Archive
675 recalls were announced in September 2014.
Of the 675 recalls this month scored against our rubric, 9% are Critical, 22% are Severe.
Which agencies issued them
Eldorado is recalling 2006-2014 coaches equipped with certain Ricon wheelchair lifts because the platform side plate may crack, posing an injury risk.
Tiffin is recalling 2013-2015 Allegro Bus motorhomes because the Federal Certification label incorrectly states the front Gross Axle Weight Rating.
Chantique's Corp. is recalling Pure Baby Organics boy's hoodies because the neck drawstrings pose a strangulation risk to children.
Trimfoot is recalling First Impressions high-top soft-soled sneakers for infants because metal eyelets can detach and pose a choking hazard. No injuries have been reported.
Franklin Fueling Systems is recalling about 6,700 Hardwall Fuel Curb Hoses because a loose crimp can cause fuel leaks, posing a fire and explosion hazard.
Eldorado is recalling 2006-2007 MST and Transmark buses because wheelchair lift platform side plates may crack, posing an injury risk to operators.
Active Apparel is recalling boys' Fission zipper hooded sweatshirts because neck drawstrings pose a strangulation hazard. No injuries have been reported.
Husqvarna is recalling about 700 Craftsman push mowers sold at Orchard Supply Hardware because the engine control lever can fail, posing an injury risk.
Campagna is recalling certain T-Rex 14 motorcycles because the engine oil pan may hit the road, causing an oil leak and loss of traction.
Diamond Coach is recalling 45 model year 2006-2011 PT and VIP buses because wheelchair lift platform side plates may crack, posing an injury risk.
Sam Kane Beef Processors is recalling approximately 2,633 pounds of ground beef chubs that may contain small pieces of blue plastic.
Navistar is recalling 78 model year 2015 International TranStar vehicles because a clutch rod nut may be missing or loose, which could cause the vehicle to lunge unexpectedly and increase crash risk.
Toyota is recalling 2005-2011 Tacoma Pre-Runner and 4x4 vehicles because a rear leaf spring may fracture and puncture the fuel tank, increasing fire risk.
Emerson is recalling specific Fisher pressure relief valves used in cargo tank trailers because they may break and eject, posing risks of injury, fire, or road hazards.
Mitsubishi Fuso is recalling 2012-2015 FEC52, FEC72, FEC92, and FGB72 trucks because the automatic transmission fluid oil cooler hose may burst, potentially causing the transmission to fail and increasing crash risk.
Newmar is recalling 2007-2012 motorhomes because an incorrectly rated circuit breaker for the refrigerator water line may increase fire risk.
Crossroads is recalling 2015 Zinger Z-1 and Cruiser trailers because incorrect weight labels may lead to overloading and tire failure.
Delicious Beef Jerky, LLC is recalling 8 pounds of Lemon Pepper Seasoned Beef Jerky because the products were produced and shipped without the required USDA inspection.
Ford is recalling 2013-2014 C-Max, Fusion, Escape, and Lincoln MKZ vehicles because a defect in the Restraint Control Module may prevent airbags and seat belt pretensioners from functioning in a crash.
Polaris is recalling 2015 Victory motorcycles because a transmission spring may be installed incorrectly, potentially causing loss of control.
Mercedes-Benz is recalling 2015 C300 and C400 vehicles because a steering component may disengage, potentially causing loss of control.
Forest River is recalling 2006-2014 Glaval buses equipped with certain Ricon wheelchair lifts because the platform side plate may crack, posing a risk of injury.
Altec is recalling 2011-2014 DC1317 wood chippers because fasteners may fail, causing the cutting disc to detach and injure operators.
Collins is recalling 2006-2014 school buses equipped with specific Ricon wheelchair lifts because the platform side plate may crack, posing an injury risk.
Foster Farms is recalling approximately 39,747 pounds of frozen chicken breast strips due to possible Listeria monocytogenes contamination. The product was distributed to California, Texas, Utah, and Washington.
Caviness Beef Packers is recalling approximately 23,100 pounds of beef trimmings produced in August 2014 due to possible E. coli O157:H7 contamination.
Ross Stores is recalling about 840 metal bistro chairs because the seat can fail to attach to the frame, posing a fall hazard.
Bad Boy Buggies is recalling about 4,460 recreational off-road vehicles because brake issues can reduce braking ability, posing a crash hazard.
Shivvers is recalling about 1,650 Country Clipper riding lawn mowers in the U.S. and 261 in Canada because the ignition module can overheat and melt, posing a fire hazard.
Nova Products, Inc. is voluntarily recalling Mojo Risen because FDA testing found undeclared sildenafil, an active ingredient in erectile dysfunction drugs.
Vibrant Health is recalling Rainbow Vibrance Hi ORAC Superfood because a raw material used in its manufacture was found to contain Salmonella bacteria.
Nova Products, Inc. is voluntarily recalling Xzen 1200 capsules because FDA analysis found undeclared sildenafil and tadalafil, active ingredients in erectile dysfunction drugs.
