Consumer Product recall alerts and consumer safety news updated hourly http://www.recallowl.com/Household+Recalls/Consumer+Products Thu, 27 Feb 2014 14:08:21 +0100 http://www.recallowl.com/images/rss.gif http://www.recallowl.com The feed is managed/created by RecallOwl.com (http://www.recallowl.com). http://www.recallowl.com/Household+Recalls/Consumer+Products/MyNicKnaxs%2C+LLC.++Issues+a+Voluntary+Nationwide+and+International+Recall+of+All+Weight+Loss+Formulas+of+Reduce+Weight+Fruta+Planta ... Thu, 13 Feb 2014 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/The+Mentholatum+Company+Issues+Voluntary+Nationwide+Recall+of+Rohto%26%23174%3B+Eye+Drops+Made+in+Vietnam - Orchard Park, NY - January 16, 2014 - The Mentholatum Company announced today it is conducting a voluntary recall to the retail level of RohtoŽ Arctic, RohtoŽ Ice, RohtoŽ Hydra, RohtoŽ Relief and RohtoŽ Cool eye drops Made in Vietnam. This recall includes ONLY lots of product that were manufactured in Vietnam and DOES NOT include eye drops made in Japan. The lot numbers for products made in Vietnam will ... Thu, 16 Jan 2014 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Midwest+Wholesale+Issues+Voluntary+Recall+of+Boost+Ultra%2C+XZone+Gold%2C+Sexy+Monkey%2C+Triple+MiracleZen+Platinum%2C+Magic+for+Men%2C+%22New%22+Extenze%2C+and+New+XZen+Platinum+Marketed+as+a+Dietary+Supplements+Due+to+the+Presence+of+Undeclared+Drug+Ingredients - January 9, 2014 - Nixa, MO, Midwest Wholesale is voluntarily recalling the following products and Lot numbers. List of Products included in this Recall: Boost Ultra 12 pill bottle, Lot#B70130, Exp 03/15 3 pill bottle, Lot#B70130, Exp 3/2015 1 pill pack, Lot#06012011, Exp 6/2014 XZone Gold 1 pill pack, Lot#130710GL, Exp 7/31/18 Sexy Monkey... Fri, 10 Jan 2014 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Tendex+Issues+Voluntary+Nationwide+Recall+of+P-Boost%2C+NatuRECT+Due+to+Undeclared+Active+Ingredients - November 19, 2013 - Los Angeles, CA Tendex is voluntarily recalling Lot# F51Q of P-Boost and Lot # F51Q of NatuRECT to the consumer level. FDA laboratory analysis on Lot# F51Q of P-Boost, which the firm also labels as NatuRECT, has determined that this product contains undeclared tadalafil. Tadalafil is an active ingredient of FDA-approved drugs used to treat erectile dysfunction (ED), making these products unapproved drugs. The undeclare... Wed, 20 Nov 2013 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Jobbers+Wholesale+Issues+Voluntary+Recall+of+Rhino+5+Plus%2C+Maxtremezen+and+Extenzone+Marketed+as+a+Dietary+Supplement+Due+to+the+Presence+of+Undeclared+Drug+Ingredients - November 16, 2013 - Paramount, CA, Jobbers Wholesale is voluntarily recalling Lot No. KWAKPMC030505175957019 of Rhino 5 Plus, Lot No. JBP-L-1270-70 of Maxtremezen and Lot No. KWAKPMC03050517 of Extenzone to the consumer level. FDA analysis found these products to contain undeclared desmethylcarbondenafil and dapoxetine. Desmethylcarbondenafil is a phosphodiesterase PDE-5 inhibitor which is a class of drugs used to treat male erectile dysfunctio... Mon, 18 Nov 2013 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Afikim+Electric+Vehicles+Issues+Nationwide+Recall+of+Breeze+C+Scooter - September 27, 2013 - On September 27, 2013, Afikim Electric Vehicles initiated a nationwide recall of 69 Breeze C Scooters. The Breeze C Scooter may become unresponsive during operation due to an electrical contact which may fault due to extensive wear, which potentially could result in the driver not being able to stop the scooter during operation except by turning off the ignition key. There is a Correction in process which has been rep... Mon, 30 Sep 2013 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Carefusion+Provides+Update+On+Voluntary+Recall+Of+Avea%26reg%3B+Ventilator - September 30, 2013 - CareFusion issued the following update regarding its previously announced voluntary recall of AVEAŽ ventilators. The company initiated the voluntary recall on Sept. 3, 2013. The FDA has classified this action as a Class I recall. A Class I recall is defined as a reasonable probability of serious adverse health consequences or death associated with use of the defective units. CareFusion anno... Mon, 30 Sep 2013 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/W.S.