER, FORD WFJ33S, MBC, XCS, F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1205-2015·2015-02-25

    Condies Foods Recalls Salsas Due to Undeclared Peanut Allergen

    Condies Foods is recalling specific salsa products because they contain cumin that may have undeclared peanut protein.

    Product
    Dr. J's Smart Gourmet SalsaMedium, 15 oz., UPC: 793573939166 (Medium).
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1224-2015·2015-02-25

    Probar Recalls Frosted Peanut Butter Bars for Undeclared Milk Allergen

    Probar LLC is voluntarily recalling specific lots of Frosted Peanut Butter BASE Protein Bars due to the possible presence of an undeclared milk allergen.

    Product
    PROBAR Frosted Peanut Butter BASE Protein Bar, 2.46 oz film wrapped bar packaged in 12 wrapped units per sleeve/carton. Unit UPC:8-53152-10060-5. 12 count box UPC: 8-53152-10061-2.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1061-2015·2015-02-25

    Alltech Medical Systems Recalls Two MRI Systems Due to Safety Feature Failure

    Alltech Medical Systems America Inc is recalling two Echostar Spica 1.5T MRI systems because the emergency magnetic field lowering feature may not work correctly.

    Product
    Echostar Spica 1.5T MRI system, for magnetic resonance imaging of the body.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1127-2015·2015-02-25

    Nidek MC-500 Laser Photocoagulator Recalled for Spot Size Control Defect

    Nidek Inc is recalling 16 MC-500 Multicolor Laser Photocoagulators because the spot size control may turn by itself, posing a risk of unintended laser delivery.

    Product
    MC-500 Multicolor Laser Photocoagulator; Indicated for use in retinal photocoagulation for treatment of ocular fundus diseases like diabetic retinopathy, age-related macular degeneration, retinopathy of prematurity and retinal detachment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1203-2015·2015-02-25

    Condies Foods Recalls Salsa Due to Undeclared Peanut Protein

    Condies Foods is recalling Bold & Zesty Salsa because it contains cumin that may have undeclared peanut protein. The product was distributed in Utah and Idaho.

    Product
    Condies Foods, Bold & Zesty Salsa, 14 oz, UPC: 05077744220
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1204-2015·2015-02-25

    Condies and Dr. J's Salsas Recalled for Undeclared Peanut

    Condies Foods is recalling specific salsas because they contain cumin that may have undeclared peanut protein.

    Product
    Dr. J's Smart Gourmet Salsa Mild , 15 oz., UPC: 793573078148
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1222-2015·2015-02-25

    Haitai Tayo Crackers Recalled for Undeclared Milk and Eggs

    Hamchorom is recalling Haitai Tayo Crackers because they contain undeclared milk and eggs, posing a risk to individuals with allergies.

    Product
    Haitai Tayo Crackers, 140 g, 24 boxes/carton, in box colors: blue, yellow, and red.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1212-2015·2015-02-25

    My Sweet Ol' Etcetera Recalls Mint Bars for Undeclared Wheat and Soy

    My Sweet Ol' Etcetera is recalling 36 units of Mint Bars due to undeclared wheat and soy lecithin. The product was distributed in Oregon.

    Product
    Mint Bar, refrigerated, single slice wrapped in cellophane, net wt. 8 oz. The product's label read in parts: "***my sweet ol' etcetera bakery***Mint Bar***Ingredients org flour, org. egg, butter (milk), chocolate, sugar, vanilla, peppermint oil, powdered sugar, butter (milk),
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1116-2015·2015-02-25

    Terumo HX2 Temperature Management System Recalled for Valve Malfunction

    Terumo is recalling 103 HX2 Temperature Management Systems because a malfunctioning mixing valve can cause loss of cooling or heating capability during surgery.

    Product
    Terumo HX2 Temperature Management System provides temperature control of two independent water circuits that directly controls the temperature of patient blood and cardioplegia solution during cardiovascular surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1213-2015·2015-02-25

    My Sweet Ol' Etcetera Recalls Peanut Butter Brownies for Undeclared Soy

    My Sweet Ol' Etcetera is recalling 36 units of Peanut Butter Brownies distributed in Oregon due to undeclared soy lecithin.