Baxter Healthcare is recalling 390,560 bags of 0.9% Sodium Chloride Injection USP due to the presence of particulate matter, including fibers and plastics.
American Health Packaging is recalling 137,300 Ibuprofen 600 mg tablets because some cartons were mis-labeled as Oxcarbazepine 300 mg.
Nova Products, Inc. is voluntarily recalling African Black Ant capsules because FDA testing found undeclared sildenafil, an active ingredient in erectile dysfunction drugs.
Nova Products, Inc. is voluntarily recalling Black Ant capsules because FDA analysis found undeclared sildenafil, an active ingredient in erectile dysfunction drugs.
Swanson Health Products is recalling 544 containers of 1 lb Certified Organic Carob Powder due to a potential risk of Salmonella contamination from a raw ingredient.
Vibrant Health is recalling Green Vibrance 15 dietary supplements because a raw material used in manufacturing was found to contain Salmonella bacteria.
Nature's Universe is recalling ThinoGenics dietary supplements because they contain undeclared sibutramine and were marketed without FDA approval.
Bristol-Myers Squibb is recalling Coumadin for Injection vials because metallic-like and cellulose fiber particles were found in retained samples.
Nova Products, Inc. is voluntarily recalling XZEN GOLD capsules because FDA testing found undeclared sildenafil and tadalafil.
Nova Products, Inc. is voluntarily recalling XZEN Platinum capsules because FDA analysis found undeclared sildenafil and tadalafil.
Dean Foods is recalling Swiss Premium 100% Pure Orange Juice from Concentrate in half-gallon and one-gallon plastic containers due to undeclared dairy ingredients.
Brooks Tropicals, LLC is recalling avocados found positive for Salmonella. The affected product was distributed in Florida, Georgia, Illinois, New Jersey, and New York.
Dean Foods is recalling Lehigh Valley Dairy Farms Orange Juice from Concentrate because it contains undeclared dairy. The product was distributed in several Mid-Atlantic states and Washington, DC.
Baxter Healthcare is recalling specific lots of 0.9% Sodium Chloride Injection USP bags due to the presence of particulate matter, including fibers and plastics.
Dean Foods is recalling Lehigh Valley Dairy Farms Orange Juice from concentrate because it contains undeclared dairy. The product was distributed in several Mid-Atlantic states.
Daimler Trucks North America is recalling 2014-2015 FCCC truck chassis because improperly secured propane fuel injectors or leaking tubes may cause a stall or fire.
EMG Technology is recalling 1,452 Vac-Assist Suction Units because the canister lids may have occluded ports, potentially preventing proper fluid removal.
General Motors is recalling 2013-2015 Chevrolet Sparks because the secondary hood latch may corrode, potentially allowing the hood to open while driving.
International Sprout Holding Inc. is recalling Crimson Clover seed because it tested positive for Listeria Monocytogenes. The product was distributed in six states and Puerto Rico.
American Health Packaging is recalling Oxcarbazepine Tablets due to a label mix-up with Ibuprofen tablets.
Nova Products, Inc. is voluntarily recalling XZone 1200 capsules because FDA analysis found undeclared sildenafil and tadalafil.
Vibrant Health is recalling Green Vibrance dietary supplements because a raw material used in manufacturing was found to contain Salmonella bacteria.
Dole Fresh Vegetables is recalling 6 oz bags of Baby Spinach because green walnuts were found on the processing line. The product was distributed in Arizona, New Mexico, and Nevada.
Nova Products, Inc. is voluntarily recalling XZONE GOLD capsules because FDA testing found undeclared sildenafil and tadalafil.
Specialty Commodities, Inc. is recalling Thien Minh Cashew Kernels due to potential Salmonella contamination. The product was distributed in Colorado and New Jersey.
Unique Pharmaceutical is recalling 430 bags of Repinephrine 4 mg in 250 mL Sodium Chloride 0.9% because a mold-like substance was found on an unopened bag during production.
Polar Tank is recalling 2014 SRJ7 trailers because suspension pivot bolts may fail, causing the axle to separate and increasing crash risk.
Vibrant Health is recalling Green Vibrance dietary supplement powder because a raw material used in its manufacture was found to contain Salmonella bacteria.
Baxter Healthcare is recalling 171,672 bags of Potassium Chloride Injection due to the presence of particulate matter, including fibers and plastics.
Dean Foods is recalling 140 gallons of Price Chopper Orange Juice because it contains undeclared dairy, a major allergen.
Calavo Growers is recalling specific avocados because they may be contaminated with Salmonella. The affected product was distributed in Washington, Illinois, and Wisconsin.
Elkhart Coach is recalling 2006-2014 Ford E-350 and E-450 vans equipped with specific Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk.
JK Products & Services is recalling 1,948 Sun Dash Radius 252 tanning beds because excessive flexing of the main electrical cord can compromise wire integrity.
Varian Medical Systems is recalling 512 4D Integrated Treatment Consoles because user error can allow improper clearing of safety interlocks.
