The Recall Desk

Archive

December 2017 recalls

389 recalls were announced in December 2017.

What the numbers show

Critical
38
Severe
74
High
172
Moderate
94
Low
11

Of the 389 recalls this month scored against our rubric, 10% are Critical, 19% are Severe.

201–300 of 389

  • HighNHTSA·17V809000·2017-12-15

    Newmar Recalls Motorhomes Due to Defective Kidde Fire Extinguishers

    Newmar is recalling 1995-2018 motorhomes equipped with Kidde fire extinguishers that may clog or detach, increasing injury risk during a fire.

    Product
    NEWMAR — NEWMAR SCOTTSDALE, VENTANA, VENTANA LE, ALL STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V808000·2017-12-15

    Forest River Recalls 2018 Sierra and Sandpiper Trailers for Tire Placard Error

    Forest River is recalling 2018 Sierra and Sandpiper recreational trailers because the Federal Placard incorrectly lists the recommended tire pressure as 110psi instead of 95psi.

    Product
    FOREST RIVER — FOREST RIVER SIERRA, SANDPIPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V810000·2017-12-15

    Daimler Trucks Recalls 2002-2017 Models for Defective Fire Extinguishers

    Daimler Trucks North America is recalling 2002-2017 Freightliner and Western Star trucks because the installed fire extinguishers may clog, require excessive force to activate, or detach nozzles, posing injury risks.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 5700, 4700, 4900, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V802000·2017-12-14

    REV Recalls 2018 Fleetwood and Holiday Rambler Motorhomes for Satellite Dish Defect

    REV Recreation Group is recalling 87 specific 2018 Fleetwood and Holiday Rambler motorhomes because the satellite dish may detach from the roof while driving, creating a road hazard.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER PACE ARROW, NAVIGATOR, BOUNDER, FLAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17T019000·2017-12-14

    Cooper Tires Recalled for Belt Separation Risk

    Cooper Tire & Rubber Co. is recalling specific tire models due to an incorrect belt rubber compound that may cause belt separation and loss of vehicle control.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V806000·2017-12-14

    Mazda Recalls 2004-2006 B-Series Trucks for Air Bag Inflator Defect

    Mazda is recalling 2004-2006 B-Series trucks because the passenger air bag inflator may rupture during deployment, sending metal fragments into the vehicle.

    Product
    MAZDA — MAZDA B-SERIES TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18706·2017-12-14

    Crate and Barrel Recalls Dakota Benches Due to Fall Hazard

    Crate and Barrel is recalling Dakota wooden benches because they can tip over, posing a fall hazard. The company has received reports of injuries including broken bones and an amputation.

    Product
    Crate and Barrel Dakota benches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18059·2017-12-14

    Pier 1 Imports Recalls Glass Pumpkins Due to Laceration Hazard

    Pier 1 Imports is recalling decorative glass pumpkins because the wooden stems can detach, causing the glass to break and cut consumers.

    Product
    Glass pumpkins with wooden stems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V804000·2017-12-14

    2017 Mercedes-Benz and Freightliner Sprinter 3500 Recall for Crosswind Assist Defect

    Daimler Vans USA is recalling 2017 Mercedes-Benz and Freightliner Sprinter 3500 vehicles because the Crosswind Assist system may fail to activate automatic braking in strong crosswinds, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18062·2017-12-14

    Hunter Contempo Ceiling Fans Recalled for Impact Injury Hazard

    Hunter Fan Company is recalling Contempo ceiling fans because incorrect installation instructions may cause the light globe to fall, posing an impact injury hazard.

    Product
    Hunter Contempo ceiling fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0102-2018·2017-12-13

    Pravastatin Tablets Recalled Due to Incorrect Bupropion Filling

    International Laboratories is recalling Pravastatin Sodium Tablets 40 mg because they were filled with Bupropion hydrochloride XL Tablets 300 mg.

    Product
    Pravastatin Sodium Tablets, USP, 40 mg, 30-count bottle, Rx only, Packaged for: International Laboratories, LLC. St. Petersburg, FL 33710, NDC 54458-925-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0437-2018·2017-12-13

    Organic Traditions Dark Chocolate Hazelnuts Recalled for Undeclared Milk

    Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Hazelnuts with Chili due to undeclared milk (casein). The product was distributed in 22 states and D.C.

    Product
    Organic traditions brand DARK CHOCOLATE HAZELNUTS WITH CHILI, NET WT. 3.5 oz. (100 g) - UPC 8 54260 01450 1, and NET WT. 8 oz. (227 g) - UPC 8 54260 00703 9; the product was also distributed in cartons containing 2 x 12 lbs. bulk bags (totaling 24 lbs.). -- Product of Italy --- D
    Category
    Food
    Distribution
    22 states
  • CriticalFDA (Food)·F-0423-2018·2017-12-13

    Working Cow Homemade Inc. Recalls Cookies N Cream Ice Cream

    Working Cow Homemade Inc. is recalling 193 tubs of Cookies N Cream Ice Cream after FDA environmental samples tested positive for Listeria monocytogenes.

