The Recall Desk

Archive

February 2017 recalls

436 recalls were announced in February 2017.

What the numbers show

Critical
36
Severe
125
High
176
Moderate
78
Low
21

Of the 436 recalls this month scored against our rubric, 8% are Critical, 29% are Severe.

101–200 of 436

  • ModerateNHTSA·17V106000·2017-02-17

    Keystone Recalls 2017 Dutchmen Coleman Trailers for Incorrect Tire Labeling

    Keystone is recalling 2017 Dutchmen Coleman recreational trailers because the Federal Identification Tag lists incorrect tire and rim sizes, which could lead to improper equipment use.

    Product
    DUTCHMEN — DUTCHMEN COLEMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17088·2017-02-16

    Britax Recalls Strollers Due to Car Seat Fall Hazard

    Britax is recalling B-Agile and BOB Motion strollers because a damaged receiver mount can cause car seats to fall, posing a hazard to infants.

    Product
    Britax B-Agile and BOB Motion Strollers with Click & Go receivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17E009000·2017-02-16

    Hale Fire Pump Pressure Switch Recall for Cold Weather Failure

    Hale Products Inc. is recalling Fire Pump Engagement Pressure Switches that may fail in extremely cold temperatures, potentially delaying water delivery during fires.

    Product
    EQUIPMENT:MECHANICAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V104000·2017-02-16

    Volvo Recalls 2017 Models Due to Air Bag Bolt Failure Risk

    Volvo is recalling 2017 XC90, S90, and V90 Cross Country vehicles because side air bag bolts may break, causing improper deployment in a crash.

    Product
    VOLVO — VOLVO V90CC, S90, XC90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1466-2017·2017-02-15

    Blommer Recalls Cocie White Confectionery Discs Due to Salmonella Risk

    Blommer Chocolate Co. is recalling Cocie High Protein 90 White Confectionery Discs because the product contains milk and buttermilk powders that may be contaminated with Salmonella.

    Product
    Cocie High Protein 90 White Confectionery Discs - MB, NET WT: 40 LBS
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1462-2017·2017-02-15

    Franklin Farms East Recalls All Dairy Blend Due to Salmonella Risk

    Franklin Farms East is recalling 5,050 pounds of All Dairy Blend FFE-9967 because the product may be contaminated with Salmonella.

    Product
    All Dairy Blend FFE-9967: Lot # s 1609214-16, 5,050 pounds, packed in 50# poly lined Kraft paper bags, expiration date April 1st, 2017.
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1437-2017·2017-02-15

    Subco Recalls French Vanilla Pudding for Salmonella Risk

    Subco Foods is recalling Best Choice French Vanilla Instant Pudding & Pie Filling because an ingredient may be contaminated with Salmonella.

    Product
    Best Choice French Vanilla Instant Pudding & Pie Filling, UPC 0 70038 31221 5, Distributed by Associated Wholesale Grocers, INC, 3.4 oz.
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Food)·F-1460-2017·2017-02-15

    Franklin Farms East Recalls Buttermilk Solids Due to Salmonella Risk

    Franklin Farms East is recalling 42,650 pounds of Buttermilk Solids because the product may be contaminated with Salmonella.

    Product
    Buttermilk Solids FFE-8902: Lot # s 1608301-18, 42,650 pounds, packed in 50# poly lined Kraft paper bags, expiration date March 3rd, 2017.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1439-2017·2017-02-15

    Subco Pistachio Pudding Recalled for Possible Salmonella in Milk Ingredient

    Subco Foods is recalling Best Choice Pistachio Instant Pudding & Pie Filling because a milk powder ingredient may be contaminated with Salmonella.

    Product
    Best Choice Pistachio Instant Pudding & Pie Filling, UPC 0 70038 31220 8, 3.4 oz, Distributed by Associated Wholesale Grocers, INC.
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Food)·F-1453-2017·2017-02-15

    Bickel's Recalls Bon Ton Sour Cream and Onion Potato Chips

    Bickel's Snack Foods is voluntarily recalling Bon Ton Sour Cream & Onion potato chips due to milk ingredients from a secondary supplier.

    Product
    Bon Ton-Sour Cream & Onion Flavored Potato Chips sold in 2.75 oz, 1.5 oz. bags
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Devices)·Z-1183-2017·2017-02-15

    Invacare Recalls Bariatric Beds Due to Fire Hazard

    Invacare is recalling Bariatric Beds (BARPKG-IVC 1633) because a quality issue with the junction box may cause sparks and result in a fire.