    Product
    Peanut Butter Brownie, refrigerated, single slice wrapped in cellophane, net wt. 8 oz. The product's label read in parts: "***New item My sweet ol' etcetera bakery***Peanut Butter brownie, org wheat flour, org. egg, butter, vanilla, sugar, unsw chocolate, Buttercream natural p
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1129-2015·2015-02-25

    Cincinnati Sub-Zero CT-99 Cold Therapy Pad Recall for Seal Separation

    Cincinnati Sub-Zero is recalling CT-99 cold therapy pads because seals may separate during use, causing water leaks.

    Product
    Cold Therapy Pad - cold water circulating pad, one unit per package. The pads are used to provide a patient with local cold therapy by circulating chilled water through the pad that has been positioned on the patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1117-2015·2015-02-25

    Intuitive Surgical Recalls Harmonic Ace Curved Shears Instructions for Use

    Intuitive Surgical is recalling Harmonic Ace Curved Shears Instructions for Use because they incorrectly instruct users on how to manually open the grips.

    Product
    HARMONIC ACE Curved Shears Instructions for Use, 5MM, IS1200; for use with the da Vinci Standard Surgical System. Intended for soft tissue incisions when bleeding control and minimal thermal injury are desired. It is used in conjunction with the da Vinci Surgical System
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1124-2015·2015-02-25

    Teleflex Recalls RUSCH Endotracheal Tubes for Cuff Diameter Labeling Error

    Teleflex is recalling RUSCH Curved Reinforced Endotracheal Tubes because the labeled cuff diameter does not match the actual cuff diameter, though the actual product meets specifications.

    Product
    R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated for airway management. The product may be used to reduce the potential for kinking whenever an unusual positioning of the head or neck is req
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0387-2015·2015-02-25

    Hospira Recalls Vancomycin Hydrochloride Injection Due to Temperature Abuse

    Hospira Inc. is recalling specific lots of Vancomycin Hydrochloride for Injection because they experienced uncontrolled temperature excursions during transit.

    Product
    VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1122-2015·2015-02-25

    Biomet Recalls Specific Lot of Mallory Head Acetabular Shell Components

    Biomet is recalling 17 units of the Mallory Head 4 Finned Acetabular Shell 50 mm (Lot 364600) due to a packaging mix-up with a different shell size.

    Product
    Mallory Head 4 Finned Acetabular Shell 50 mm, PN 13-104150, hip prosthesis component (Ringloc)
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1119-2015·2015-02-25

    Siemens Artis One Angiography System Recalled for Monitor Failure

    Siemens Medical Solutions is recalling one Artis One angiography system because the monitor may fail and require a power cycle to resume operation.

    Product
    Artis One; The Artis One is an angiography system developed for diagnostic interventional procedures including, but not limited to pediatric and obese patients. Procedures that can be performed with the Artis One include cardiac angiography, neuro-angiography, general angiography
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1123-2015·2015-02-25

    Biomet Recalls Acetabular Shell Components Due to Packaging Mix-Up

    Biomet is recalling specific acetabular shell components for hip prostheses due to a packaging mix-up between two different product lots.

    Product
    Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0390-2015·2015-02-25

    Hospira Recalls Vancomycin Hydrochloride Injection Due to Temperature Excursions

    Hospira Inc. is recalling 90,600 vials of Vancomycin Hydrochloride for Injection because the products experienced uncontrolled temperature excursions during transit.

    Product
    VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0388-2015·2015-02-25

    Hospira Recalls Ketorolac Tromethamine Injections Due to Temperature Abuse

    Hospira Inc. is recalling 100 vials of Ketorolac Tromethamine Injection due to uncontrolled temperature excursions during transit. The product was limited to one shipment to a distributor.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1121-2015·2015-02-25

    Pulsiocath PiCCO ProAQT Monitoring Kit Recalled for Packaging Defects

    Pulsion Medical Inc is recalling 90 units of the Pulsiocath PiCCO ProAQT Monitoring Kit due to cracks and holes found in the primary packaging.

    Product
    Pulsiocath PiCCO ProAQT Monitoring Kit, single-use cardiac output (CO) sensor, one unit per plastic sterilizable package. Product Usage: Measures cardiac output by the thermodilution method, measurement of arterial blood pressure, and for cardiac output determination by arte
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1130-2015·2015-02-25

    Haemonetics TEG Hemostasis System Level II Control Recall

    Haemonetics is recalling specific lots of TEG Hemostasis System Level II Control kits because they produce high Maximum Amplitude results outside the expected quality control range.