    Product
    Cookies N Cream Ice Cream 3 gallons
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0507-2018·2017-12-13

    Goya Adobo Seasoning Recalled for Salmonella Contamination

    Tradewind Foods de Puerto Rico Inc. is recalling Goya Adobo seasoning due to positive Salmonella test results.

    Product
    GOYA Adobo, All Purpose Seasoning with Cumin, Goya Foods, Inc. 28 OZ
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-0106-2018·2017-12-13

    Grande X 5800 Capsules Recalled for Undeclared Prescription Ingredients

    Gadget Island, Inc. is recalling Grande X 5800 capsules because they contain undeclared prescription drugs sildenafil, desmethyl carbodenafil, and tadalafil.

    Product
    grande X 5800 capsule, (Maca Root 120 mg, Horny Goat Weed 120 mg, Guarana Seed 80 mg, Ginko Leaf 60 mg, Saw Palmetto 100 mg, Damiana Leaf 100 mg, Ginseng Root 80 mg, Tribulus Terrestris 90 mg, Tongkat Alo 100 mg, Rhodiola Rosea 60 mg, L-Arginine 90 mg), 1-capsule packets, distri
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0103-2018·2017-12-13

    Gadget Island Recalls Unapproved Rhino 7 Platinum 5000 Capsules

    Gadget Island, Inc. is recalling Rhino 7 Platinum 5000 capsules because they contain undeclared active pharmaceutical ingredients and were marketed without FDA approval.

    Product
    RHINO 7 Platinum 5000, capsule, Proprietary Material: 750mg, 1-capsule packets, distributed by Fifty Shades Bayside, NY 11361, UPC 617135861224
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0506-2018·2017-12-13

    Goya Adobo Seasoning Recalled for Salmonella Contamination

    Tradewind Foods is recalling Goya Adobo seasoning due to positive Salmonella test results found in the plant and finished product.

    Product
    GOYA Adobo, All Purpose Seasoning with Pepper, Goya Foods, Inc. 28 OZ
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0439-2018·2017-12-13

    Organic Traditions Dark Chocolate Almonds Recalled for Undeclared Milk

    Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Almonds with Chili due to undeclared milk (casein). The product was distributed in 22 states and D.C.

    Product
    Organic traditions brand DARK CHOCOLATE ALMONDS WITH CHILI, NET WT. 3.5 oz. UPC 8 54260 01550 8, and NET WT. 8 oz. UPC 8 54260 00707 7; the product was also distributed in cartons containing 2 x 12 lbs. bulk bags (totaling 24 lbs.). -- Product of Italy --- Distributed by Organic
    Category
    Food
    Distribution
    22 states
  • CriticalFDA (Drugs)·D-0104-2018·2017-12-13

    PapaZen 3300 capsules recalled for undeclared prescription ingredients

    Gadget Island, Inc. is recalling PapaZen 3300 capsules because they contain undeclared prescription drugs sildenafil, desmethyl carbodenafil, and tadalafil.

    Product
    PapaZen 3300 capsule, Proprietary Blend 1800mg, 1-capsule packets, distributed by FX Power San Diego, CA 92108, UPC 718122032587
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0105-2018·2017-12-13

    Gadget Island Recalls FIFTY SHADES 6000 Capsules for Undeclared Ingredients

    Gadget Island, Inc. is recalling FIFTY SHADES 6000 capsules because they contain undeclared active pharmaceutical ingredients sildenafil, desmethyl carbodenafil, and tadalafil.

    Product
    FIFTY SHADES 6000 capsule, Proprietary Raw Material 4550, 1-capsule packets, distributed by Express Pac Trading, UPC 4026666146056
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0514-2018·2017-12-13

    Saranac Pasta and Seafood Salad Recalled for Undeclared Crab

    Saranac Brand Foods is recalling specific lots of Pasta and Seafood Salad due to undeclared shellfish (crab). Consumers in Michigan and Wisconsin should check their products.

    Product
    Saranac Pasta and Seafood Salad 2x10lbs or 2x5lbs plastic tubs.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0425-2018·2017-12-13

    Working Cow Homemade Ice Cream Recalled for Listeria Contamination

    Working Cow Homemade Inc. is recalling No Sugar Added Butter Pecan Ice Cream after FDA environmental samples tested positive for Listeria monocytogenes.