Volcano Corporation is recalling TrakBack II Disposable Pullback Devices because internal testing identified a potential breach to the sterile barrier that may impact product sterility.
Data Innovations, LLC is recalling ProVue Instrument Driver for JResultNet versions 1.5.3 and below because the software may misassociate data with patient results.
Varian Medical Systems is recalling C-Series High Energy Linear Accelerators due to a trend of unexpected decreases in beam output during 6MV photon treatment.
Hospira Inc. is recalling 75,000 vials of Bupivacaine Hydrochloride 0.5% due to a confirmed report of a brown, rust-colored particle embedded in the glass vial.
Bio-Detek is recalling 198 cases of ZOLL Pro-padz Sterile Adult Multi-Function Electrodes because the sterility of the devices is not assured.
Mitsubishi Heavy Industries is recalling three Vero Linear Accelerator systems in the US due to a software defect that may incorrectly mark completed radiation treatments as untreated.
Mt. Sterling Coop Creamery is recalling specific lots of raw goat milk cheddar cheese due to potential contamination with Shiga toxin-producing E. coli O111:H8.
Bio-Detek, Inc. is recalling ZOLL Pro-padz Sterile Adult Multi-Function Electrodes because the sterility of the devices is not assured.
Motion Concepts is recalling 59 TRx Vertical Positioner units because knee supports may fail due to bolt fatigue.
Becton Dickinson is recalling specific lots of Vancomycin Screen Agar because the product may allow susceptible bacteria to grow, leading to false resistance test results.
ArjoHuntleigh is recalling Tenor mobile passive lifts because the spreader bar bolt may break during use, posing a risk to patients and caregivers.
Bio-Detek is recalling ZOLL Pro-padz Sterile Adult Multi-Function Electrodes because the sterility of the devices is not assured.
Siemens is recalling ADVIA Chemistry A1c_3 Calibrators because they may cause a percent bias in HbA1c test results.
Nestle USA is recalling Lean Cuisine Chicken with Peanut Sauce due to package mislabeling regarding peanut content.
Jenis Splendid Ice Creams LLC is recalling Forest Berry Sorbet because the frozen dessert packaging does not list ingredients, posing a risk to consumers with allergies.
Jenis Splendid Ice Creams LLC is recalling Cranberry Royale frozen dessert because the packaging does not list ingredients, posing a risk to consumers with food allergies.
Japanese Specialty Food Distributors is recalling 961 cases of frozen ground tuna from Indonesia due to an association with scombroid illness. The product was distributed to Connecticut, New York, New Jersey, Texas, and Georgia.
Dole Fresh Vegetables is recalling 8 oz bags of spinach because green walnuts were found on the processing line.
Jenis Splendid Ice Creams LLC is recalling Cocoa Zin frozen dessert because the packaging does not list ingredients, posing a risk to consumers with allergies.
Genesis BPS, LLC is recalling 4,608 units of Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringes because the company failed to notify the FDA of material changes.
Jenis Splendid Ice Creams LLC is recalling Sweet Corn with Blackberry frozen desserts because the packaging does not list ingredients.
Jenis Splendid Ice Creams LLC is recalling Spiced Pecan Praline frozen desserts because the packaging does not list ingredients.
Genesis BPS, LLC. is recalling 7,272 units of Pedi-Pak Pedi-Syringe Filter 60 mL syringes because the company failed to notify the FDA of material changes.
Jenis Splendid Ice Creams LLC is recalling Backyard Mint Straciatella frozen dessert because the product labeling does not include ingredients.
Fresenius Medical Care is recalling BD Vacutainer PST Tubes because they were held at improper storage temperatures. The affected units were distributed in Louisiana, Oklahoma, and Texas.
Philips is recalling Brilliance 64 and Ingenuity CT systems because CIRS 4.0 Beta 2 software may cause images to overlap during reconstruction.
B. Braun Medical is recalling AccuFlo infusion devices in Missouri due to a mismatch between inner and outer packaging labels.
Bard Peripheral Vascular Inc is recalling Bard DuaLok Breast Lesion Localization Wires because portions of the wire may protrude from the packaging, breaching the sterile barrier.
Jenis Splendid Ice Creams LLC is recalling Pumpkin 5 Spice frozen dessert because the packaging does not list ingredients. The product was distributed to all 50 states.
Jenis Splendid Ice Creams LLC is recalling Lime Cardamom with Lingonberries frozen dessert because the product labeling does not include ingredients.
Teleflex Medical is recalling sterile soft rubber bladder catheters because the product labels failed to include a Natural Rubber Latex caution statement.
Jenis Splendid Ice Creams LLC is recalling Berries and Burgundy frozen desserts because the packaging does not list ingredients.
Beckman Coulter is recalling Coulter DxH Diluent because it may cause elevated platelet background counts, resulting in failed Daily Checks on specific Coulter Cellular Analysis Systems.
Fresenius Medical Care is recalling 9 boxes of BD Vacutainer SST Tubes held at improper storage temperatures. The tubes were distributed in Louisiana, Oklahoma, and Texas.
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