The Recall Desk

Archive

January 2015 recalls

327 recalls were announced in January 2015.

What the numbers show

Critical
23
Severe
124
High
114
Moderate
53
Low
13

Of the 327 recalls this month scored against our rubric, 7% are Critical, 38% are Severe.

1–100 of 327

  • CriticalUSDA FSIS·026-2015·2015-01-30

    Clemens Food Group Recalls Pork Ribs for Undeclared Peanut Allergen

    Clemens Food Group is recalling approximately 42 pounds of uncooked pork rib products due to misbranding and an undeclared peanut allergen.

    Product
    Clemens Food Group, LLC — Pennsylvania Firm Recalls Pork Rib Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    2 states
  • CriticalUSDA FSIS·027-2015·2015-01-30

    El Toro Cooked Pork Products Recalled for Undeclared Peanut Allergen

    El Toro Meat Packing Inc. is recalling cooked pork products because they contain undeclared peanuts, a known allergen.

    Product
    El Toro Meat Packing Inc — Florida Firm Recalls Cooked Pork Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·15V049000·2015-01-30

    Heartland Recalls 2015 RVs Due to Axle Placement and Weight Distribution Issues

    Heartland is recalling specific 2015 Big Country, Big Horn, and Landmark 365 recreational vehicles because axles may be placed too far forward, causing improper weight distribution and poor handling.

    Product
    HEARTLAND — HEARTLAND LANDMARK 365, BIG COUNTRY, BIG HORN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·024-2015·2015-01-30

    Great Lakes Smoked Meats Recalls Salami Due To Temperature Abuse

    Great Lakes Smoked Meats is recalling smoked salami that may have experienced temperature abuse and contain Clostridium perfringens.

    Product
    Ohio Firm Recalls Salami Products Due To Possible Temperature Abuse
    Category
    Food
    Distribution
    4 states
  • SevereUSDA FSIS·025-2015·2015-01-30

    Hawkins Inc. Recalls Pork Products Produced Without Inspection

    Hawkins, Inc. is recalling approximately 529 pounds of dehydrated pork stock and broth produced without the benefit of full inspection.

    Product
    Minnesota Firm Recalls Pork Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V051000·2015-01-30

    PACCAR Recalls 2015 Peterbilt and Kenworth Trucks for Brake Caliper Bolt Issue

    PACCAR is recalling 106 model year 2015 Peterbilt and Kenworth trucks because brake caliper bolts may not be properly torqued, which could reduce braking effectiveness.

    Product
    PETERBILT — PETERBILT, KENWORTH 210, K370, 320, K270
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V052000·2015-01-30

    All Wheel Drive Recalls One 2011 Ford F-550 Truck for Fire Risk

    All Wheel Drive Equipment Mfg. is recalling one 2011 Ford F-550 truck because a PTO pressure switch may leak oil onto the exhaust, increasing fire risk.

    Product
    FORD — FORD F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·023-2015·2015-01-29

    Korean Farm Recalls Chicken Stew Products Lacking Import Inspection

    Korean Farm Inc. is recalling approximately 14,610 pounds of chicken stew products produced in the Republic of Korea that were not presented for U.S. import inspection.

    Product
    California Firm Recalls Chicken Stew Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    9 states
  • HighCPSC·15065·2015-01-29

    Sunbeam Recalls Holmes Oil-Filled Heaters Due to Scald Hazard

    Sunbeam is recalling Holmes oil-filled heaters because they can spray heated oil, posing a scald hazard. No injuries have been reported.

    Product
    Oil-Filled Heater
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0357-2015·2015-01-28

    Walgreens Recalls Ceftriaxone Infusions Due to Sterility Concerns

    Walgreens Infusion Services is recalling ceftriaxone in normal saline due to a lack of sterility assurance. The products were distributed in six states.

    Product
    Ceftriaxone various strengths in normal saline
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0347-2015·2015-01-28

    Walgreens Recalls Ertapenem Infusion Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling Ertapenem in normal saline bags due to a lack of sterility assurance. The products were distributed in six states.