    Product
    Haemonetics TEG Hemostasis System Level II Control, Catalog number: 8002. Level II Control is a biological control for use with the Thrombelastograph (TEG) Hemostasis System.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1118-2015·2015-02-25

    Intuitive Surgical Recalls Harmonic Ace Curved Shears Instructions for Use

    Intuitive Surgical is recalling 12,467 Harmonic Ace Curved Shears Instructions for Use because they incorrectly instruct users on how to manually open the grips.

    Product
    HARMONIC ACE Curved Shears Instructions for Use, 8MM, IS2000/IS3000; for use with the da Vinci Surgical System - IS2000 and IS3000. Intended for soft tissue incisions when bleeding control and minimal thermal injury are desired. It is used in conjunction with the da Vinci Surg
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-1125-2015·2015-02-25

    Alive ECG App 2.1.2 Recalled for Application Crashes

    Alivecor is recalling Alive ECG App version 2.1.2 for iOS because the application crashes upon use.

    Product
    Alive ECG App 2.1.2 ( a medical device application for the Apple iOS operating system, intended to be used with the AliveCor Heart Monitor. The AliveCor Heart Monitor is intended to record, store and transfer single-channel electrocardiogram (ECG) rhythms. The AliveCor Heart Moni
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·15T007000·2015-02-24

    Alliance Tires Recalled for Tread Separation Risk

    Alliance Tire Americas is recalling specific model 396 tires because the tread may separate, potentially causing a rapid loss of air and increasing the risk of a crash.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15083·2015-02-24

    Fanimation Recalls Brewmaster Ceiling Fans Due to Falling Hub Risk

    Fanimation is recalling Brewmaster ceiling fans because the hub holding the blades can separate from the shaft, posing a risk of injury to bystanders.

    Product
    Brewmaster Ceiling Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V107000·2015-02-24

    Prevost Recalls 2014 X3-45 Coaches Due to Seat Belt Defect

    Prevost is recalling 38 model year 2014 X3-45 commuter coaches because the driver's seat belt retractor may not lock properly, increasing injury risk in a crash.

    Product
    PREVOST — PREVOST X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15721·2015-02-24

    Safe Step Walk-In Tubs Recalled Due to Heated Seat Burn Hazard

    Oliver Fiberglass and NuWhirl Systems are recalling about 6,400 Safe Step walk-in tubs because the heated seat can get stuck on and overheat, posing a burn risk.

    Product
    Safe Step Walk-In Tubs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V105000·2015-02-23

    Freightliner Recalls Cascadia Trucks Due to CNG Fuel Hose Corrosion Risk

    Daimler Trucks is recalling 2014-2015 Freightliner Cascadia trucks with specific CNG fuel systems because a hose may corrode and leak gas, increasing fire risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V101000·2015-02-23

    Altec Recalls 2012-2014 Digger Derrick and Aerial Devices for Fire Risk

    Altec is recalling 2012-2014 Digger Derrick and Aerial Device vehicles mounted on Freightliner chassis because a slow-reacting circuit breaker may cause overheating and fire.

    Product
    ALTEC — ALTEC DIGGER DERRICK, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V104000·2015-02-23

    Gulf Stream Recalls 2010-2014 Trailers Due to Incorrect Tire Labels

    Gulf Stream is recalling 2010-2014 Conquest SE, Kingsport, and Trail Master trailers because incorrect tire labels may lead to over-inflation and tire blowouts.

    Product
    GULF STREAM — GULF STREAM CONQUEST SE, KINGSPORT, TRAIL MASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V103000·2015-02-23

    Cruiser RV Recalls 2016 Stryker Toy Trailers Due to Exhaust Fume Risk

    Cruiser RV is recalling 2016 Stryker Toy and Stryker Toy Hauler trailers with optional slide floors because occupants may be exposed to exhaust fumes.

    Product
    CRUISER RV — CRUISER RV STRYKER TOY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V100000·2015-02-23

    Hyundai Recalls Elantra Vehicles Due to Power Steering Loss Risk

    Hyundai is recalling 2008-2010 Elantra and 2009-2010 Elantra Touring vehicles because the electronic power steering system may disable, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI ELANTRA TOURING, ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V102000·2015-02-23

    Keystone Recalls 2013-2015 RVs Due to Failing Entry Step Rivets

    Keystone RV Company is recalling 5,390 Montana, Raptor, and Dutchmen Voltage vehicles because entry step rivets may shear, causing the steps to fail and increasing the risk of falls.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN RAPTOR, MONTANA, VOLTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·035-2015·2015-02-20

    ESS Food Recalls Pork Belly Produced Without Import Inspection

    ESS Food is recalling pork belly produced in Poland that was not inspected at the U.S. point of entry. No adverse reactions have been reported.

