Archive
645 recalls were announced in April 2014.
Of the 645 recalls this month scored against our rubric, 9% are Critical, 23% are Severe.
Which agencies issued them
Mrs. Rigg's Sandwiches is recalling Poor Boy and Italian Torpedo Sandwiches because they were made with meat that lacked federal inspection.
Helados La Tapatia is recalling Fresa Fruit Bars and related products because FDA environmental sampling detected Listeria monocytogenes.
Helados La Tapatia is recalling 4 oz Nuez Pecan Milk Bars because FDA environmental sampling detected Listeria monocytogenes on food contact surfaces.
Parkers Farm Inc is recalling Spicy Beer Cheese Spread due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Helados La Tapatia is recalling Jamaica Fruit Bars because FDA environmental sampling detected Listeria monocytogenes in the facility.
Helados La Tapatia is recalling 3 oz. Guava Fruit Bars because FDA environmental sampling detected Listeria monocytogenes on food contact surfaces.
Helados La Tapatia is recalling Pica de Gallo Fruit Bars because FDA environmental sampling found Listeria monocytogenes on food contact surfaces.
Parkers Farm Inc is recalling Fire Roasted Salsa due to potential Listeria monocytogenes contamination. Consumers should check sell-by dates and stop using the product.
Helados La Tapatia is recalling 4-ounce Limon Bolis ice cream because FDA environmental sampling detected Listeria monocytogenes on food contact surfaces.
Autocar is recalling 2012-2014 Xpert vehicles because floor mats may have prevented proper seat bolt tightening, increasing injury risk in crashes.
Helados La Tapatia is recalling Vanilla Milk Bars and ice cream containers after FDA environmental sampling detected Listeria monocytogenes.
GE Healthcare is recalling 453 OEC 9900 Elite mobile fluoroscopy systems because defective screws may cause the workstation monitor to fall forward.
Highland Ridge RV is recalling 2014 Open Range LF319 fifth wheel trailers because a short gas line may leak when the kitchen slideout is expanded, increasing fire risk.
Helados La Tapatia is recalling Cappuccino 9 oz cups due to Listeria monocytogenes found in environmental sampling.
Helados La Tapatia is recalling Vainilla con Membrillo Milk Bars because FDA environmental sampling found Listeria monocytogenes in the facility.
Helados La Tapatia is recalling Lemon Lime Fruit Bars because FDA environmental sampling found Listeria monocytogenes in the facility.
Helados La Tapatia is recalling Walnut Milk Bars because FDA environmental sampling found Listeria monocytogenes in the facility.
Forest River is recalling 152 model year 2014 XLR XLT29HSF travel trailers because the Federal Certification label lists incorrect weight ratings, which could lead to tire failure.
Tedesco LLC is recalling 120/5.1 oz cups of Graeter's Cookies and Cream ice cream because the label fails to list wheat and soy allergens.
Edwards Lifesciences is recalling 28,885 Fem-Flex II Arterial and Femoral Cannulae because the dilator tips may separate.
Helados La Tapatia is recalling 3 oz Banana Milk Bars because FDA environmental sampling detected Listeria monocytogenes in the facility.
Helados La Tapatia is recalling Mango Milk Bars because FDA environmental sampling detected Listeria monocytogenes on food contact surfaces.
Helados La Tapatia is recalling Strawberry Fruit Bars because FDA environmental sampling detected Listeria monocytogenes in the facility.
Helados La Tapatia is recalling Pina Colada Milk Bars because FDA environmental sampling detected Listeria monocytogenes on food contact surfaces.
Solta Medical is recalling 1,077 Fraxel DUAL 1550/1927 Laser Systems because obsolete treatment cards may contain incorrect indications for treating Melasma.
Codman & Shurtleff is recalling 9,445 units of Certas Programmable Valves to ensure customers have tools to verify valve settings and location on x-ray images.
Gold Medal Products is recalling 11 gallons of 1031 GA Artificial Cherry Concentrate because the flavor concentration is too high.
Gold Medal Products is recalling 29 gallons of 1358 Artificial Cherry Kola flavoring because the flavor concentration is too high.
Philips is recalling 116 Ingenuity Core 128 CT systems worldwide because a software upgrade caused intermittent reconstruction failures.
Terumo is recalling 37 units of Cardiovascular Procedure Kits in California due to an incorrect customer notification label applied to the Tyvek lid.
Gold Medal Products is recalling 2521 Cherry Glaze Pop popcorn flavoring because the flavor concentration is too high. The product was distributed in 17 states.
Gold Medal Products is recalling 327 Ace Cherry Berry Flossugar because the flavor concentration is too high. The product was distributed in 17 states.
Magno Humphries Laboratories is recalling Vitamin E softgels because the main label states 1000 IU while the Supplement Facts panel indicates 200 IU.
Kellogg's Eggo Buttermilk waffles are being recalled in Canada due to the potential presence of small plastic pieces in the product.