    Product
    Ertapenem various strength in normal saline bags
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0360-2015·2015-01-28

    Walgreens Recalls Tigecycline Infusions Due to Sterility Concerns

    Walgreens Infusion Services is recalling Tigecycline in normal saline due to a lack of sterility assurance. The products were distributed in six southern states.

    Product
    Tigecycline various strengths in normal saline
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0349-2015·2015-01-28

    Walgreens Recalls Vancomycin Infusion Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling Vancomycin in normal saline bags due to a lack of sterility assurance. The products were distributed in six states.

    Product
    Vancomycin various strengths in normal saline bags
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0361-2015·2015-01-28

    Acyclovir Infusion Recall Due to Lack of Sterility Assurance

    Walgreens Infusion Services is recalling Acyclovir in normal saline due to lack of sterility assurance. The products were distributed in six states.

    Product
    Acyclovir various strengths in normal saline
    Category
    Drug
    Distribution
    6 states
  • SevereNHTSA·15V043000·2015-01-28

    Toyota Recalls 2003-2004 Corolla, Avalon, and Pontiac Vibe for Air Bag Defect

    Toyota is recalling 2003-2004 Corolla, Corolla Matrix, Avalon, and Pontiac Vibe vehicles because electrical noise may cause air bags to deploy unexpectedly.

    Product
    TOYOTA — TOYOTA, PONTIAC COROLLA MATRIX, COROLLA, AVALON, VIBE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0353-2015·2015-01-28

    Walgreens Recalls Cefazolin Infusion Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling Cefazolin in normal saline bags due to a lack of sterility assurance. The products were distributed in six southern states.

    Product
    Cefazolin various strengths in normal saline bags
    Category
    Drug
    Distribution
    6 states
  • SevereNHTSA·15V046000·2015-01-28

    Chrysler Recalls Jeep and Dodge Vehicles for Air Bag Defect

    Chrysler is recalling specific 2002-2004 Jeep and Dodge vehicles because electrical noise may cause air bags to deploy unexpectedly, increasing injury risk.

    Product
    JEEP — JEEP, DODGE LIBERTY, GRAND CHEROKEE, VIPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0368-2015·2015-01-28

    Walgreens Recalls Ranitidine Syringes Due to Sterility Assurance Concerns

    Walgreens Infusion Services is recalling various strengths of ranitidine syringes because of a lack of sterility assurance. The products were distributed in six states.

    Product
    Ranitidine various strengths in syringes
    Category
    Drug
    Distribution
    6 states
  • SevereNHTSA·15V044000·2015-01-28

    GM Recalls 2015 SUVs for Tread Cracking Tire Defect

    General Motors is recalling 2015 Buick Enclave, Chevrolet Traverse, and GMC Acadia vehicles equipped with specific Goodyear tires that may experience tread cracking, increasing crash risk.

    Product
    GMC — GMC, CHEVROLET, BUICK ACADIA, TRAVERSE, ENCLAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·022-2015·2015-01-28

    Washington Beef Recalls Boneless Beef Trim Due To E. Coli O157:H7 Risk

    Washington Beef, LLC is recalling 1,620 pounds of boneless beef trim product that may be contaminated with E. coli O157:H7. The product was distributed to a grinding facility in Oregon and Washington.

    Product
    Washington Beef, LLC — Washington Firm Recalls Boneless Beef Trim Product Due To Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0375-2015·2015-01-28

    Walgreens Infusion Services Recalls Total Parenteral Nutrition Products

    Walgreens Infusion Services is recalling total parenteral nutrition products due to a lack of sterility assurance. The products were distributed in six states.

    Product
    Total parenteral nutrition various strengths
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0356-2015·2015-01-28

    Walgreens Recalls Daptomycin Infusion Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling Daptomycin in normal saline bags due to a lack of sterility assurance. The products were distributed in six southern states.