    Product
    No Sugar Added Butter Pecan Ice Cream 3 gallons
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·17V805000·2017-12-13

    Honda Recalls VT1300CX Fury Motorcycles for Fuel Tank Weld Defect

    Honda is recalling specific 2010, 2016, and 2017 VT1300CX Fury motorcycles because missing welds on the fuel tank mounting bracket could cause fuel leaks and fire.

    Product
    HONDA — HONDA VT1300CX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0436-2018·2017-12-13

    Organic Traditions Dark Chocolate Hazelnuts Recalled for Undeclared Milk

    Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Hazelnuts because they contain undeclared milk (casein). The products were distributed in 22 states and the District of Columbia.

    Product
    Organic traditions brand DARK CHOCOLATE HAZELNUTS, NET WT. 3.5 oz (100 g) - UPC 8 54260 01400 6, and NET WT. 8 oz (227 g) - UPC 8 54260 00701 5 -- Product of Italy --- Distributed by Organic Traditions - Cheektowaga, NY 14227
    Category
    Food
    Distribution
    22 states
  • SevereNHTSA·17V801000·2017-12-13

    Hyundai Recalls 2018 Santa Fe Sport Vehicles Due to Air Bag Defect

    Hyundai is recalling 2018 Santa Fe Sport vehicles because a side curtain air bag component may detach during deployment, increasing injury risk.

    Product
    HYUNDAI — HYUNDAI SANTA FE SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V799000·2017-12-13

    Forest River Recalls 2016-2018 Berkshire XLT Motorhomes for Fire Risk

    Forest River is recalling 2016-2018 Berkshire XLT motorhomes because incorrect circuit breakers may cause excessive heat and increase the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0193-2018·2017-12-13

    Pro-Med Instruments Recalls DORO Sterile Disposable Skull Pins Due to Breakage

    Pro-Med Instruments is recalling DORO Sterile Disposable Skull Pins because two instances of pin tip breakage were reported during surgery.

    Product
    pmi, pro med instruments, DORO(R) Sterile Disposable Skull Pins, 3 pieces (3 pieces per blister, 12 blisters per box), STERILE R, Rx ONLY The DORO(R) Skull Pins are inserted into the receptacles of the skull clamp and fixate the head during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0438-2018·2017-12-13

    Organic Traditions Dark Chocolate Almonds Recalled for Undeclared Milk

    Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Almonds because the product contains undeclared milk (casein).

    Product
    Organic traditions brand DARK CHOCOLATE ALMONDS, NET WT. 3.5 oz. (100 g) - UPC 8 54260 01500 3, and NET WT. 8 oz. (227 g) - UPC 8 54260 00705 3; the product was also distributed in cartons containing 2 x 12 lbs. bulk bags (totaling 24 lbs.). -- Product of Italy --- Distributed b
    Category
    Food
    Distribution
    22 states
  • HighFDA (Devices)·Z-0196-2018·2017-12-13

    Becton Dickinson Recalls Trypticase Soy Agar Plates Due to Listeria Contamination

    Becton Dickinson is recalling Trypticase Soy Agar with 5% Sheep Blood plates because they are contaminated with Listeria monocytogenes. The affected lots are distributed worldwide.

    Product
    TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM), Catalog Number 221261 Trypticase Soy Agar with 5% or 10% Sheep Blood is used for cultivating fastidious microorganisms and for the visualization of hemolytic reactions produced by many bacterial species.
    Category
    Medical Device
    Distribution
    47 states
  • HighFDA (Devices)·Z-0202-2018·2017-12-13

    GE CARESCAPE Patient Data Module Recalled for Missing Apnea Alarms

    GE Medical Systems is recalling CARESCAPE Patient Data Module software because it fails to generate visual or audible alarms for impedance respiration apnea events.

    Product
    CARESCAPE Patient Data Module (PDM) v2.6 software used with CARESCAPE Monitors B850, B650, and B450 v2.0.7 or earlier software The PDM is intended to provide uninterrupted acquisition of physiologic parameter data on adult, pediatric and neonatal patients during non-transport/be
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0427-2018·2017-12-13

    FLAVORx Sweetening Enhancer Recalled for Microbial Growth

    FLAVORx Inc. is recalling Sweetening Enhancer AQ bottles due to microbial growth detected during stability testing. The product is used as a pharmacy compounding material.

    Product
    FLAVORx Sweetening Enhancer , the product is packaged as follows: "Sweetening Enhancer AQ, 4oz & 1oz Bottles, Lot #161269 / Exp. Date 12/2018 "Sweetening Enhancer AQ, 4oz & 1oz Bottles, Lot #170361 / Exp. Date 03/2019 #100 per box 1oz bottles, #50 per box 4oz bottles
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0426-2018·2017-12-13

    Raley's Purely Made Peanuts Recalled for Potential Macadamia Nut Mislabeling

    New Century Snacks LLC is recalling Raley's Purely Made Dry Roasted Unsalted Peanuts because some packages may be mislabeled as macadamia nuts.