    Product
    Bariatric Bed - BARPKG-IVC 1633
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1138-2017·2017-02-15

    Carestream DRX-Revolution Mobile X-Ray System Recalled for Brake Failure

    Carestream Health is recalling DRX-Revolution Mobile X-Ray Systems because a complaint alleged the unit could not be stopped when applying the brake, resulting in a crash into an elevator.

    Product
    Carestream DRX-Revolution Mobile X-Ray System, Model DRXR-1, Catalog No. 1019397 (all other countries), Catalog No. 1060177 (China only) -- Carestream Health, Inc. 150 Verona Street, Rochester, NY 14608
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1184-2017·2017-02-15

    Invacare Recalls Bariatric Bed Foot Sections Due to Fire Risk

    Invacare Corporation is recalling 292 bariatric bed foot sections because a quality issue with the junction box may cause sparks and result in a fire.

    Product
    Foot Section - BAR5490IVC
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Food)·F-1456-2017·2017-02-15

    Bickel's Recalls Troyer Sour Cream and Onion Potato Chips

    Bickel's Snack Foods is voluntarily recalling Troyer Sour Cream & Onion Potato Chips due to milk ingredients from a secondary supplier.

    Product
    Troyer- Sour Cream & Onion Flavored Potato Chips sold in 2oz., and 8.5 oz. bags.
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1455-2017·2017-02-15

    Bickel's Potato Chips Recalled Due to Milk Ingredient Supply Issue

    Bickel's Snack Foods is voluntarily recalling Sour Cream & Onion potato chips because they were made with milk ingredients from a secondary supplier.

    Product
    Bickel's Sour Cream & Onion Flavored Potato Chips sold in .75 oz., 2 oz., 7 oz., and 8.5 oz. bags.
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1457-2017·2017-02-15

    Bickel's Recalls Dan Dee Sour Cream and Onion Potato Chips

    Bickel's Snack Foods is voluntarily recalling Dan Dee Sour Cream & Onion potato chips due to potential milk contamination from a secondary supplier.

    Product
    Dan Dee - Sour Cream & Onion Flavored Potato Chips sold in 7/8 oz., 2 oz., and 8.5 oz. bags
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1447-2017·2017-02-15

    Circle U Foods Recalls Taco Seasoning for Potential Glass Inclusion

    Circle U Foods, Inc. is recalling 8 cases of 1.1250 lb Taco Seasoning bags due to a potential glass inclusion. The product was distributed in Texas, Illinois, Kansas, and North Carolina.

    Product
    Circle U Foods, Inc. Product Code: 100002 AF/TV Taco Seasoning Bag Weight: 1.1250 Lbs.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1461-2017·2017-02-15

    Franklin Farms East Recalls Buttermilk Solids Due to Salmonella Risk

    Franklin Farms East is recalling 5,050 pounds of Buttermilk Solids because the product may be contaminated with Salmonella. The affected lots were distributed in Georgia, Pennsylvania, and Alabama.

    Product
    Buttermilk Solids FFE-8906: Lot # s 1609221-22, 5,050 pounds, packed in 50# poly lined Kraft paper bags, expiration date April 1st, 2017.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1448-2017·2017-02-15

    Circle U Foods Recalls Cajun Buttermilk Dressing Due to Glass Inclusion

    Circle U Foods is recalling 29 cases of Cajun Buttermilk Dressing due to potential glass inclusion. The product was distributed in Texas, Illinois, Kansas, and North Carolina.

    Product
    Circle U Foods, Inc. Product Code: 908041 RCC/Cajun Buttermilk Dressing Bag Weight: 0.88 Lbs.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1182-2017·2017-02-15

    Invacare Bariatric Bed Recall Due to Fire Hazard

    Invacare is recalling 411 bariatric beds because the junction box may emit sparks and cause a fire.

    Product
    Bariatric Bed - BAR600IVC
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Food)·F-1458-2017·2017-02-15

    Bickel's Recalls Cabana Sour Cream and Onion Potato Chips

    Bickel's Snack Foods is voluntarily recalling Cabana Sour Cream & Onion potato chips due to potential milk contamination from a secondary supplier.