    Product
    Daptomycin various strengths in normal saline bags
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0348-2015·2015-01-28

    Walgreens Recalls Piperacillin/Tazobactam Infusion Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling piperacillin/tazobactam in normal saline bags due to a lack of sterility assurance. The products were distributed in six southern states.

    Product
    Piperacillin/ tazobactam various strength in normal saline bags
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0344-2015·2015-01-28

    Walgreens Recalls Cefoxitin Infusion Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling Cefoxitin in normal saline bags due to a lack of sterility assurance. The products were distributed in six states.

    Product
    Cefoxitin various strength in normal saline bags
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0374-2015·2015-01-28

    Walgreens Recalls L-cysteine Infusions Due to Sterility Concerns

    Walgreens Infusion Services is recalling L-cysteine products due to a lack of sterility assurance. The affected products were distributed in six southern states.

    Product
    L-cysteine various strengths
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0366-2015·2015-01-28

    Walgreens Recalls Folic Acid Syringes Due to Sterility Concerns

    Walgreens Infusion Services is recalling folic acid pre-drawn syringes due to a lack of sterility assurance. The products were distributed in six states.

    Product
    Folic acid 1 mg/ 0.2 ml pre-drawn syringes
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0342-2015·2015-01-28

    Walgreens Recalls Aztreonam Infusions Due to Sterility Concerns

    Walgreens Infusion Services is recalling Aztreonam 1 gram in normal saline due to a lack of sterility assurance. The affected products were distributed in six states.

    Product
    Aztreonam 1 gram in normal saline
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Devices)·Z-0996-2015·2015-01-28

    TransMotion Medical Recalls Powered Stretcher Chairs Due to Involuntary Movement

    TransMotion Medical Inc is recalling 1,127 powered stretcher chairs used in surgeries because the controllers may cause the chairs to move involuntarily.

    Product
    Powered stretcher chair used during facial and eye surgeries. One chair per package.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0379-2015·2015-01-28

    Valeant Recalls Virazole Due to Microbial Contamination

    Valeant Pharmaceuticals is recalling Virazole (ribavirin) inhalation solution due to positive microbial contamination found during stability testing.

    Product
    Virazole (Ribavirin for Inhalation Solution, USP), Sterile Lyophilized For Administration by Aerosol Inhalation Only, Rx only, Contents: Four 6 g vials, 100 mL, Distributed by: Valeant Pharmaceuticals North America, Bridgewater, NJ 08807 USA, NDC 0187-0007-14.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0358-2015·2015-01-28

    Walgreens Recalls Levofloxacin Infusions Due to Sterility Concerns

    Walgreens Infusion Services is recalling levofloxacin infusions in normal saline due to a lack of sterility assurance. The products were distributed in six southern states.

    Product
    Levofloxacin various strengths in normal saline
    Category
    Drug
    Distribution
    6 states
  • SevereNHTSA·15V042000·2015-01-28

    Land Rover Recalls Range Rover Models for Brake Vacuum Hose Routing Issue

    Jaguar Land Rover is recalling 2013-2015 Range Rover and Range Rover Sport vehicles because a brake vacuum hose may be incorrectly routed, potentially causing a loss of braking assistance.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT, RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0355-2015·2015-01-28

    Walgreens Recalls Gentamicin Infusion Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling Gentamicin in normal saline bags due to a lack of sterility assurance. The products were distributed in six states.

    Product
    Gentamicin various strength in normal saline bags
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0377-2015·2015-01-28

    Mylan Recalls Ciprofloxacin Tablets Due to Manufacturing Deviations

    Mylan Institutional, Inc. is recalling Ciprofloxacin Tablets 500 mg because they were produced with active ingredients not manufactured according to Good Manufacturing Practices.

    Product
    CIPROFLOXACIN TABLETS, USP, 500 mg, 100 Tablets (10 tablets per blister card. 10 blister cards per carton), Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 51079-182-20.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0341-2015·2015-01-28

    Walgreens Recalls Amikacin Infusion Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling Amikacin in normal saline bags due to a lack of sterility assurance. The products were distributed in six states.

