Archive
854 recalls were announced in March 2017.
Of the 854 recalls this month scored against our rubric, 11% are Critical, 25% are Severe.
Which agencies issued them
Polaris is recalling 2017 Slingshot, SL, and SLR vehicles because three steering and suspension bolts may be insufficiently tightened, potentially reducing vehicle handling.
Kia is recalling 2017 Niro Hybrid vehicles because a damaged steering connector may cause a loss of power steering assist, increasing the risk of a crash.
R.W. Beckett is recalling approximately 18,000 Firomatic fusible safety valves because the stem may fail to seal, allowing fuel to leak and posing a fire hazard.
Gillig is recalling 2,732 Low Floor transit buses because wiper arms can crack and detach, reducing driver visibility and increasing crash risk.
Jaguar is recalling 2017 F-PACE vehicles with automatic transmissions because a short rear driveshaft may separate, causing loss of drive power and increasing crash risk.
King's Command Foods is recalling approximately 26,138 pounds of ground beef products due to possible contamination with extraneous materials, including metal objects.
Jaguar Land Rover is recalling 2016 Range Rover and Range Rover Sport vehicles because the passenger air bag inflator may fail to ignite, preventing deployment in a crash.
Airstream is recalling 2017 Base Camp recreational trailers because heavy loads may cause tires to contact the wheel well liner, risking tire failure and crashes.
Picone Meat Specialties is recalling approximately 5,750 pounds of pork salami products because they contain non-fat dry milk, a known allergen, that is not declared on the label.
RDG Global is recalling about 2,600 girls' hooded sweatshirts sold at Nordstrom because the hood drawstrings pose a strangulation hazard to children.
Manac is recalling 2016-2017 Van Trailers because aluminum rivets securing external rub rails may fail, allowing the rails to detach and become road hazards.
Pier 1 Imports is recalling Neely and Dahlia bistro chairs because loose bolts can cause the legs to collapse, posing a fall hazard.
Shearers Foods is recalling Delish Jalapeno White Cheddar Potato Chips because ingredients from Valley Milk Product may be contaminated with Salmonella.
Tasty Delicious Bakery Inc. is recalling Sugar Buns due to undeclared eggs, milk, and food dyes. The product was distributed in New York and New Jersey.
Altijira Murray Products, LLC is recalling Foxy's Salted Caramel and English Toffee due to potential Listeria monocytogenes contamination. The product was distributed in California and New York.
United Exchange Corporation is recalling 46,080 bottles of Eye Wash due to direct evidence of non-sterility contamination in two lots.
The Kroger Co. is recalling Fred Meyer 100% Whole Wheat Bread because it may contain undeclared milk.
Shearers Foods is recalling Deep River Sour Cream & Onion Krinkle Kettle Chips because ingredients from Valley Milk Product may be contaminated with Salmonella.
Altijira Murray Products, LLC is recalling Foxy's Uncle Mike's Double Chocolate ice cream due to potential Listeria monocytogenes contamination.
Altijira Murray Products, LLC is recalling foxy's rather thoughtful vanilla 1 Pint ice cream due to potential Listeria monocytogenes contamination. The product was distributed in California and New York.
Pacific Medical Solutions is recalling Nano PNC Water because it was marketed without FDA approval and tested positive for the bacterium variovorax paradoxus.
Papa John's Salads & Produce, Inc. is voluntarily recalling Co-Jack Cheese Half Moons because they may be contaminated with Listeria monocytogenes.
Shearers Foods is recalling Larry The Cable Guy Biscuits & Gravy Thin Potato Chips because ingredients may be contaminated with Salmonella.
Altijira Murray Products, LLC is recalling Foxy's Oregon Cherry Vanilla 1 Pint ice cream due to potential Listeria monocytogenes contamination. The product was distributed in California and New York.
Chip 'n Dipped is recalling 63% Cacao Dark Chocolate due to the presence of an undeclared milk allergen. The product was distributed to retail stores in New York, Pennsylvania, and Massachusetts.
Jeffreys Drug Store is recalling compounded Domperidone capsules 10 mg because the product was marketed without an approved NDA/ANDA, meaning safety and efficacy have not been established.
Shearers Foods is recalling Spicy Nacho Cheese Tortilla Chips because ingredients from Valley Milk Product may be contaminated with Salmonella.
Shearers Foods is recalling specific bags of nacho cheese tortilla chips because they contain ingredients from a supplier that may be contaminated with Salmonella.
Snak King Corporation is recalling specific lots of Cashew Clusters 32 oz because they may be contaminated with Salmonella.
Altijira Murray Products, LLC is recalling Foxy's California Pistachio 1 Pint due to potential Listeria monocytogenes contamination. The product was distributed in California and New York.
Papa John's Salads & Produce is voluntarily recalling Monterey Jack Cheese Half Moons due to possible Listeria monocytogenes contamination.
Olympus is recalling URF-P6 and URF-P6R uretero-reno fiberscopes due to adverse events involving tissue trauma and stuck insertion tubes reported in similar devices.
Hyundai is recalling 2011-2015 Sonata and Sonata Hybrid vehicles because front seat belt linkages may detach from anchor pretensioners, increasing injury risk in crashes.
Volkswagen is recalling 2007-2010 Touareg vehicles because a fuel filter flange may crack and leak fuel, increasing the risk of fire.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
ADM Milling Co. is recalling 25,000 pounds of ADM Polar Bear Flour because a product sample tested positive for salmonella. The flour was distributed in Illinois and Indiana.