    Product
    Cabana- Sour Cream & Onion Flavored Potato Chips sold in 5 oz. bags
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1459-2017·2017-02-15

    Bickel's Recalls Key Foods Potato Chips Due to Milk Ingredient Concerns

    Bickel's Snack Foods is voluntarily recalling Key Foods Sour Cream & Onion Potato Chips because they were made with milk ingredients from a secondary supplier.

    Product
    Key Foods - Sour Cream & Onion Flavored Potato Chips sold in 6 oz. bags
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1454-2017·2017-02-15

    Bickel's Recalls Seyfert Sour Cream and Onion Potato Chips

    Bickel's Snack Foods is voluntarily recalling Seyfert Sour Cream & Onion potato chips due to milk ingredients from a secondary supplier.

    Product
    Seyfert-Sour Cream & Onion Flavored Potato Chips sold in 2 oz., 5 oz., 8.5 oz. bags
    Category
    Food
    Distribution
    7 states
  • SevereNHTSA·17V103000·2017-02-15

    PACCAR Recalls Kenworth and Peterbilt Trucks Due to Fuel Leak Risk

    PACCAR is recalling 2015-2018 Kenworth and 2017-2018 Peterbilt trucks because plastic fuel tee fittings may leak fuel, increasing the risk of fire.

    Product
    KENWORTH — KENWORTH, PETERBILT K370, 567, 579, T680
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V102000·2017-02-15

    Prevost Recalls 2017 Motor Coaches Due to Steering Arm Lever Defect

    Prevost is recalling 2017 H3-45 and X3-45 motor coaches because incorrectly forged steering arm levers may crack and fail, increasing crash risk.

    Product
    PREVOST — PREVOST H3-45, X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1185-2017·2017-02-15

    Invacare Bariatric Bed Junction Box Recalled for Fire Risk

    Invacare is recalling 161 bariatric bed junction boxes due to a quality issue that may cause sparks and result in a fire.

    Product
    Junction Box - 1104343 and 1193560
    Category
    Medical Device
    Distribution
    37 states
  • HighFDA (Food)·F-1438-2017·2017-02-15

    Subco Recalls Lemon Pudding for Possible Salmonella in Milk Ingredient

    Subco Foods of Wisconsin is recalling Best Choice and Always Save Lemon Instant Pudding & Pie Filling because a milk ingredient may contain Salmonella.

    Product
    Best Choice Lemon Instant Pudding & Pie Filling UPC 0 70038 31222 2, 3.4 oz, Distributed by Associated Wholesale Grocers, INC, and Always Save Lemon Instant Pudding & Pie Filling; UPC 0 70038 31215 4, 3.4 oz,. Distributed by Associated Wholesale Grocers, INC .
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-1180-2017·2017-02-15

    Merge RadSuite software recalled due to incorrect pixel value data

    Merge Healthcare is recalling RadSuite software version V8.30.7.8 because incorrect pixel values may lead to patient injury or delayed diagnosis.

    Product
    Merge RadSuite software. The firm name on the label is Merge Healthcare, Hartland, WI.
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-0927-2017·2017-02-15

    Bayer Recalls Medrad Intego PET Infusion System Pumps

    Bayer is recalling Medrad Intego PET Infusion System pumps because the administration sets may produce particulates in radiopharmaceutical vials.

    Product
    MEDRAD Intego PET Infusion System - Pump Intended to deliver accurate doses of Fluoredeoxyglucose or F-Sodium Fluoride and commonly used flushing solutions to patients during molecular imaging (nuclear medicine) diagnostic procedures. It is also intended to provide effective rad
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1449-2017·2017-02-15

    Circle U Foods Recalls Bayou Seasoning Due to Potential Glass Inclusion

    Circle U Foods, Inc. is recalling 8 cases of Razzoo's/Bayou Seasoning due to a potential glass inclusion hazard.

    Product
    Circle U Foods, Inc. Product Code: 900012 Razzoo's/Bayou Seasoning, RCC/Bayou Seasoning Bag Weight: 0.29 Lbs.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1440-2017·2017-02-15

    Dannon Dairy Drink Recalled for Incorrect Walnut Allergen Labeling

    Dannon is recalling specific bottles of Dairy Drink Nut and Cereal because the label incorrectly lists walnut as an ingredient and allergen, while the product actually contains pecan.

    Product
    DANONE¿ DAIRY DRINK NUT AND CEREAL 7.7 FL OZ (229mL) bottles, UPC 36632 01421
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-1137-2017·2017-02-15

    AngioDynamics Recalls Celerity ECG Cable Accessory Packs Due to Soldering Defect

    AngioDynamics is recalling Celerity ECG Cable Accessory Packs because the ECG clip cable may not be soldered correctly, potentially preventing the device from conducting ECG signals.