    Product
    Amikacin various strength in normal saline bags
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0350-2015·2015-01-28

    Walgreens Recalls Cefuroxime Infusion Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling cefuroxime in normal saline bags due to a lack of sterility assurance. The products were distributed in six southern states.

    Product
    Cefuroxime various strengths in normal saline bags
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0345-2015·2015-01-28

    Walgreens Recalls Ceftazidime Infusion Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling Ceftazidime in normal saline bags due to a lack of sterility assurance. The products were distributed in six states.

    Product
    Ceftazidime various strength in normal saline bags
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0351-2015·2015-01-28

    Walgreens Recalls Meropenem Infusion Bags Due to Sterility Concerns

    Walgreens Infusion Services is recalling Meropenem in normal saline bags due to a lack of sterility assurance. The products were distributed in six states.

    Product
    Meropenem various strengths in normal saline bags
    Category
    Drug
    Distribution
    6 states
  • HighFDA (Food)·F-0923-2015·2015-01-28

    Roland Bruschetta Recalled Due to Glass Fragment Contamination

    American Roland Food Corp. is recalling Roland brand Bruschetta, Italian-Style Appetizer, because glass fragments were found in the product.

    Product
    Roland brand Bruschetta, Italian-Style Appetizer, NET WT. 12 OZ. (340g), Item 46740, UPC 41224467408, PRODUCT OF TURKEY ---The product is packaged in a glass jar, 12 x 12 oz. jars per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0995-2015·2015-01-28

    Ferno Model 35X Stretchers Recalled Due to Loose Wheel Assemblies

    Ferno-Washington Inc is recalling 46 Model 35X stretchers because wheel castor assemblies may loosen, posing a risk of injury.

    Product
    Ferno Model 35X PROFlexx Stretchers, one unit per package
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0994-2015·2015-01-28

    Siemens Radiographic Systems Recalled for Potential Image Flipping Errors

    Siemens is recalling 11 Ysio Max, Luminos dRF Max, and Agile Max systems because software errors may cause images to flip, leading to incorrect labels and potential misdiagnosis.

    Product
    Ysio Max, Luminos dRF Max and Agile Max systems with software version VE10 and SmartOrtho license. The Ysio Max is a radiographic system used in hospitals, clinics, and medical practices. Ysio Max enables radiographic and tomographic exposures of the whole body including: skul
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Food)·F-0799-2015·2015-01-28

    QuestBar Protein Bars Recalled for Possible Plastic Contamination

    Quest Nutrition is recalling specific lots of QuestBar protein bars due to the possibility of plastic pieces introduced by an ingredients supplier.

    Product
    QuestBar Protein Bar Double Chocolate Chunk Flavor NET Wt. 2.12 OZ (60g) Lot #: 1BA4DCC14289 Exp Date: October 17, 2015 UPC Codes: - individual bar: 7-93573-22592-4 - caddie: 7-93573-22591-7 The protein bar is wrapped in a plastic wrapper containing labeling informati
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0796-2015·2015-01-28

    Giant Eagle Recalls Jumbo Lump Crab Cakes Due to Undeclared Milk

    Giant Eagle is recalling Jumbo Lump Crab Cakes in Pennsylvania and Ohio because the ingredient statement failed to declare milk.

    Product
    Jumbo Lump Crab Cakes packed from bulk into clam shell containers with Giant Eagle scale label 100% Jumbo Lump Crab Cake Sell by Date: any date Net Wt. any weight Giant Eagle Market District Distributed by Giant Eagle, Pittsburg, PA 15328
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·15V045000·2015-01-28

    Honda Recalls 2003-2004 Odyssey and 2003 Acura MDX for Air Bag Defect

    Honda is recalling 2003-2004 Odyssey and 2003 Acura MDX vehicles because electrical noise may cause air bags to deploy unexpectedly, increasing injury risk.