    Product
    Raley's Purely Made Dry Roasted Unsalted Peanuts; 12 oz. (340 g) clear plastic bag. No artificial ingredients. Some packages may be labeled as Raley's Purely Made Macadamia Nuts, 6.5 oz. (184 g) clear bag
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0195-2018·2017-12-13

    ICU Medical Recalls MedNet Medication Management Suite Software

    ICU Medical Inc is recalling MedNet 6.1 and 6.21 software because it may alter piggyback medication settings without user notice.

    Product
    ICU Mednet(TM) Medication Management Suite 6.1 and 6.21, Product Code/List Numbers: (a) 16037-64-01; MedNet 6.1 b) 16037-64-02; MedNet 6.1 c) 16037-64-03; MedNet 6.1 d) 16037-64-04; MedNet 6.21 The ICU Medical MedNet Medication Management Suite (MMS) is intended to faci
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0205-2018·2017-12-13

    FDA Recalls Unapproved Compressible Limb Therapy Systems Due to Incorrect Air Compression

    Won Industry Co. is recalling three unapproved Compressible Limb Therapy Systems because they have incorrect air compression level setups. The devices were distributed in Maryland, Texas, and Mexico.

    Product
    Compressible Limb Therapy System (Leg Cuffs, Arm Sleeves, Waist pads and air injection hoses) Product Usage: Intended for limb massage utilizing air compression. It is specially designed to improve venous and lymphatic circulation by compressing and releasing air pressure pro
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0208-2018·2017-12-13

    Intersurgical Solus Flexible Laryngeal Mask Airways Recalled for Occlusion Risk

    Intersurgical Inc is recalling Solus Flexible wire-reinforced laryngeal mask airways because a defect in the tubing may cause partial or total occlusion when the cuff is over-inflated.

    Product
    Solus Flexible wire-reinforced laryngeal mask airways under the following sizes: 1) small pediatric size 2 catalog #8002001, 2) large pediatric size 2.5 catalog #8025001, 3) small adult size 3 catalog #8003001, 4) medium adult size 4 catalog #8004001 and 5) large adult size 5 ca
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-0197-2018·2017-12-13

    Roche Recalls Accu-Chek Connect App Due to Bolus Advisor Bug

    Roche Diabetes Care is recalling the Accu-Chek Connect app because a bug in the Bolus Advisor feature may prevent correction bolus advice from being available for recent glucose readings.

    Product
    Accu-Chek Connect diabetes management software app, Catalog number 07562462001 / GTIN number 00365702700000, Catalog number 07250452001 / GTIN number 00365702700017 The Accu-Chek Connect Diabetes Management App is indicated as an aid in the treatment of diabetes. The software pr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0415-2018·2017-12-13

    Juanita's OJOS Mexican Pastry Recalled for Undeclared Coconut

    Dominguez Family Enterprises is recalling Juanita's Brand OJOS Mexican Pastry due to undeclared coconut. The product was distributed in Oregon and Washington.

    Product
    Juanita's Brand OJOS Mexican Pastry. Product are pink balls of cake rolled in coconut packed in a flex plastic bag of varying weight. 6 units per bag. UPC 48867 00216.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0210-2018·2017-12-13

    Biosense Webster Recalls SMARTABLATE RF System Generator Units

    Biosense Webster is recalling 185 SMARTABLATE RF System Generators because they may inadvertently deliver RF energy if the foot pedal is placed near Stereotaxis magnets.

    Product
    SMARTABLATE RF System Generator
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Food)·F-0428-2018·2017-12-13

    FLAVORx Sweetening Enhancer Recalled for Microbial Growth

    FLAVORx Inc. is recalling specific lots of Sweetening Enhancer used in pharmacy compounding due to microbial growth detected in stability testing.

    Product
    FLAVORx Sweetening Enhancer , the product is packaged as follows: Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #3281712 / Exp. Date 12/2018 Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle, Lot #4281712 / Exp. Date 03/2019 Fillmaster Auto Sweetening Enhancer
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0433-2018·2017-12-13

    Meijer Cashews Recalled for Undeclared Mixed Nuts

    Meijer Distribution is recalling specific lots of cashews that contain undeclared mixed nuts instead of chocolate covered cashews.