    Product
    Celerity ECG Cable Accessory Pack, STERILE, Rx ONLY - distributed under the following labels: (a) angiodynamics UPN/Product No. H787471431, REF/Catalog No. 47-143 -- Legal Manufacturer: AngioDynamics, Inc. 10 Glens Falls Technical Park, Glens Falls, NY 12801; and (b) medCOMP UPN/
    Category
    Medical Device
    Distribution
    19 states
  • HighFDA (Food)·F-1452-2017·2017-02-15

    Taylor Farms Rotini Pasta Salad Recalled for Undeclared Wheat Allergen

    Taylor Farms is recalling 10 oz. Rotini Pasta Salad containers because the label incorrectly identifies the product as mustard potato salad, failing to declare the wheat allergen.

    Product
    Fresh Foods Market Delicatessen Rotini Pasta Salad; Net Wt. 10 oz . (283g) Clamshell package. UPC Code: WO2017019 Perishable; Keep Refrigerated; Distributed by The Kroger Col., Cincinnati, OH
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1443-2017·2017-02-15

    Dawson Foods Recalls Creamy White Frosting Mix for Salmonella Risk

    Dawson Foods is voluntarily recalling Creamy White Frosting Mix and Kustard Kwik Mix because a supplier recalled dried milk for potential Salmonella contamination.

    Product
    Dawson Foods Inc. Creamy White Frosting Mix , 5 Lb Bags, 6 5Lb bags per case Creamy White, Ambient Storage
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1149-2017·2017-02-15

    Stryker Leibinger Recalls Surgical Drainage Accessories Due to Sterility Labeling Error

    Stryker Leibinger is recalling QUINTUBE Monitor Packs and SPG Bulb Drain Systems because non-sterile products were incorrectly labeled as sterile.

    Product
    QUINTUBE Monitor Pack (5 tubes/pk, 24 pk/case) (Non-Sterile) SPG Bulb Drain System, 4mm Flat w/Center Holes (Sterile) Accessories to TLS Surgical Drainage System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1176-2017·2017-02-15

    Merge PACS Software Recalled for Potential Incorrect Patient Image Display

    Merge Healthcare is recalling Merge PACS software version 7.0.1 because it may display incorrect patient images, potentially delaying diagnosis or treatment.

    Product
    Merge PACS software. The firm name on the label is Merge Healthcare, Hartland, WI.
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Food)·F-1450-2017·2017-02-15

    Circle U Foods Recalls Deli Sauce Seasoning Due to Glass Inclusion

    Circle U Foods is recalling 12 cases of Elmer's Deli Sauce Seasoning due to a potential glass inclusion. The product was distributed in Texas, Illinois, Kansas, and North Carolina.

    Product
    Circle U Foods, Inc. Product Code: 211013 NPP/Elmer's Deli Sauce Seasoning Pounds Per Bag/Box: 25.00 Lbs.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1436-2017·2017-02-15

    Subco Foods Recalls Vanilla Pudding Due to Salmonella Risk

    Subco Foods of Wisconsin is recalling specific vanilla pudding products because an ingredient, high heat nonfat dry milk powder, may be contaminated with Salmonella.

    Product
    Bakers Corner Vanilla Instant Pudding & Pie Filling, UPC 0 41498 15253 6 Distributed by ALDI; Best Choice Vanilla pudding UPC 0 70038 31218 5 Distributed by Associated Wholesale Grocers, INC(AWG) and Always Save Vanilla Pudding, UPC 0 70038 31200 0, Distributed by Associated Wh
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-1144-2017·2017-02-15

    Physio-Control Recalls LIFEPAK 15 Defibrillators with Erroneous CO2 Readings

    Physio-Control is recalling LIFEPAK 15 Monitor/Defibrillators with End-Tidal CO2 options because the CO2 reading may intermittently display an incorrect value of XXX.

    Product
    LIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option. Intended for use by trained medical personnel in out-of-doors and indoor emergency care settings within the environmental conditions specified in the Operating Instructions.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1178-2017·2017-02-15

    Boston Scientific Recalls EMBLEM S-ICD Programmer Model 3200

    Boston Scientific is recalling 4,500 EMBLEM S-ICD Programmer Model 3200 units due to a potential risk of radio frequency interference causing unintended commands during in-clinic sessions.