    Product
    ESS Food Recalls Pork Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    2 states
  • CriticalUSDA FSIS·034-2015·2015-02-19

    Kenosha Beef International Recalls Ready-to-Eat Beef Patties for Listeria Risk

    Kenosha Beef International is recalling approximately 21,427 pounds of ready-to-eat beefsteak patties due to possible Listeria monocytogenes contamination.

    Product
    Kenosha Beef International, Ltd. — Kenosha Beef International Recalls Beef Product Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·15V098000·2015-02-19

    Toyota Recalls 2015 Yaris Vehicles for Rear Axle Bearing Bolt Issue

    Toyota is recalling 2015 Yaris vehicles because improperly tightened rear axle bearing bolts may loosen, potentially causing the wheel to lock up or damage brake components.

    Product
    TOYOTA — TOYOTA YARIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V095000·2015-02-19

    Can-Am Recalls 2013 Spyder RT Motorcycles Due to Engine Overheating Risk

    Bombardier Recreational Products is recalling 2013 Can-Am Spyder RT motorcycles because prolonged idling or slow riding in warm weather may cause high engine temperatures, increasing the risk of skin burns or fire.

    Product
    CAN-AM — CAN-AM SPYDER RT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V094000·2015-02-19

    Freightliner M2 Brake Warning Recall Due to Switch Incompatibility

    Daimler Trucks is recalling 2015 Freightliner Business Class M2 vehicles because brake warning lights may not illuminate correctly, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V097000·2015-02-19

    Hyundai Recalls 2015 Genesis Vehicles for Tail Light Water Leak

    Hyundai is recalling 2015 Genesis vehicles because water may leak into tail lights, causing incorrect gear displays or delayed gear engagement, which increases crash risk.

    Product
    HYUNDAI — HYUNDAI GENESIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E012000·2015-02-19

    Meritor Recalls Front Non-Drive Axles Due to Tie Rod Torque Issue

    Meritor is recalling specific front non-drive axles because tie rod nuts may not be properly torqued, which could lead to a loss of vehicle control.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1049-2015·2015-02-18

    Full Tilt Bumberberry Ice Cream Recalled for Listeria Risk

    Full Tilt Ice Cream is recalling Bumberberry ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.

    Product
    Bumberberry ice cream, labeled in part, "***Full Tilt ice cream BUMBERBERRY***Ingredients: Cream, milk, sugar, skim milk, Washington blackberries, Washington blueberries, Washington strawberries, Washington raspberries, guar gum, carob bean gum, soy lecithin, carrageenan***Seattl
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1058-2015·2015-02-18

    Full Tilt Vanilla Bean Ice Cream Recalled for Listeria Risk

    Full Tilt Ice Cream is recalling Vanilla Bean ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.

    Product
    Vanilla Bean ice cream, labeled in part, "***Full Tilt ice cream Vanilla Bean ***Ingredients: Cream, milk, skim milk powder, sugar, vanilla extract, vanilla beans, corn syrup solids, carob bean gum, guar gum, soy lecithin, carrageenan***Seattle WA 98106 www.fulltilticecream.com**
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1103-2015·2015-02-18

    Numbskull LLC Recalls Dirt Ice Cream Due to Listeria Risk

    Numbskull LLC is recalling approximately 650 gallons of Dirt ice cream because raw materials may be contaminated with Listeria monocytogenes.

    Product
    Dirt ice cream; Bulk product is labeled with flavor name and date code, which is affixed to the plastic container (1, 1.5 and 3 gallon).
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1033-2015·2015-02-18

    Whole Foods Recalls Mixtress Bleating Heart Cheese for Listeria Risk

    Whole Foods Market is recalling Mixtress Bleating Heart cheese sold in California, Arizona, and Hawaii due to potential Listeria monocytogenes contamination.