    Product
    Roasted & Salted Cashews and Chocolate Covered Cashews; packaged in clear plastic containers; NET WT 18 oz. (1 LB 2 oz.), 510 g; UPC 8-86926-46877-9
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0430-2018·2017-12-13

    Woldong Kimchi Recalled for Undeclared Sesame Seeds

    H. A. R. Maspeth Corp. is recalling Woldong World's Best Kimchi due to undeclared sesame seeds. The product was distributed in nine states.

    Product
    WOLDONG WORLD'S BEST KIMCHI WHOLE CABBAGE KIMCHI PREMIUM 3LBS (1.36kg), UPC: 8 46034 04853 9 and 7LBS (3.17kg), UPC: 846034048546.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-0446-2018·2017-12-13

    Plow and Hearth Recalls Chocolate Covered Cashews Due to Undeclared Peanuts

    Plow and Hearth is recalling 1,332 units of 10-ounce Cashew Towers because the product contains salted peanuts instead of cashews, posing an undeclared allergen risk.

    Product
    89291 Cashew Tower (Plow and Hearth Chocolate Covered Cashews). Net weight: 10 ounces . The product is package as a Individual can is sealed tin with a plastic lid / Tower is packaged in a clear acetate (plastic) sleeve.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0207-2018·2017-12-13

    BD Precision Glide Needles Recalled for Hub Damage and Leakage

    Becton Dickinson is recalling 2,598,000 BD Precision Glide Needles due to hub damage that can cause breakage or leakage during use.

    Product
    BD Precision Glide Needle 18G x 1 RB, Catalog 305195 Product Usage: These needles are intended for general purpose fluid injection/aspiration, infusion, venipuncture to obtain blood collection and insulin injection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0429-2018·2017-12-13

    FLAVORx Recalls Sweetening Enhancer Due to Microbial Growth

    FLAVORx Inc. is recalling specific bottles of Sweetening Enhancer because testing revealed microbial growth. The product is a pharmacy compounding material.

    Product
    FLAVORx Sweetening Enhancer , the product is packaged as follows: Vet Sweetening Enhancer AQ, 2oz Bottle, Lot #161269 / Exp. Date 12/2018 Package type: Amber Glass Boston Round Bottles
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0420-2018·2017-12-13

    Plow & Hearth Chocolate Covered Cashews Recalled for Undeclared Peanuts

    Virginia Diner Inc. is recalling 60 cans of Plow & Hearth Chocolate Covered Cashews because peanuts were found in the product, posing a risk to individuals with peanut allergies.

    Product
    Plow & Hearth Chocolate Covered Cashews
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0422-2018·2017-12-13

    Leclerc Foods Recalls Fit & Active Protein Bars Due to Plastic Contamination

    Leclerc Foods USA is recalling Fit & Active Chocolatey Chip Protein Meal Bars because flexible pieces of yellow plastic were found in the product.

    Product
    Fit & Active Chocolatey Chip Protein Meal Bars; UPC: 41498 18695; Lot Code: Q209MY; Expiration date: May 24, 2018
    Category
    Food
    Distribution
    21 states
  • ModerateFDA (Food)·F-0447-2018·2017-12-13

    Krispy Kreme Recalls Glazed Blueberry Cake Doughnuts Due to Foreign Matter

    Krispy Kreme is recalling Glazed Blueberry Cake Doughnuts because a foreign matter strand was found in the product. The recall affects 4,041 boxes distributed in Georgia and South Carolina.

    Product
    Krispy Kreme Doughnuts, Glazed Blueberry Cake Doughnuts, Net Wt. 13.5oz (half dozen), Manufactured under the authority of Krispy Kreme Doughnut Corporation, Winston-Salem, NC 27102.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0201-2018·2017-12-13

    Exactech Recalls Vantage Total Ankle Tibial Inserts Due to Labeling Mismatch

    Exactech, Inc. is recalling nine Vantage Total Ankle Tibial Inserts because the inner labeling and packaged device may not match the outer box label.

    Product
    Vantage Total Ankle Tibial Insert, Fixed Bearing, 10 mm, Left, Size 3. Exactech Inc. Intended for patients with ankle joints damage by severe rheumatoid, post-traumatic, or degenerative arthritis. It is also indicated for revision of failed previous reconstructions where suffi
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-0453-2018·2017-12-13

    Krispy Kreme Doughnut Holes Recalled for Foreign Matter Contamination

    Krispy Kreme is recalling Original Glazed Doughnut Holes because a foreign matter strand was found in the product. The recall affects boxes sold in Georgia and South Carolina.

    Product
    Krispy Kreme Doughnuts, Original Glazed Doughnut Holes, Manufactured under the authority of Krispy Kreme Doughnut Corporation, Winston-Salem, NC 27102.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0451-2018·2017-12-13

    Krispy Kreme Recalls Glazed Mini Crullers Due to Foreign Matter

    Krispy Kreme is recalling Glazed Mini Crullers because a foreign matter was found on the product. The recall affects 4,041 boxes and containers distributed in Georgia and South Carolina.