    Product
    Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1142-2017·2017-02-15

    Merge Healthcare Recalls Eye Station Imaging Devices Due to Capture Failures

    Merge Healthcare is recalling 182 Eye Station capture stations because they may fail to capture eye images as intended, posing a risk to patient health.

    Product
    Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager distributed by Ophthalmic Imaging Systems (OIS). Model number 136 T1700 Capture Stations & 46 T5810 Capture Stations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1148-2017·2017-02-15

    AtriCure Recalls AtriClip LAA Exclusion System Due to Jaw Breakage

    AtriCure is recalling 464 AtriClip LAA Exclusion System devices because a complaint was received regarding the PRO2 jaw breaking prior to surgery.

    Product
    AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A single PRO2 device is packaged in a conventional thermoformed polyethylene terephthalate glycol (PETG) tray with a Tyvek¿ lid. A single-walled non-corrugated box completes the single unit package. Six (6) s
    Category
    Medical Device
    Distribution
    31 states
  • HighFDA (Food)·F-1445-2017·2017-02-15

    Annie's Kitchen Vegetable Soup Recalled for Undeclared Wheat Allergen

    Annie's Kitchen is recalling Vegetable Soup because the noodle ingredient contains wheat, which was not declared on the label.

    Product
    Vegetable Soup; Annie's Kitchen; 2966 Stumptown Rd, Ronks, PA 17572 16 FL OZ
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1451-2017·2017-02-15

    Marich Chocolate Caramel Heart Recalled for Unlabeled Almond Allergen

    Marich Confectionery is recalling Chocolate Caramel Hearts because some boxes contained Triple Chocolate Toffee with almonds, which are not listed on the Caramel Heart label.

    Product
    MARICH Premium Chocolates; Chocolate Caramel Heart; Our delicious caramel hearts in rich milk and dark chocolate; Net Wt 4.25 oz. (120g) UPC 797817-44440-9
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1435-2017·2017-02-15

    Dutch Valley Recalls Cappuccino Snack Mix Due to Salmonella Risk

    Dutch Valley Food Distributors is recalling Cappuccino Snack Mix because it may be contaminated with Salmonella. The recall affects 157 cases distributed across 22 states.

    Product
    Cappuccino Snack Mix Lot code: 20161027; Best By: 05/25/17 Net Wt: 10 lb (2-5lb bags)
    Category
    Food
    Distribution
    22 states
  • HighFDA (Devices)·Z-1177-2017·2017-02-15

    Teleflex Recalls Sheridan Cuffed Tracheal Tubes Due to Labeling Inconsistency

    Teleflex Medical is recalling Sheridan cuffed tracheal tubes because some units are labeled with incorrect sizes, potentially leading to improper airway management.

    Product
    Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A tracheal tube is inserted into a patients mouth or nose for airway management
    Category
    Medical Device
    Distribution
    38 states
  • ModerateFDA (Devices)·Z-1150-2017·2017-02-15

    Stryker Leibinger Recalls Non-Sterile Medpor Implant Sizer Sets Due to Labeling Error

    Stryker Leibinger is recalling specific non-sterile Medpor implant sizer sets because they were incorrectly labeled as sterile. The recall covers 619 units distributed in the US and several international countries.

    Product
    9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design M Malar Sizer Set (Silicone, Non-Sterile) 9952 Extended Contoured, Malar Sizer Set (Silicone, Non-Sterile) 85000 Petite Nasal Dorsum Sizer Set (Silicone, Non-Sterile) Accessories to Medpor Implants
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1181-2017·2017-02-15

    Ortho VITROS FS Calibrator 1 Recalled Due to Calibration Failure

    Ortho-Clinical Diagnostics is recalling VITROS FS Calibrator 1, Lot 91461, because it cannot calibrate dLDL reagents when used with specific Assay Data Disk versions.

    Product
    VITROS Chemistry Products FS Calibrator 1, REF 680 1873 12 x 3 mL, Rx ONLY, IVD; used in conjunction with VITROS Chemistry Products Calibrator Kits to calibrate VITROS 5,1 FS/4600 Chemistry and integrated Systems. --- Ortho-Clinical Diagnostics, Inc. Rochester, NY 14626 --- Ortho
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0469-2017·2017-02-15

    VistaPharm Recalls Potassium Chloride Oral Solution Due to Cup Leakage

    VistaPharm is recalling 13,609 cases of Potassium Chloride Oral Solution because the unit dose cups may leak at the seal.