    Product
    HONDA — HONDA, ACURA ODYSSEY, MDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1003-2015·2015-01-28

    Dick's Sporting Goods Recalls Fitness Gear Inversion Tables Due to Injury Reports

    Dick's Sporting Goods is recalling Fitness Gear Inversion Tables because customers reported falling and sustaining injuries. The products were distributed nationwide.

    Product
    Fitness Gear Inversion table (Style STE00059FG or Style STE00118FG), Distributed by ASLI, Wilmington, DE (on carton), Paradigm Health & Wellness, Inc. (in user manuals); The products are inversion tables, which allow the user to secure his or her ankles to the table and invert.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1000-2015·2015-01-28

    BD Biosciences Recalls Contaminated CD8 PE In Vitro Diagnostic Reagent

    BD Biosciences is recalling one lot of CD8 PE reagent contaminated with CD4 FITC, which may cause incorrect patient data.

    Product
    CD8 (Leu-2a) PE (In vitro diagnostic), Catalog number 340046. Hematology: Single color direct immunofluorescence reagent for enumerating percentages of mature human suppressor/cytotoxic (CD8+) lymphocytes in erythrocyte-lysed whole blood or peripheral blood mononuclear cell su
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0993-2015·2015-01-28

    Maquet Tegris System Recalled Due to Software Error in Operating Table Commands

    Maquet Medical Systems USA is recalling six units of the Tegris System because a software error switches leg movement commands for the Magnus OR table.

    Product
    TEGRIS System manufactured by MAQUET GMBH in Germany The Maquet Tegris OR Integration System is designed to be used as the central operating unit in an operating room. The integration system has two main functions: Recording and distribution of images and videos and interaction
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0998-2015·2015-01-28

    Cordis POWERFLEX PRO PTA Dilatation Catheter Recall for Unsterilized Unit

    Cordis Corporation is recalling one unsterilized unit of the POWERFLEX PRO PTA Dilatation Catheter from a demonstration lot left at a hospital.

    Product
    Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal, infra popliteal and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. The device is also indic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V040000·2015-01-28

    Ford Recalls Taurus and Lincoln MKS for Door Handle Spring Defect

    Ford is recalling 2010-2013 Taurus and 2011-2013 Lincoln MKS vehicles because an interior door handle spring may unseat, preventing the handle from returning to its stowed position.

    Product
    LINCOLN — LINCOLN, FORD MKS, TAURUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0800-2015·2015-01-28

    Quest Nutrition Recalls Protein Bars Due to Possible Plastic Contamination

    Quest Nutrition is recalling specific lots of QuestBar protein bars because they may contain plastic pieces from an ingredient supplier.

    Product
    QuestBar Protein Bar Chocolate Chip Cookie Dough Flavor NET Wt. 2.12 OZ (60g) Lot #: 1BA6CCD14294 UPC Codes: - individual bar: 7-93573-21453-9 - caddie: 7-93573-21454-6 Production date: 10/22/14 Exp Date: 10/21/15 The protein bar is wrapped in a plastic wrapper cont
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-0798-2015·2015-01-28

    Baroody Pickled Labneh Recalled for Undeclared Sorbic Acid

    Baroody Imports Inc. is recalling 9 cases of Baroody Pickled Labneh with Garlic in New York due to undeclared sorbic acid.

    Product
    Baroody Pickled Labneh with Garlic, Net Wt. 20 oz., (1 lb. 4 oz.), 575-g, in sealed glass jar, UPC 642036011164
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1002-2015·2015-01-28

    BD Biosciences Recalls Contaminated Anti-Lambda APC-H7 Antibody Lots

    BD Biosciences is recalling two lots of Anti-Lambda APC-H7 antibody due to contamination with CD38 antibody. The product is used for in vitro flow cytometric immunophenotyping.