    Product
    Krispy Kreme Doughnuts, Glazed Mini Crullers, Krispy Juniors, Manufactured under the authority of Krispy Kreme Doughnut Corporation, Winston-Salem, NC 27102.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0203-2018·2017-12-13

    Fukuda Denshi Patient Monitor Recall for Damaged Lithium-Ion Capacitor

    Fukuda Denshi is recalling DS-8100M and DS-8100N patient monitors because a damaged lithium-ion capacitor may cause a short-term battery error message.

    Product
    Fukuda Denshi patient monitor model DS-8100M and DS-8100N Product Usage: Use of the Fukuda Denshi DynaScope Model DS-8100N/8100M Patient Monitor is indicated in those situations where observation of one or more of the following parameters on an individual patient may be requi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0204-2018·2017-12-13

    FDA Recalls Two Unapproved Morning Life Air Compression Devices

    Won Industry Co. is recalling two Morning Life air compression devices because they were distributed without FDA approval and have incorrect air compression settings.

    Product
    Morning Life, Model WIC2008S & WIC2008, UDI 8809293 870336 Product Usage: Intended for limb massage utilizing air compression. It is specially designed to improve venous and lymphatic circulation by compressing and releasing air pressure programmed on the device. It helps to
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0209-2018·2017-12-13

    Remel Mueller-Hinton Broth Recalled for Incorrect Cation Labeling

    Remel Inc is recalling 7 units of Mueller-Hinton Broth IVD because the product label may contain incorrect cation information.

    Product
    CM0405 Mueller-Hinton Broth IVD, 500g makes 23.8 litres.
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Food)·F-0449-2018·2017-12-13

    Krispy Kreme Pumpkin Spice Doughnuts Recalled for Foreign Matter

    Krispy Kreme is recalling Glazed Pumpkin Spice Cake Doughnuts because a foreign matter strand was found in the product. The recall affects 4,041 boxes sold in Georgia and South Carolina.

    Product
    Krispy Kreme Doughnuts, Glazed Pumpkin Spice Cake Doughnuts, Net Wt. 13.5oz (half dozen), Manufactured under the authority of Krispy Kreme Doughnut Corporation, Winston-Salem, NC 27102.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0452-2018·2017-12-13

    Krispy Kreme Doughnuts Recalled for Foreign Matter Contamination

    Krispy Kreme is recalling specific lots of doughnuts and doughnut holes found with a foreign strand. Consumers in Georgia and South Carolina should discard these products.

    Product
    Krispy Kreme Doughnuts, Glazed Cake, Doughnut Holes, Manufactured under the authority of Krispy Kreme Doughnut Corporation, Winston-Salem, NC 27102.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0200-2018·2017-12-13

    Exactech Vantage Total Ankle Tibial Insert Recalled for Labeling Mismatch

    Exactech is recalling nine Vantage Total Ankle Tibial Inserts due to possible mismatches between inner and outer packaging labels.

    Product
    Vantage Total Ankle Tibial Insert, Fixed Bearing, 7 mm, Left, Size 3. Exactech Inc., Intended for patients with ankle joints damage by severe rheumatoid, post-traumatic, or degenerative arthritis. It is also indicated for revision of failed previous reconstructions where su
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-0440-2018·2017-12-13

    JP's Delicacies Recalls Holi Aioli Lemon Basil Bottles

    JP's Delicacies LLC is recalling 1,344 bottles of Holi Aioli, Lemon Basil, 12oz, due to bulging bottles found during store inspections.

    Product
    Holi Aioli, Lemon Basil 12oz bottle
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-0493-2018·2017-12-13

    Kroger Recalls Comforts FOR BABY Purified Water Due to Mold Complaint

    The Kroger Co. is recalling Comforts FOR BABY Purified Water with Fluoride Added after a complaint of mold was found in the product.

    Product
    Comforts FOR BABY Purified Water with Flouride Added. 1 GAL (3.78 L) DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Food)·F-0450-2018·2017-12-13

    Krispy Kreme Glazed Mini Crullers Recalled for Foreign Matter

    Krispy Kreme is recalling Glazed Mini Crullers because a foreign strand was found in the product. The recall affects 4,041 boxes sold in Georgia and South Carolina.

    Product
    Krispy Kreme Doughnuts, Glazed Mini Crullers, Net Wt. 10 oz, Manufactured under the authority of Krispy Kreme Doughnut Corporation, Winston-Salem, NC 27102.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0435-2018·2017-12-13

    Donkey Salsa Recalls Salsa Not Hot Due to Plastic Contamination

    Donkey Salsa is recalling Salsa Not Hot 15 oz jars because they may contain pieces of plastic. The product was distributed in New York.