    Product
    Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50 unit dose cups per case (NDC 66689-047-50), Rx only, Xact Dose, Manufactured by VistaPharm, Largo, FL 33771.
    Category
    Drug
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-1141-2017·2017-02-15

    Siemens Dimension Vista Ammonia Flex Reagent Cartridge Recall

    Siemens is recalling specific lots of Dimension Vista Ammonia Flex reagent cartridges because they may not meet the 60-day calibration interval claim, potentially resulting in abnormal assay results.

    Product
    Dimension Vista¿ Ammonia Flex¿ reagent cartridge / AMM Dimension: The AMM method is an in vitro diagnostic test for the quantitative measurement of ammonia in human plasma on the Dimension clinical chemistry system. Ammonia measurements are used in the diagnosis and treatment of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1139-2017·2017-02-15

    Encore Medical Recalls Empowr PS Knee Tibial Inserts Due to Missing Feature

    Encore Medical is recalling 24 Empowr PS Knee Tibial Inserts because they are missing the impaction slot feature.

    Product
    Empowr PS Knee Tibial Insert; Model 343-14-709 The EMPOWR PS tibial insert are made from Highly Cross-Linked Vitamin E (HXL VE) UHMWPE. The tibial insert implants are intended to mate with tibial base implants.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1179-2017·2017-02-15

    Ortho-Clinical VITROS UPRO Slides Recalled for Variable Urine Protein Results

    Ortho-Clinical Diagnostics is recalling VITROS UPRO Slides because they may produce variable urine protein results.

    Product
    VITROS Chemistry Products UPRO Slides, UPN 10758750000593, Product Usage: Quantitative measurement of total protein concentration in urine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1140-2017·2017-02-15

    Siemens Dimension Ammonia Reagent Cartridges Recalled for Calibration Issues

    Siemens Healthcare Diagnostics is recalling specific lots of Dimension Ammonia Flex reagent cartridges because they may not meet the 60-day calibration interval claim, potentially leading to abnormal assay results.

    Product
    Dimension¿ Ammonia Flex¿ reagent cartridge / AMM Dimension: The AMM method is an in vitro diagnostic test for the quantitative measurement of ammonia in human plasma on the Dimension clinical chemistry system. Ammonia measurements are used in the diagnosis and treatment of seve
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1143-2017·2017-02-15

    Physio-Control Recalls LIFEPAK 12 Defibrillators with Erratic CO2 Readings

    Physio-Control is recalling LIFEPAK 12 Defibrillators because the End-Tidal CO2 reading may intermittently display an invalid value of XXX during operation.

    Product
    LIFEPAK 12 Defibrillator/Monitor with End-Tidal CO2 option. The device is used in various areas of the hospital such as critical areas (emergency departments, critical care, operating room, etc.) and general duty floors (e.g. medical/surgical). The device is also used for
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1151-2017·2017-02-15

    Vertebral Technologies Recalls InterFuse Tail Traction Tool Due to Fit Issues

    Vertebral Technologies is recalling 63 InterFuse Tail Traction Tools because they may not fit properly with the InterFuse T implant.

    Product
    InterFuse Tail Traction Tool, Part Number 9116. The InterFuse Tail Traction Tool is an optional Class I non-sterile reusable instrument that can be used to assist with module locking of the InterFuse S or InterFuse T implant system. The system has a modular design to allow th
    Category
    Medical Device
    Distribution
    11 states
  • LowFDA (Drugs)·D-0471-2017·2017-02-15

    Apotex Recalls Aripiprazole Tablets Due to Potential Potency Issues

    Apotex Inc. is recalling 67,946 bottles of 2 mg Aripiprazole tablets because the product may not meet specifications throughout its shelf life.

    Product
    Aripiprazole Tablets, 2 mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9; Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-3075-3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·013-2017·2017-02-15

    Century Packing Recalls Chicken Sausage Products Due to Undeclared MSG

    Century Packing Corp. is recalling approximately 999,419 pounds of chicken sausage products because they contain undeclared monosodium glutamate (MSG).

    Product
    Century Packing Corp. — Century Packing Corp. Recalls Chicken Sausage Products Due To Misbranding
    Category
    Food
    Distribution
    2 states
  • LowFDA (Drugs)·D-0470-2017·2017-02-15

    Aurobindo Recalls Discolored Pantoprazole Sodium Injection Vials

    Aurobindo Pharma USA Inc is recalling 29,800 vials of Pantoprazole Sodium for Injection due to discoloration. The affected vials contain powder with a yellowish-brownish appearance.