    Product
    Cheese sold unde the brand name, MIXTRESS BLEATING HEART NEW JERSEY COW MILK RAW SHEEPS MILK SALT CULTURES. Sold with a Whole Foods Market scale label in clear plastic wrap. Variable weight item.
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1036-2015·2015-02-18

    Whole Foods Recalls Goldette Tommette Cheese for Listeria Risk

    Whole Foods Market is recalling Goldette Tommette cheese in California, Arizona, and Hawaii due to potential Listeria monocytogenes contamination.

    Product
    Cheese sold under the brand name, Goldette Tommette Bleating Heart, Ingredients: Raw Jersey Cow Milk, Salt, Cultures Contains Milk: 032814. Sold with a Whole Foods Market scale label in clear plastic wrap. Variable weight item.
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1037-2015·2015-02-18

    Whole Foods Recalls Fat Bottom Girl Cheese for Listeria Risk

    Whole Foods Market is recalling Fat Bottom Girl cheese sold in California, Arizona, and Hawaii due to potential Listeria monocytogenes contamination.

    Product
    Cheese sold under the brand name, Fat Bottom Girl, Ingredients: Raw sheeps' milk, salt, cheese cultures Contains Milk: 071612. Sold with a Whole Foods Market scale label in clear plastic wrap. Variable weight item.
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Devices)·Z-1051-2015·2015-02-18

    Teleflex Recalls MAQUET SERVO Humidifiers Due to Cracked Flex Tubes

    Teleflex Medical is recalling MAQUET SERVO Humidifier 163 units because cracks may occur in the corrugated flex tube, posing a risk to patients.

    Product
    MAQUET, SERVO Humidifier 163, Rx Only, Inmed Mfg. Sdn Bhd. Catalog No: XKC01-06-8125-8, Model No. 01-06-8125-8. A heat and moisture condenser (artificial nose) is a device intended to be positioned over a tracheotomy (a surgically created opening in the throat) or tracheal tu
    Category
    Medical Device
    Distribution
    4 states
  • CriticalFDA (Food)·F-1070-2015·2015-02-18

    Rosa Maria Ground Cumin Recalled for Undeclared Peanut Protein

    N.A.C. Foods is recalling Rosa Maria Ground Cumin because it may contain undeclared peanut protein. The product was distributed in New Jersey, New York, and Pennsylvania.

    Product
    Rosa Maria Ground Cumin, (Comino Molido), 6 oz. (173g), UPC 707425-16041-7, Packed by NAC Foods Corp., Palisades Park, NJ.
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1050-2015·2015-02-18

    Full Tilt Dark Chocolate Ice Cream Recalled for Listeria Risk

    Full Tilt Ice Cream is recalling Dark Chocolate ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.

    Product
    Dark Chocolate ice cream, labeled in part, "***Full Tilt ice cream Dark Chocolate***Ingredients: Cream, milk, skim milk powder, sugar, skim milk, bittersweet chocolate, Dutch process cocoa, vanilla, corn syrup solids, chocolate liquor, carob bean gum, guar gum, soy lecithin, carr
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1145-2015·2015-02-18

    Numbskull LLC Recalls Strawberry Ice Cream Due to Listeria Risk

    Numbskull LLC is recalling bulk strawberry ice cream because raw materials may be contaminated with Listeria monocytogenes. The product was distributed to scoop shops and restaurants in Washington and Idaho.

    Product
    Strawberry ice cream; Bulk product is labeled with flavor name and date code, which is affixed to the plastic container (1, 1.5 and 3 gallon).
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1195-2015·2015-02-18

    Freeland Foods Recalls Go Raw Organic Spice Seed Mix Due to Salmonella

    Freeland Foods Inc. is recalling Go Raw Organic Spice Seed Mix because the FDA found Salmonella in the product. Consumers should stop using the recalled items.

    Product
    Go Raw Organic Spice Seed Mix; Net Wt. 1 lb (454 g) USDA Organic UPC 8 59888 00040 Ingredients: Sprouted Organic Pumpkin Seeds, Sprouted Organic Sunflower seeds, Organic Jalapeno, Organic Cilantro, Organic Lime Juice, Organic Spices, Celtic Sea Salt, Organic Garlic Powder
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1163-2015·2015-02-18

    Numbskull LLC Recalls Black Raspberry Gelato Due to Listeria Risk

    Numbskull LLC is recalling Black Raspberry Gelato because raw materials may be contaminated with Listeria monocytogenes. The product was sold in Washington and Idaho.