Ortho-Clinical Diagnostics is recalling VITROS CRBM Slides, Lot 3920-0080-8403, because they may produce biased carbamazepine results.
Synthes is recalling CMF Battery Powered Drivers because the packaging graphics suggest off-label use with taps, which is not intended.
Synthes, Inc. is recalling 20 Hohmann retractors because they were mis-etched with the wrong part number.
MTD is recalling Troy-Bilt electric leaf blowers because the impeller can break and strike the operator, posing a laceration hazard.
E-Z-GO is recalling approximately 30,000 golf, shuttle, and off-road utility vehicles because an insufficiently tightened steering wheel nut may reduce steering control.
Grand Design is recalling 2014 Solitude fifth wheel travel trailers equipped with certain Frigidaire microwaves that may start on their own and cause a fire.
Excalibur is recalling about 1,000 Matrix Mega 405 crossbows because they can fire unexpectedly without the trigger being pulled, posing an injury risk.
MTD is recalling Remington electric leaf blowers because the impeller can break and strike the operator, posing a laceration hazard.
Gillig LLC is recalling 98 aftermarket accelerator pedals where mechanical springs may break, preventing the pedal from returning to idle and increasing crash risk.
Kraft Foods Group is recalling approximately 96,000 pounds of Oscar Mayer Classic Wieners because the packages may contain cheese dogs with undeclared milk.
Gold Creek Foods is recalling approximately 24,000 pounds of fully cooked breaded chicken breast products because they contain undeclared egg and wheat allergens.
BMW is recalling 2013 R 1200 GS motorcycles because transmission pressure may push the output seal out of place, causing oil to leak onto the rear tire and increasing crash risk.
Federal Corporation is recalling specific Couragia A/T tires due to steel belt separation that can cause shoulder cracks and loss of pressure.
Mack is recalling 2014-2015 Pinnacle trucks because a missing pressure relief valve could cause the air tank to rupture, increasing injury risk.
Mack Trucks is recalling 2010-2015 CXU trucks because exhaust pipes may block rear reflectors, reducing visibility and increasing crash risk.
Prevost is recalling 80 X3-45 and H3-45 coaches because raised wheelchair seats may damage seat belts, increasing injury risk in a crash.
E-One is recalling 112 model year 2013-2014 Typhoon, Quest, and Cyclone II fire fighting chassis because a software defect may cause brake lights to stay on or prevent idle raise.
Mack Trucks is recalling certain 2007-2014 models because the hazard warning lights may fail, reducing visibility and increasing crash risk.
Alliance Tire Americas is recalling specific 14-17.5 ML Alliance 239 tires because they lack required sidewall markings, which could lead to overloading and blowouts.
Navistar is recalling certain 2013-2015 International DuraStar, WorkStar, ProStar, and TranStar trucks because brake caliper bolts may be missing or improperly torqued, increasing crash risk.
Ford is recalling 2015 F-250, F-350, F-450, and F-550 Super Duty trucks because a software error may cause the vehicle to briefly engage Reverse when Drive is selected.
Double K is recalling 2009-2010 Hometown Trolley Villager and Mainstreet models because voltage spikes may cause electrical components to overheat, increasing the risk of a fire.
Ontel is recalling about 170,000 ISO7X isometric exercise devices because handle grips can break and eject parts, posing an injury risk.
BMW is recalling 2014 X5 vehicles because rear door child safety locks may disengage, allowing rear occupants to open doors while the vehicle is in motion.
Isuzu is recalling 2012-2013 Reach stripped chassis because the horn switch may fail, increasing crash risk. Dealers will inspect and replace the switch free of charge.
Pier 1 Imports is recalling hanging glass star lanterns because solder welds can melt from tea light heat, posing a fire hazard. No injuries have been reported.
Rocky Brands is recalling about 6,800 Georgia Boot steel-toed work shoes because the steel toe cap may fail to protect feet when compressed. No injuries have been reported.
Bolzano Artisan Meats is recalling approximately 5,723 pounds of salami products because they were misbranded with the USDA Mark of Inspection without federal authorization.
Vermont Common Foods is recalling Orton Bros. Zesty Lemon Cookie Buttons because they contain undeclared peanuts. The recall affects 1,188 boxes distributed in New England.
Delhaize America (Hannaford Bros) is recalling St. Mary's River Smokehouses Oven Smoked Atlantic Salmon Stix, Chili Mango Flavor, due to potential Listeria monocytogenes contamination.
The FDA is recalling Vicerex male sexual enhancer capsules because laboratory analysis found undeclared tadalafil, an unapproved drug ingredient.
Zions RX Formulations is recalling 450 vials of Calcium Gluconate 10% for Injection due to a report of microbial contamination.
Slim Beauty USA is recalling Dr. Ming's Chinese Capsule because it contains undeclared sibutramine and phenolphthalein, making it an unapproved new drug.
Slim Beauty USA is recalling Dream Body Slimming Capsules because they contain undeclared sibutramine, an unapproved new drug not currently marketed in the United States.
