Archive
559 recalls were announced in March 2015.
Of the 559 recalls this month scored against our rubric, 18% are Critical, 26% are Severe.
Which agencies issued them
CPSC recalls Dirt Devil Scorpion Turbo Tool accessories because the internal fan can break and eject, posing a laceration risk to users.
Adams Extract & Spice LLC is recalling specific lots of Multi-Season Seasoned Salt because the product may contain undeclared peanut protein.
Kabobs Inc is recalling frozen Yucatan Style Roasted Corn & Black Bean Tarts because the cumin used contains undeclared peanuts.
Gulf Coast Blenders, Inc. is recalling 10 bags of Dixie Fish Seasoned Flour because the cumin ingredient may contain peanut protein.
Gulf Coast Blenders is recalling Rex King of Spice Cajun Creole Seasoning because the cumin used may contain peanut protein.
J P Veggies Inc. DBA VeggieLand is recalling Chili-Bean Fresh Veggiburgers because they may contain undeclared peanut protein from ground cumin.
Gulf Coast Blenders is recalling REX King of Spice Ground Pati Dry Marinade due to possible peanut protein contamination in the ground cumin ingredient.
Schwan Food Company is recalling Vegetable Samosa Triangles because they may contain undeclared peanut allergen.
Navilyst Medical is recalling 438 NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling 19 units of NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling 16 NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased risk of infection.
Navilyst Medical is recalling 541 NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Zimmer GmbH is recalling 6,109 CoCr femoral heads due to potential sterile tray compromise, which could lead to periprosthetic infection if undetected.
Navilyst Medical is recalling 105 NAMIC Convenience Kits because expiration dating is not fully supported by shelf life testing, which may result in a sterility breach and increased risk of infection.
Navilyst Medical is recalling 562 NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased risk of infection.
Navilyst Medical is recalling NAMIC Convenience Kits because expiration dating is not fully supported by shelf life testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling 411 NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Spacelabs Healthcare is recalling XPREZZON Bedside Monitors because they may fail to boot up or reset to factory defaults after power on.
Philips recalled 238 Multi Diagnost Eleva units because the low-dose mode delivers higher radiation than expected.
Navilyst Medical is recalling 2 units of NAMIC Convenience Kits because expiration dating is not fully supported by shelf life testing, posing a risk of sterility breach and infection.
Navilyst Medical is recalling 180 units of NAMIC Convenience Kits because expiration dating is not fully supported by testing, posing a risk of sterility breach and infection.
Iba Dosimetry GmbH is recalling Compass SW Version 3.1 software for medical linear accelerators due to a dose reconstruction error.
Maquet Datascope is recalling 1,300 CARDIOSAVE Hybrid Intra-Aortic Balloon Pumps due to power supply malfunctions related to suboptimal thermal management.
Navilyst Medical is recalling specific lots of NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling 5 units of NAMIC Convenience Kits because expiration dating is not fully supported by testing, posing a potential sterility breach and infection risk.
KTM North America is recalling about 2,800 children's pajamas and onesies that fail federal flammability standards, posing a risk of burn injuries.
Melville Direct is recalling about 3,600 Aquarium Motion Lamps sold by Bits & Pieces because they can overheat and spark, posing a fire hazard.
Norwex USA Inc. is recalling SilverCare Junior toothbrushes because the head can detach from the handle, posing a choking hazard.
Navilyst Medical is recalling 602 NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased risk of infection.
Navilyst Medical is recalling 74 NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased risk of infection.
Schwan Food Company is recalling 83 cases of Holiday Foods Vegetable Samosa Potstickers due to a potential undeclared peanut allergen.
Navilyst Medical is recalling 30 units of NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased risk of infection.
Zimmer GmbH is recalling 30 Metasul Femoral Head units due to potential sterile tray compromise, which could lead to periprosthetic infection if undetected.
HeartWare Inc is recalling 4,845 HeartWare Controllers used in ventricular assist systems because they are more susceptible to electrostatic discharge (ESD) than newer models.
Navilyst Medical is recalling 2,502 NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling 124 NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Intuitive Surgical is recalling EndoWrist One Vessel Sealers because manufacturing variability may cause interference in the instrument grips.
Angiodynamics is recalling 43 Starburst MRI Semi-Flex Electrode Devices because a printed distance mark is incorrectly located 4cm from the tip instead of 5cm.
Biomet is recalling specific shoulder implant baseplates because a taper adaptor is missing from the packaging, which may delay surgery.
GE Healthcare is recalling 128 Centricity PACS Workstation systems because a software defect may cause exam records to go missing in single Study Mode.
Intuitive Surgical is recalling 3,282 EndoWrist One Vessel Sealers because manufacturing variability may cause interference in the instrument grips.
Sun Pharma Global Fze is recalling specific bottles of Ketorolac Tromethamine Ophthalmic Solution because the product contains particulate matter exceeding specification limits.
Medtronic is recalling specific neurostimulator models because enabling cycling at certain settings may decrease battery life and cause inaccurate longevity estimates on the programmer.
Forest River is recalling 2015 XLR recreational vehicles because incorrect Gross Vehicle Weight Rating (GVWR) labels may lead to hitch overload and loss of control.
Ford is recalling 1,608 Motorcraft steering gears for 2008-2010 F-250 and F-350 trucks because they may not install properly, risking loss of steering control.
Blue Bird is recalling 2016 All American school buses because a steering shaft clamp may contact the rubber boot, increasing steering effort and crash risk.
Agility is recalling LNG fuel systems installed on heavy-duty vehicles in 22 states and D.C. because corroded solenoid valves may cause the vehicle to stall, increasing crash risk.
Dream on Me is recalling 2-in-1 bassinets because wire supports can disconnect, causing fabric sides to lower and posing fall and suffocation risks.
Flow Sports is recalling about 10,400 2014 Flite-series snowboard bindings because a pin can disengage, causing the binding to open and posing a fall hazard.
Honda is recalling specific 2014-2015 Accord and CR-V vehicles due to improperly torqued engine bolts that may cause power loss, oil leaks, or fire.
Prevost is recalling 455 model year 2007-2012 buses because a missing clip allows the fuel line to rub against a coolant hose, potentially causing a leak and fire.
Kia is recalling 2014-2015 Soul and Soul electric vehicles because a section of the accelerator pedal may bend and fracture, potentially causing difficulty accelerating and increasing crash risk.
Prevost is recalling 291 motorcoaches because certain fire extinguishers may not fully discharge, increasing injury risk during a fire.
Wheeled Coach is recalling 18 model year 2010 ambulances due to potential electrical issues that may cause loss of instrument panel functions and lighting.
Campos Foods is recalling approximately 126,705 pounds of H-E-B beef cheese burgers because they contain undeclared wheat, a known allergen.
Oscar's Hickory House Inc. is recalling approximately 32 pounds of beef jerky due to a processing deviation that makes the product susceptible to environmental pathogens.
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