    Product
    SALSA NOT HOT Net Wt. 15 oz (426G)
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0199-2018·2017-12-13

    DeRoyal Surgical Kits Recalled for Incorrect Expiration Date on Prep Pads

    DeRoyal is recalling sterile custom surgical kits containing Medline Aplicare Povidone Iodine Prep Pads due to incorrect expiration dates.

    Product
    DeRoyal Sterile Custom kits containing Medline Aplicare Povidone Iodine Prep Pads: a) Incision and Drainage Tray, REF 47-763.04 b) Incision and Drainage Tray, REF 47-763.06 c) Incision and Drainage Tray, REF 47-763.07 d) Cricothyreotomy Ambulance Kit, REF 89-6752.01 e) Incis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0448-2018·2017-12-13

    Krispy Kreme Original Glazed Doughnuts Recalled for Foreign Matter

    Krispy Kreme is recalling Original Glazed Doughnuts because a foreign matter strand was found on the product. The recall affects 4,041 boxes and containers distributed in Georgia and South Carolina.

    Product
    Krispy Kreme Doughnuts, Original Glazed Doughnuts, Net Wt. 9.4oz (half dozen) and Net Wt. 18.7oz (one dozen), Manufactured under the authority of Krispy Kreme Doughnut Corporation, Winston-Salem, NC 27102.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0211-2018·2017-12-13

    Biosense Webster Recalls PENTARAY NAV High-Density Mapping Catheters

    Biosense Webster is recalling PENTARAY NAV High-Density Mapping Catheters because the instructions for use were updated to indicate they should not be used in patients with prosthetic valves.

    Product
    PENTARAY NAV High-Density Mapping Catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0212-2018·2017-12-13

    Biosense Webster Recalls PENTARAY NAV Mapping Catheters Due to Labeling Update

    Biosense Webster is recalling 73,796 PENTARAY NAV High-Density Mapping Catheters to update contraindication language in the Instructions For Use regarding prosthetic valves.

    Product
    PENTARAY NAV High-Density Mapping Catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0107-2018·2017-12-13

    Elite Laboratories Recalls Isradapine Capsules Due to Impurity Failures

    Elite Laboratories Inc. is recalling 1,264 bottles of Isradapine Capsules USP 2.5 mg in New York due to failed impurities and degradation specifications.

    Product
    Isradapine Capsules USP 2.5 mg, 100-count bottles, Rx only, Manufactured by: Elite Laboratories, Inc. Northvale, NJ 07647, NDC 42806-263-01, UPC 342806263013
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0206-2018·2017-12-13

    Novo Nordisk Recalls Dial-A-Dose Insulin Pen Cartridge Holders

    Novo Nordisk is recalling specific batches of Dial-A-Dose insulin pen cartridge holders because they may crack or break when exposed to certain cleaning agents.

    Product
    Dial-A-Dose Insulin Delivery Device (Pen-Injector) cartridge holders Product Usage: The NovoPen Echo¿ is a re-usable pen injector for single patient use by diabetics for the self injection of a desired dose of insulin. The pen injector uses Penfill 3 mL cartridge of NovoLog¿,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0590-2018·2017-12-13

    C.R. Bard Recalls Arctic Sun ArcticGel Pads Due to Labeling Error

    C.R. Bard is recalling 128 units of Arctic Sun ArcticGel Pads - Medium because the product box displays an incorrect reference number.

    Product
    Arctic Sun ArcticGel Pads - Medium, Product Code 317-07
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-0198-2018·2017-12-13

    BD Phoenix AP Instrument Recalled for Potential Robot Arm Movement

    Becton Dickinson & Co. is recalling seven BD Phoenix AP instruments due to a potential for unexpected robot arm movement.

    Product
    BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is intended to standardize ID broth tube inoculum, add AST indicator to the AST broth tube and transfer an aliquot of ID broth to AST broth tubes, as required for
    Category
    Medical Device
    Distribution
    3 states
  • SevereNHTSA·17V798000·2017-12-12

    Micro Bird G5 School Bus Recall for Roof Crush Risk

    Micro Bird is recalling 2006-2017 G5 school buses because the roof may crush excessively in a rollover, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V797000·2017-12-12

    Newmar Recalls 2018 Bay Star Motorhomes for Lighting Defects

    Newmar is recalling 194 2018 Bay Star and Bay Star Sport motorhomes because front side marker lights may be disconnected and low beams may fail to illuminate with high beams.