    Product
    PANTOPRAZOLE SODIUM — PANTOPRAZOLE SODIUM (PANTOPRAZOLE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1146-2017·2017-02-15

    Thayer MiniSpacer MDI Adapter Recalled for Incorrect Labeling

    Thayer Medical Corporation is recalling 2,550 MiniSpacer MDI adapters because the insert and case labels incorrectly state the connection size.

    Product
    Thayer MiniSpacer Dual Spray MDI Adapter Counter Incrementing Actuator with 15mm O.D./I.D. Connections, Reference no. 1543A. The 15 mm Dual Spray MiniSpacer with Counter Incrementing Actuator is a non-sterile, single-use item, intended to dispense aerosolized medication into a b
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1145-2017·2017-02-15

    FDA Recalls Hotline Blood and Fluid Warmers for Incorrect Language Labeling

    Smiths Medical ASD, Inc. is recalling 33 Hotline Blood and Fluid Warmers distributed to Finland because they included Greek and Danish labeling instead of the required Finnish labeling.

    Product
    HOTLINE Blood and Fluid Warmer, Mole l HL-90. Designed for use with the Hotline Fluid Warming Set (L-80, L-70 and L-70N) to warm blood and intravenous (I.V.) fluids and deliver them to the patient's intravenous access site at normothermic temperatures under gravity flow conditio
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·17V097000·2017-02-14

    Chrysler Recalls 2014-2017 AWD Vehicles for Driveshaft Bolt Issue

    Chrysler is recalling 2014-2017 Dodge Charger and Chrysler 300 AWD vehicles because front driveshaft bolts may loosen, potentially causing a loss of motive power and increasing crash risk.

    Product
    DODGE — DODGE, CHRYSLER CHARGER, 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V096000·2017-02-14

    Thor Motor Coach Recalls 2014-2016 Motorhomes for Wiper Defect

    Thor Motor Coach is recalling 2,483 motorhomes because improperly installed windshield wipers may fail, reducing visibility and increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR PALAZZO, TUSCANY, TUSCANY XTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V095000·2017-02-13

    Forest River Recalls 2017 Palomino Columbus RVs Due to Propane Hose Defect

    Forest River is recalling 2017 Palomino Columbus recreational vehicles equipped with an optional generator package because the liquid propane supply hose may be too small, posing a fire or explosion risk.

    Product
    PALOMINO — PALOMINO COLUMBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17087·2017-02-13

    Target Recalls Threshold Patio Benches Due to Fall Hazard

    Target is recalling about 1,300 Threshold patio benches because they can collapse while in use, posing a fall hazard.

    Product
    Threshold patio benches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·012-2017·2017-02-11

    Taylor Farms Recalls Chicken and Pork Salads Due to Listeria Risk

    Taylor Farms is recalling specific chicken and pork salad products due to potential Listeria monocytogenes contamination. Consumers should discard or return these items.

    Product
    Taylor Farm - Pacific — Taylor Farms Recalls Chicken and Pork Salad Products Due To Possible Listeria Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·17V094000·2017-02-10

    Mercedes-Benz Recalls 2015 Sprinter Vans for Driveshaft Defect

    Daimler Vans USA is recalling 2015 Mercedes-Benz Sprinter 2500 and 3500 vehicles because a missing driveshaft catch strap could allow the driveshaft to strike the fuel tank, increasing fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V092000·2017-02-10

    Mercedes-Benz Recalls 2015 Sprinter Vans for Fuel Tank Defect

    Daimler Vans USA is recalling 2015 Mercedes-Benz Sprinter 2500 and 3500 vehicles because missing protective parts may allow fuel leaks and fire risks.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V093000·2017-02-10

    Mercedes-Benz and Freightliner Sprinter Vans Recalled for Air Bag Defect

    Daimler Vans USA is recalling 2013-2016 Sprinter vans because the air bag control unit may fail to function after a first impact, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·17V091000·2017-02-10

    Heartland Recalls 2017 Sundance Trailers for Missing Weight Rating Label

    Heartland is recalling 2017 Sundance recreational trailers because the Federal Certification label may be missing the Gross Vehicle Weight Rating, which could lead to overloading.