    Product
    Anti-Lambda APC-H7, Catalog Number 656157. Product Usage: Intended for in vitro flow cytometric immunophenotyping of hematologic disorders.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1001-2015·2015-01-28

    Genetic Testing Institute Recalls PF4 Concentrated Wash Reagent Lots

    Genetic Testing Institute is recalling specific lots of PF4 Concentrated Wash (10x) because the reagent is slightly more dilute than intended, which may cause false positive test results.

    Product
    PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG (catalog numbers HAT13G, HAT45G) and 2. ImmucorGamma LIFECODES PF4 Enhanced (catalog numbers X-HAT13, X-HAT45) The PF4 IgG assay is an Enzyme Linked Immunosorb
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0997-2015·2015-01-28

    Philips IntelliVue TcG10 Monitor Recalled for Missing Contraindication Warning

    Philips is recalling 86 IntelliVue TcG10 monitors because the instructions for use are missing a warning against using the device on patients under gas anesthesia.

    Product
    Philips IntelliVue TcG10; Monitor, carbon-dioxide, cutaneous. The IntelliVue TcG10 is a device for the measurement of the transcutaneous O2 and CO2 partial pressure in neonates, pediatrics and adults.
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Food)·F-0797-2015·2015-01-28

    Baroody Pickled Labneh Recalled for Undeclared Sorbic Acid and Sulfites

    Baroody Imports Inc. is recalling Baroody Pickled Labneh with Pepper because the product contains undeclared sorbic acid and sulfites.

    Product
    Baroody Pickled Labneh with Pepper, Net Wt. 20 oz., (1 lb. 4 oz.), 575-g, in sealed glass jar, UPC 642036010549
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0378-2015·2015-01-28

    Mylan Lamotrigine Tablets Recalled for CGMP Deviations

    Mylan Institutional is recalling 3,993 cartons of Lamotrigine 200 mg tablets because they were not manufactured according to Good Manufacturing Practices.

    Product
    LAMOTRIGINE TABLETS, 200 mg, 100 Tablets (10 tablets per blister card x 10 blister cards per carton), Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 51079-866-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0370-2015·2015-01-28

    Walgreens Recalls Deferoxamine Infusions Due to Sterility Concerns

    Walgreens Infusion Services is recalling Deferoxamine in normal saline due to a lack of sterility assurance. The products were distributed in six states.

    Product
    Deferoxamine various strengths in normal saline
    Category
    Drug
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0999-2015·2015-01-28

    Roche Recalls cobas 4800 KRAS Mutation Test Kits for Invalid Results

    Roche Molecular Systems is recalling cobas 4800 KRAS Mutation Test kits because they are generating invalid results for the Mutant Control and/or KRAS Calibrator.

    Product
    cobas 4800 KRAS AMP/DET 24T CE-IVD Mutation Test; CE-IVD 5852170190. Intended for the identification of mutations in codons 12,13 and 61 of the KRAS Gene in DNA derived from formalin-fixed paraffin-embedded human colorectal and non-small cell lung cancer tissues.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1007-2015·2015-01-28

    Arrow Hemodialysis Catheterization Sets Recalled for Tunneling Sheath Cracking

    Arrow International is recalling specific hemodialysis catheterization sets because the tunneling sheath can crack during placement, potentially delaying treatment.

    Product
    The Arrow Edge Hemodialysis Catheterization Set Long-Term Access and NextStep Antegrade Hemodialysis Catheterization Set, Long-Term Access, part numbers: AC-15192-SFX, AC-15232-SFX, AC-15272-SFX, AC-15312-SFX, AC-15422-SFX, CS-15192-SFX, CS-15192-SFXM, CS-15232-SFX, CS-15242-I, C
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-1004-2015·2015-01-28

    Ortho-Clinical VITROS Software Recall Due to Calibration Failure

    Ortho-Clinical Diagnostics is recalling VITROS Software Version 3.1 because calibration may not occur when using specific calibrator barcode labels.