    Product
    NEWMAR — NEWMAR BAY STAR SPORT, BAY STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·128-2017·2017-12-12

    Santa Fe Importers Recalls Pork Salami Due to Metal Shavings

    Santa Fe Importers, Inc. is recalling approximately 143 pounds of Marisa Premium Quality Genoa Salami Italian Brand due to possible contamination with metal shavings.

    Product
    Santa Fe Importers, Inc. — Santa Fe Importers, Inc. Recalls Ready-To-Eat Pork Products due to Possible Extraneous Material Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·17V796000·2017-12-11

    Aston Martin Recalls 3,493 Vehicles for Transmission Park Pawl Defect

    Aston Martin is recalling 3,493 vehicles because a communication error may prevent the transmission park pawl from engaging, increasing the risk of the vehicle rolling unexpectedly.

    Product
    ASTON MARTIN — ASTON MARTIN VIRAGE, DBS, DB9, RAPIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V788000·2017-12-11

    Ford Ranger Recall: Passenger Air Bag Inflator Rupture Risk

    Ford is recalling 2004-2006 Ranger trucks because the passenger air bag inflator may rupture during deployment, sending metal fragments into the vehicle.

    Product
    FORD — FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V787000·2017-12-11

    Ford Ranger Recall: Driver Air Bag Inflator Rupture Risk

    Ford is recalling 2004-2006 Ranger trucks to replace driver air bag inflators that may rupture during deployment, posing a risk of serious injury.

    Product
    FORD — FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V795000·2017-12-11

    Aston Martin Recalls DB9 and DBS Vehicles for Battery Cable Fire Risk

    Aston Martin is recalling 2005-2009 DB9 and DBS vehicles because the battery supply cable may be damaged by the driver seat, creating a fire risk.

    Product
    ASTON MARTIN — ASTON MARTIN DB9, DBS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18057·2017-12-11

    Ravin Crossbows Recalls Arrow Nocks Due to Injury Hazard

    Ravin Crossbows is recalling approximately 220,000 white plastic arrow nocks because they may malfunction, posing an injury hazard to users.

    Product
    Ravin arrow nocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V792000·2017-12-11

    Navistar Recalls International Trucks Due to Fire Extinguisher Defect

    Navistar is recalling specific International trucks because the installed fire extinguishers may clog, require excessive force to activate, or detach, potentially causing injury or failing to suppress a fire.

    Product
    INTERNATIONAL — INTERNATIONAL DURASTAR, 9100I, 4900, 4700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V791000·2017-12-08

    JH Global Recalls 2017 Star EV Sport 4+2 for Steering Defect

    JH Global is recalling 2017 Star EV Sport 4+2 vehicles because a casting problem may cause the tie rod to break, resulting in a loss of steering control.

    Product
    STAR EV — STAR EV SPORT 4+2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V785000·2017-12-08

    KZRV Recalls 2014-2015 Durango Gold Trailers Due to Step Rivet Failure

    KZRV is recalling 2014-2015 Durango Gold recreational trailers because quad entry step rivets may shear, causing steps to fail and increasing the risk of falls and injury.

    Product
    KZRV — KZRV DURANGO GOLD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V789000·2017-12-08

    Grand Design Recalls 2017-2018 Travel Trailers Due to Tongue Jack Defect

    Grand Design is recalling 2017-2018 Reflection and Imagine travel trailers because a cracked touch pad on the power tongue jack may allow water entry, causing the jack to operate unintentionally.

    Product
    GRAND DESIGN — GRAND DESIGN IMAGINE, REFLECTION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V786000·2017-12-08

    Midwest Recalls Fire Extinguishers in Mercedes-Benz and RAM Vans

    Midwest Automotive Designs is recalling fire extinguishers in certain 2014-2017 Mercedes-Benz Sprinter and 2016-2017 RAM Promaster vans because they may clog or detach.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, RAM SPRINTER 3500, PROMASTER, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18056·2017-12-08

    One Stop Shop Recalls Children's Pajamas for Flammability Violation

    One Stop Shop is recalling about 350 children's pajama sets sold at Foreman Mills because they fail federal flammability standards, posing a burn risk.

    Product
    Children's pajama sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateNHTSA·17V790000·2017-12-08

    Forest River Recalls 2018 Salem and Wildwood Trailers for Incorrect Tire Placards

    Forest River is recalling 2018 Salem and Wildwood recreational trailers because the Federal Placard incorrectly lists the tire size, which could lead to the installation of wrong-sized tires.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18055·2017-12-07

    Westinghouse Portable Inverter Generators Recalled Due to Fire Hazard

    MWE Investments is recalling Westinghouse iGen2500 and iPro2500 portable inverter generators because they can overheat and catch fire. Consumers should stop using the units and contact the company for a free repair.

    Product
    Portable Inverter Generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide

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