    Product
    HEARTLAND — HEARTLAND SUNDANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V088000·2017-02-09

    BMW Recalls 2014-2017 i3 REx Vehicles for Fuel Vapor Leak Risk

    BMW is recalling 2014-2017 i3 REx hybrid vehicles because a fuel tank vent line may rub against a battery cable, causing a fuel vapor leak that increases fire risk.

    Product
    BMW — BMW I3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V084000·2017-02-09

    Jaguar Recalls 2017 XF Models Due to Fuel Line Fire Risk

    Jaguar is recalling 2017 XF vehicles because a cracked left inner sill panel could cause fuel lines to rupture in a crash, increasing fire risk.

    Product
    JAGUAR — JAGUAR XF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V082000·2017-02-09

    Mazda Recalls 2010-2011 Models for Seat Lifter Defect

    Mazda is recalling 2010-2011 Mazda2, Mazda3, and Mazdaspeed3 vehicles because seat height adjustment links may break, potentially compromising the driver's position and increasing crash risk.

    Product
    MAZDA — MAZDA MAZDA2, MAZDA3, MAZDASPEED3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V085000·2017-02-09

    Suzuki Recalls 2009-2013 Grand Vitara Manual Transmission Vehicles

    Suzuki is recalling 2009-2013 Grand Vitara vehicles with manual transmissions because the gear shift rear shaft may break, preventing gear changes and increasing crash risk.

    Product
    SUZUKI — SUZUKI GRAND VITARA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17084·2017-02-09

    Feld Entertainment Recalls Light-Spinner Toy Wands Due to Injury Hazard

    Feld Entertainment is recalling light-spinner toy wands sold at Disney shows because a top component can detach, exposing a metal rod that poses an injury risk to young children.

    Product
    Light-spinner toy wands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V087000·2017-02-09

    BMW Recalls 2014 X1 Models for Battery Cable Connection Defect

    BMW is recalling 2014 X1 vehicles because battery positive cables may develop high resistance, potentially causing engine stalls and increasing crash risk.

    Product
    BMW — BMW X1 SAV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1383-2017·2017-02-08

    Del Dee Foods Recalls Organic Pea Protein Due to Salmonella

    Del Dee Foods is withdrawing a specific lot of Organic Pea Protein after salmonella was detected in pre-consumer samples.

    Product
    Hemp & Grain Co., Organic Pea Protein 80%, Net Weight 44.1 lbs. Paper bags, 36 paper bags/pallet.
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1394-2017·2017-02-08

    Houdini Blue Cheese Twists Recalled for Potential Salmonella Contamination

    Houdini Inc. is recalling The Executive with Houdini Blue Cheese Twists due to potential Salmonella contamination. The product was distributed nationwide, including Puerto Rico.

    Product
    The Executive with Houdini Blue Cheese Twists, 7 ounces COM 659 SKU# 54002-3, SKU#54087-0
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1388-2017·2017-02-08

    Houdini Fabric Gift Basket Recalled for Potential Salmonella Contamination

    Houdini Inc. is recalling 2,496 fabric gift baskets due to potential Salmonella contamination. The products were distributed nationwide, including Puerto Rico.

    Product
    Houdini Fabric gift basket, Item No. 1072552
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1372-2017·2017-02-08

    King's Pastry Recalls Cappuccino Carnival Cake for Undeclared Hazelnut

    King's Pastry is recalling frozen Cappuccino Carnival Cakes because the product contains undeclared hazelnut and/or tree nuts, posing a risk to consumers with allergies.

    Product
    Cappuccino Carnival Cake (12"x 16"), 2 kg. Frozen Product Code: 10081 UPC: 1068596110814
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1389-2017·2017-02-08

    Houdini Wooden Centerpiece Gift Baskets Recalled for Salmonella Risk

    Houdini Inc. is recalling 2,080 Wooden Centerpiece gift baskets due to potential Salmonella contamination. The products were distributed nationwide, including Puerto Rico.

    Product
    Wooden Centerpiece gift basket, Item No. 1080571
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1398-2017·2017-02-08

    Houdini Inc. Recalls Bodega de San Antonio Sangria Due to Salmonella Risk

    Houdini Inc. is recalling Bodega de San Antonio Sangria Traditional Basket #298 due to potential Salmonella contamination. The product was distributed nationwide, including Puerto Rico.

    Product
    Bodega de San Antonio Sangria Traditional Basket #298
    Category
    Food
    Distribution
    Distributed nationwide

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