Papa John's Salads & Produce is voluntarily recalling Colby Cheese Half Moons due to possible Listeria monocytogenes contamination.
JML Ingredients is recalling IQF Cut Green Beans in 20 lb cases due to potential Listeria monocytogenes contamination. The product was distributed in Massachusetts and Pennsylvania.
United Exchange Corporation is recalling 112,320 bottles of Eye Irrigating Solution because the product lacks assurance of sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.
Sunrise Growers is recalling organic IQF Dark Sweet Cherries due to possible Listeria monocytogenes contamination. The recall covers 1,800 cases distributed in California.
Mylan Pharmaceuticals is recalling 1,338 bottles of Glipizide 5 mg Extended-Release Tablets because they may contain 10 mg tablets.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in AMS kits are recalled because splits or holes may compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions arthroscopy kits are recalled because splits or holes may compromise sterility.
United Exchange Corporation is recalling 77,184 bottles of Eye Wash because the product lacks assurance of sterility. The recall covers specific lots distributed nationwide, in Puerto Rico, and in Guyana.
United Exchange Corporation is recalling 190,710 bottles of Eye Wash due to a lack of assurance of sterility. The product was distributed nationwide, in Puerto Rico, and in Guyana.
G&W Laboratories is recalling Indocin suppositories due to out-of-specification impurity results found during stability testing.
Papa John's Salads & Produce is voluntarily recalling Pepper Jack Cheese Half Moons due to possible Listeria monocytogenes contamination.
Olympus is recalling URF-V2 and URF-V2R endoscopes because the insertion tube bending section may break during surgery, causing tissue trauma.
AbbVie is recalling Duopa (carbidopa and levodopa) cassettes because stability testing showed the drug may settle near the end of its shelf life.
Windstone Medical Packaging is recalling 606 Shoulder Arthroscopy Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
Cook Inc. is recalling 1,875 TriForce Peripheral Crossing Sets because a specific valve design is associated with increased reports of blood loss.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Windstone Medical Packaging is recalling 66 C-Tray Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
Windstone Medical Packaging is recalling Medtronic disposable gloves in custom kits because splits or holes may compromise sterility.
Windstone Medical Packaging is recalling 365 Minor Procedure Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Windstone Medical Packaging is recalling Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom kits because splits or holes may compromise sterility.
Synthes (USA) Products LLC is recalling two PRODISC Orthopedic Manual Surgical Instrument struts used in spinal surgery because they are incorrectly etched and labeled with the wrong size.
Windstone Medical Packaging is recalling 276 Basic Setup Packs because the Medtronic gloves inside may have splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 561 pacemaker kits because the disposable gloves included may contain splits or holes that compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.
Maquet is recalling Li-Ion batteries for CARDIOSAVE IABP devices after reports of venting when dropped.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Windstone Medical Packaging is recalling 390 ENT Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 1,081 arthroscopy kits because the disposable gloves inside may have splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 123 Lumbar Laminectomy Packs because the included gloves may have splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 1,125 Open Procedure Packs because the disposable gloves included may have splits or holes that compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom AMS kits are recalled because splits or holes may compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Beckman Coulter is recalling iChemVELOCITY Urine Chemistry Systems because probe misalignment or bending can lead to delayed or incorrect patient results.
Windstone Medical Packaging is recalling 174 Angio Pack kits because the Medtronic gloves inside may have splits or holes that compromise sterility.
Gamay Foods Inc is recalling Original Cheddar Cheese Seasoning because a milk powder ingredient was recalled for potential Salmonella contamination.
Fred Meyer is recalling Bakery Fresh Goodness Carrot Cupcakes because they contain undeclared milk and soy.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Windstone Medical Packaging is recalling 225 Lap Gallbladder Packs because the included Medtronic gloves may have splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 88 surgical packs because the gloves inside may have splits or holes that compromise sterility.
Phadia US Inc is recalling EliA Sample Diluent because liquid level detection problems in Phadia 250 instruments caused erroneous test results.
Windstone Medical Packaging is recalling 1,436 breast augmentation kits because the disposable gloves included may contain splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 875 Shoulder Pack kits because the included Medtronic gloves may contain splits or holes that compromise sterility.
Cook Inc. is recalling 884 Check-Flo Performer Introducers because a specific valve design is associated with increased reports of blood loss.
Windstone Medical Packaging is recalling 2,018 Podiatry Packs because the disposable gloves included may have splits or holes that compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in AMS kits are recalled because splits or holes may compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom AMS kits are recalled because splits or holes may compromise sterility.
Windstone Medical Packaging recalled 286 Spine Pack kits because the disposable gloves may contain splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 944 Dr. Landi EVLT Packs because the included Medtronic gloves may have splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 810 Extremity Packs because the disposable gloves inside may contain splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 664 Ortho Minor Packs because the included disposable gloves may contain splits or holes that compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.
Windstone Medical Packaging is recalling 700 knee arthroscopy packs because the disposable gloves included may have splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 229 Custom Breast Augmentation Packs because the included gloves may have splits or holes that compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom kits are recalled because splits or holes may compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Cook Inc. is recalling 41,975 Flexor Radial Access Sets because a specific hemostatic valve design is associated with increased reports of blood loss.
Cook Inc. is recalling 29 Check-Flo Introducer Hausdorf-Lock Atrial devices worldwide due to increased reports of blood loss associated with the hemostatic valve design.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom kits are recalled because splits or holes may compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom kits are being recalled because splits or holes may compromise sterility.
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