Slim Beauty USA is recalling Magic Slim capsules nationwide because they contain undeclared sibutramine and phenolphthalein, making them unapproved new drugs.
Terra-Medica Inc. is recalling specific batches of Pleo Not Ointment because of penicillin cross contamination. The product was distributed in the US, Canada, and the Philippines.
Command Nutritionals LLC is recalling Hard Blast and Juggernaut products because they contain contaminated L-Citrulline.
The FDA is recalling Black Ant dietary supplements because laboratory analysis found they contain undeclared sildenafil, an FDA-approved drug for erectile dysfunction.
Terra-Medica Inc. is recalling Pleo Fort Suppositories because of penicillin cross-contamination. The product was distributed in the US, Canada, and the Philippines.
Nature's Value Inc. is recalling Vitacost Men's Passion Booster because the L-Citrulline ingredient contained an unidentified compound.
Terra-Medica Inc. is recalling Pleo Fort Tablets 5X due to penicillin cross-contamination. The product was distributed nationwide and internationally.
Terra-Medica Inc. is recalling Pleo Quent capsules due to penicillin cross-contamination. The product was distributed in the US, Canada, and the Philippines.
Terra-Medica Inc. is recalling Pleo-Fort DROPS 5X homeopathic medicine due to penicillin cross-contamination. The product was distributed in the US, Canada, and the Philippines.
Draeger Medical Systems is recalling three Oxylog 3000 plus ventilators because the control knobs may interrupt contact, causing the device to stop ventilation.
Terra-Medica Inc. is recalling Pleo Not Suppositories 3X due to penicillin cross-contamination. The affected homeopathic medicine was distributed in the US, Canada, and the Philippines.
Zions RX Formulations is recalling 861 bags of Magnesium Sulfate in Lactated Ringers due to poor aseptic practices that compromise sterility assurance.
Terra-Medica Inc. is recalling Pleo Quent homeopathic medicine because of penicillin cross-contamination. The product was distributed in the US, Canada, and the Philippines.
Nissan is recalling 2014 Leaf vehicles because missing welds on the front structural member may reduce crash protection. Owners should contact a dealer for a free inspection and repair.
Zions RX Formulations is recalling 95 vials of Potassium Phosphates due to a lack of assurance of sterility caused by poor aseptic practices.
Terra-Medica Inc. is recalling Pleo Fort Portable Sips homeopathic medicine because of penicillin cross-contamination. The products were distributed in the US, Canada, and the Philippines.
Zions RX Formulations is recalling 60 units of Bupivacaine 3% in Arizona due to poor aseptic practices that compromised sterility assurance.
Pega Medical Inc. is recalling five units of the Fassier-Duval IM Telescopic System because the male components were made with material of lower strength than specifications.
Terra-Medica Inc. is recalling specific batches of Pleo Stolo DROPS 6X homeopathic medicine due to penicillin cross-contamination. Consumers should stop using the product and contact the company for a refund.
Terra-Medica Inc. is recalling Pleo Ex DROPS 5X homeopathic antifungal medicine due to penicillin cross-contamination. The product was distributed in the US, Canada, the Philippines, and online.
Terra-Medica Inc. is recalling specific batches of Pleo Not DROPS homeopathic medicine due to penicillin cross contamination. The product was distributed in the US, Canada, and the Philippines.
Terra-Medica Inc. is recalling Pleo Nota-Quent Drops because of penicillin cross-contamination. The product is distributed in the US, Canada, and the Philippines.
Terra-Medica Inc. is recalling Pleo Quent Suppositories 3X due to penicillin cross-contamination. The product was distributed in the US, Canada, and the Philippines.
Terra-Medica Inc. is recalling specific batches of Pleo Ex Portable Sips homeopathic medicine due to penicillin cross-contamination.
Terra-Medica Inc. is recalling Pleo Not Portable Sips oral homeopathic medicine due to penicillin cross-contamination. The products were distributed in the US, Canada, and the Philippines.
Terra-Medica Inc. is recalling specific batches of Pleo Quent DROPS 5X oral homeopathic medicine due to penicillin cross contamination.
Terra-Medica Inc. is recalling specific batches of Pleo Not Portable Sips oral homeopathic medicine because of penicillin cross-contamination.
Zions RX Formulations Services LLC is recalling specific lots of Vitamin B-12 injections due to a lack of assurance of sterility resulting from poor aseptic practices.
Zions RX Formulations is recalling 1,495 bags of Oxytocin 30 Units in 500mL Sodium Chloride 0.9% due to a lack of assurance of sterility.
Glenmark Generics Inc. is recalling specific bottles of Ranitidine Tablets USP 150 mg because they were found to contain foreign Metoprolol Tartrate tablets.
Terra-Medica Inc. is recalling Pleo Not Tablets 5X because of penicillin cross contamination. The affected homeopathic medicine was distributed in the US, Canada, and the Philippines.
Zions RX Formulations is recalling 610 units of Sodium Bicarbonate 8.4% injectable products due to a lack of assurance of sterility.
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