    Product
    VITROS Software Version 3.1 utilized on the following systems: 1) 4600 Chemistry Systems (VITROS 5,1 FS System family member, 2) 5600 Integrated System 1) VITROS 4600 - in vitro quantitative measurement of a variety of analytes, 2) VITROS 5600 - in vitro quantitative, semi-qua
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Drugs)·D-0376-2015·2015-01-28

    3M ESPE Clinpro 5000 Toothpaste Recalled for Missing Lot and Expiration Dates

    3M ESPE is recalling 19,728 tubes of Clinpro 5000 Anti-Cavity Toothpaste because the primary boxes are missing lot numbers and expiration dates.

    Product
    3M ESPE Clinpro 5000 (1.1% Sodium Flouride), Anti-Cavity Toothpaste, 4 oz tube (NDC 48878-3130-04), Rx Only, Manufactured for 3M ESPE Dental Products, St. Paul, MN 55144
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1005-2015·2015-01-28

    Arrow International Recalls Multi-Lumen CVC Kits Due to Missing Instructions

    Arrow International Inc is recalling 420 Multi-Lumen PI CVC Kits and PSI Kits because the Instructions for Use were inadvertently removed from the packaging.

    Product
    Multi-Lumen PI CVC Kit and PSI Kit: 3-L 7 FR X 8 product code: ASK-45703-POSU lot #23F13L0166, exp. 31-Jul-2015: Product Usage: Multi-Lumen PI CVC Kit: An intravascular catheter is a device that consists of a slender tube and any necessary connecting fittings and that is i
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-1006-2015·2015-01-28

    Aptalis Flutter Percussor Respiratory Device Recalled for Packaging Defect

    Aptalis Pharmatech Inc. is recalling approximately 49,000 Flutter Percussor respiratory devices because the packaging may be difficult to open or close.

    Product
    FLUTTER Percussor respiratory device, packaged one unit per clear plastic package. Product Usage: Product is a percussor device, intended to be used as a mucus clearance device for patients with mucus producing respiratory conditions such as: atelectasis, bronchitis, bronch
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V039000·2015-01-27

    Land Rover Recalls Range Rovers Due to Brake Hose Rupture Risk

    Jaguar Land Rover is recalling 2006-2012 Range Rovers because front brake hoses may rupture, causing loss of brake fluid and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V035000·2015-01-27

    Crossroads Recalls 2015 Z1 Trailers Due to Incorrect Ramp Load Labels

    Crossroads RV is recalling 2015 Z1 toyhauler trailers because the front loading ramps display a 700-pound capacity limit, but the actual limit is 500 pounds.

    Product
    CROSSROADS — CROSSROADS Z1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15064·2015-01-27

    Mirka Recalls Compact Electric Random Orbital Sanders Due to Fire Hazard

    Mirka Abrasives is recalling specific 5-inch and 6-inch compact electric random orbital sanders because they can short circuit, posing a fire hazard. No injuries or property damage have been reported.

    Product
    Random orbital sanders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V036000·2015-01-27

    Peterbilt 389 Recall for Electronic Stability Control Sensor Defect

    PACCAR is recalling 2015 Peterbilt 389 trucks because an incorrect horn contact plate may damage the ESC steering angle sensor, increasing crash risk.

    Product
    PETERBILT — PETERBILT 389
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V037000·2015-01-27

    Jaguar Recalls 2015 XJ Models for Incorrect Air Bag Manual Description

    Jaguar is recalling 1,346 model year 2015 XJ vehicles because the owner's manual incorrectly describes the Occupant Sensor System, potentially increasing injury risk in a crash.

    Product
    JAGUAR — JAGUAR XJ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V038000·2015-01-27

    Jaguar Recalls 2012-2015 XK Models for Front Side Lamp Defect

    Jaguar is recalling 2012-2015 XK vehicles because front side lamps may turn off after five minutes, reducing visibility and increasing crash risk.