    Product
    Black Raspberry Gelato; 5 liter plastic trays. Product is labeled with flavor name and production code.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1179-2015·2015-02-18

    Numbskull LLC Recalls Mango Sorbet Due to Listeria Risk

    Numbskull LLC is recalling approximately 27.5 gallons of bulk Mango Sorbet because raw materials may be contaminated with Listeria monocytogenes. The product was distributed to ice cream shops and restaurants in Washington and Idaho.

    Product
    Mango Sorbet; Bulk product is labeled with flavor name and date code, which is affixed to the plastic container (1, 1.5 and 3 gallon).
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1061-2015·2015-02-18

    Full Tilt Ice Cream Recalled for Potential Listeria Contamination

    Full Tilt Ice Cream is recalling Sub Pop Grunge ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.

    Product
    Sub Pop Grunge ice cream, labeled in part, "***Full Tilt ice cream SUB POP***Ingredients: Cream, milk, skim milk, sugar, chocolate covered espresso beans (espresso beans, unsweetened chocolate, sugar, cocoa fat, soy lecithin, vanilla) coffee, carob bean gum, guar gum, soy lecithi
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1140-2015·2015-02-18

    Numbskull LLC Recalls S'Morchata Ice Cream Due to Listeria Risk

    Numbskull LLC is recalling S'Morchata ice cream because raw materials may be contaminated with Listeria monocytogenes. The product was distributed to scoop shops and restaurants in Washington and Idaho.

    Product
    S'Morchata ice cream; Bulk product is labeled with flavor name and date code, which is affixed to the plastic container (1, 1.5 and 3 gallon).
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1051-2015·2015-02-18

    Full Tilt Green Tea Chip Ice Cream Recalled for Listeria Risk

    Full Tilt Ice Cream is recalling Green Tea Chip ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.

    Product
    Green Tea Chip ice cream, labeled in part, "***Full Tilt ice cream Green Tea Chip***Ingredients: Cream, milk, skim milk, sugar, green tea powder, Chocolate Chips (unsweetened chocolate, sugar, cocoa fat, soy lecithin, vanilla), corn syrup solids, carob bean gum, guar gum, soy lec
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1115-2015·2015-02-18

    Numbskull LLC Recalls Mango Ice Cream Due to Listeria Risk

    Numbskull LLC is recalling mango ice cream because raw materials may be contaminated with Listeria monocytogenes. The product was distributed to scoop shops and restaurants in Washington and Idaho.

    Product
    Mango ice cream; Bulk product is labeled with flavor name and date code, which is affixed to the plastic container (1, 1.5 and 3 gallon).
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1098-2015·2015-02-18

    Numbskull LLC Recalls Coconut Brownie Ice Cream Due to Listeria Risk

    Numbskull LLC is recalling Coconut Brownie ice cream because raw materials may be contaminated with Listeria monocytogenes. The product was distributed to Washington and Idaho scoop shops and restaurants.

    Product
    Coconut Brownie ice cream; Bulk product is labeled with flavor name and date code, which is affixed to the plastic container (1, 1.5 and 3 gallon).
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1162-2015·2015-02-18

    Numbskull LLC Recalls Choc Mint Chip Gelato Due to Listeria Risk

    Numbskull LLC is recalling Choc Mint Chip Gelato because raw materials may be contaminated with Listeria monocytogenes. The product was sold in Washington and Idaho.

    Product
    Choc Mint Chip Gelato; 5 liter plastic trays. Product is labeled with flavor name and production code.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1178-2015·2015-02-18

    Numbskull Lemon Sorbet Recalled for Potential Listeria Contamination

    Numbskull LLC is recalling approximately 64 gallons of bulk Lemon Sorbet because raw materials may be contaminated with Listeria monocytogenes.

    Product
    Lemon Sorbet; Bulk product is labeled with flavor name and date code, which is affixed to the plastic container (1, 1.5 and 3 gallon).
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1034-2015·2015-02-18

    Whole Foods Recalls Moolicious Blue Cheese for Listeria Risk

    Whole Foods Market is recalling Moolicious Blue Bleating Heart raw cow milk cheese sold in California, Arizona, and Hawaii due to potential Listeria monocytogenes contamination.

    Product
    Cheese sold under the brand name, MOOLICIOUS BLUE BLEATING HEART RAW COW MILK SALT CULTURES. Sold with a Whole Foods Market scale label in clear plastic wrap. Variable weight item.
    Category
    Food
    Distribution
    3 states

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