    Product
    JAGUAR — JAGUAR XK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·021-2015·2015-01-26

    Oscar's Hickory House Recalls Sausage for Undeclared Allergens

    Oscar's Hickory House is recalling approximately 376 pounds of sausage products due to misbranding and undeclared allergens, including soy, milk, wheat, and sulfites.

    Product
    Oscar's Hickory House Inc. — New York Firm Recalls Sausage Products Due to Misbranding and An Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V033000·2015-01-26

    Nissan and Infiniti Recall Vehicles Due to Hood Latch Defect

    Nissan is recalling specific 2013-2014 Pathfinder, JX35, and QX60 models because the hood latch may not engage fully, posing a crash risk if the hood opens while driving.

    Product
    INFINITI — INFINITI, NISSAN QX60 HYBRID, PATHFINDER HYBRID, PATHFINDER, JX35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V031000·2015-01-26

    GM Recalls 2015 Chevrolet Corvettes for Rear Suspension Defect

    General Motors is recalling 2015 Chevrolet Corvettes because a rear suspension part may not be tightened properly, which could separate and cause a crash.

    Product
    CHEVROLET — CHEVROLET CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V032000·2015-01-26

    Nissan Recalls Rogue Vehicles Due to Electrical Fire Risk

    Nissan is recalling 2008-2014 Rogue vehicles because an electrical short in the driver-side floor can cause a vehicle fire. Dealers will inspect and repair the wiring harness free of charge.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E004000·2015-01-26

    Cummins Recalls QSK50 Dual Fuel Engines Due to Fuel Leak Risk

    Cummins is recalling QSK50 Tier 2 Dual Fuel Engines used on oil well fracturing rigs because a cracked fuel inlet connection may cause a leak and increase fire risk.

    Product
    FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowNHTSA·15V034000·2015-01-26

    MINI Cooper Recalled for Incorrect Tire Information Placard Weight Label

    BMW is recalling 2014-2015 MINI Cooper Hardtop vehicles because the Tire Information Placard lists an incorrect maximum capacity weight, failing to comply with federal safety standards.

    Product
    MINI — MINI COOPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·020-2015·2015-01-23

    Primecut Meats Recalls Chicken Breast Fritters for Undeclared Egg Allergen

    Primecut Meats is recalling approximately 17,700 pounds of chicken breast fritters because the products contain eggs, a known allergen, that are not declared on the label.

    Product
    Arizona Firm Recalls Chicken Breast Fritters Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·15T002000·2015-01-23

    Goodyear Recalls Fortera HL Tires Due to Tread Cracking

    Goodyear is recalling specific Fortera HL tires due to tread cracking that could cause tire failure. Owners of affected 2015 GM vehicles or replacement tires should contact the manufacturer.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V027000·2015-01-23

    Autocar Recalls 2015 Xpeditor Trucks for Fuel Filter Defect

    Autocar is recalling 38 model year 2015 Xpeditor trucks because a fuel filter defect may cause the engine to stall without warning, increasing the risk of a crash.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V028000·2015-01-23

    Volkswagen Recalls 2014-2015 Models for Fuel Rail Leak Risk

    Volkswagen is recalling specific 2014-2015 Jetta, Passat, Golf, GTI, and Beetle models because a fuel rail sealing cap may fail, allowing fuel to leak into the engine compartment.

    Product
    VOLKSWAGEN — VOLKSWAGEN BEETLE, JETTA, GTI, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·019-2015·2015-01-23

    Aspen Foods Recalls Chicken Steaks Due to Undeclared Allergens

    Aspen Foods is recalling approximately 1,140 pounds of chicken steak products because they contain undeclared wheat and soy allergens.

    Product
    Illinois Firm Recalls Chicken Steak Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·15E003000·2015-01-23

    Nova Bus Recalls N67588 Alternator Cables for Fire Risk

    Nova Bus is recalling N67588 alternator cables for 2010-2014 LFS transit buses because damaged terminals may arc and cause an engine compartment fire.

    Product
    ELECTRICAL SYSTEM:ALTERNATOR/GENERATOR/REGULATOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide

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