+Badger+Company+Voluntarily+Recalls+Select+Lots+of+Daily+SPF+30+Kids+%26+Baby+Sunscreen+Lotions+Due+to+Microbial+Contamination - September 23, 2013 - W.S. Badger Co. Inc. today announced it is voluntarily recalling all lots of its 4-ounce SPF 30 Baby Sunscreen Lotion and one lot of its 4-ounce SPF 30 Kids Sunscreen Lotion (lot # 3164A) due to microbial contamination. The products were tested and found to be contaminated with Pseudomonas aeruginosa, Candida parapsilosis and Acremonium fungi. No adverse reactions have been reported in connection with thes... Wed, 25 Sep 2013 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Volcano+Company%2C+Issues+Voluntary+Worldwide%2FNationwide+Recall+of+Volcano+Male+Enhancement+Liquid+and+Volcano+Male+Enhancement+Capsules%2C+Marketed+as+a+Dietary+Supplement%2C+Due+to+Undeclared+Active+Ingredients - July 18, 2013 - Long Beach, CA, Volcano Company is voluntarily recalling all lots of Volcano Male Enhancement Liquid and Volcano Male Enhancement Capsules to the consumer level. FDA test results revealed the Volcano Male Enhancement Liquid has been found to contain undeclared Desmethyl Carbodenafil, Dimethylsildenafil, and Dapoxetine. FDA test results revealed Volcano Capsules have been found to contain undeclared Desmethyl Carbodenafil and Dap... Fri, 19 Jul 2013 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Beamonstar+Products+Issues+Voluntary+Nationwide+Recall+of+SexVoltz%2C+Velextra%2C+%26+Amerect+Marketed+as+a+Dietary+Supplement%2C+Due+to+Undeclared+Active+Ingredients-+Expanded+to+Include+SexVoltz+12+Capsules+Bottle%2C+SKU+626570615316. - May 10, 2013 -Queen Creek, AZ, BeaMonstar Products is voluntarily recalling all of SexVoltz brand SKU's 626570609490, 827912089028, 626570617877, 626570615316, 626570615316 Velextra brand SKU's 626570613855, 626570619055, 626570617860, 626570617563 Amerect SKU's 626570619031, 626570619628 capsules to the consumer level. Laboratory analysis conducted by the FDA on SexVoltz and Velextra has determined these products contain undeclared tadalafil. ... Fri, 10 May 2013 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Bimeda+Inc.+on+Behalf+of+Manufacturer+Bimeda-MTC+Animal+Health+Inc.+Issues+Voluntary+Nationwide+Recall+of+Sterile+Solutions+Due+to+Concerns+Regarding+Sterility+and+Possible+Health+Risk - May 2, 2013 - Bimeda Inc., on behalf of the manufacturer, Bimeda-MTC Animal Health Inc. is voluntarily recalling one lot of Calcium Gluconate, one lot of Dextrose 50%, and one lot of Hypertonic Saline, all of which are in the form of injectable fluids, to the user level. These injectable fluids are being recalled as a precautionary measure; because of departures from customary sterility procedures, sterility cannot be entirely assured. Th... Thu, 09 May 2013 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Medtronic+Announces+FDA+Classification+Of+Deep+Brain+Stimulation+Lead+Cap+Communication - May 2, 2013 - In keeping with its commitment to keep physicians informed about product performance and safety, Medtronic, Inc. (NYSE: MDT) issued an Urgent Medical Device Correction notification in February 2013 to provide physicians with information concerning the potential for deep brain stimulation (DBS) lead damage associated with the use of the lead cap provided in Medtronic DBS lead kits and dystonia therapy kits. The U.S. Food and Drug A... Fri, 03 May 2013 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Freedom+Trading+Issues+a+Voluntary+Nationwide+Recall+of+Super+Power%2C+a+Product+Marketed+as+a+Dietary+Supplement+to+Support+Male+Sexual+Performance%2C+Due+to+Undeclared%2C+Potentially+Hazardous++Active+Ingredient - January 24, 2013 - Woodbridge, NJ - D&S Herbals, LLC, d/b/a Freedom Trading is conducting a voluntary consumer recall of a product sold as a dietary supplement under the brand name of Super Power. This product was sold between August 2012 and January 2013 nationwide. Finished product of Super Power was tested and found to contain trace amounts of an FDA-approved drug. Analytical tests conducted by independent labs of Super Power concl... Mon, 28 Jan 2013 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Energizer+Holdings+Inc.%2C+Announces+the+Voluntary+Nationwide+Market+Withdrawal+of+several+Banana+Boat+Sun+Care+Products - October 19, 2012 - Energizer Holdings Inc. (NYSE: ENR) (St. Louis, MO), announced today it is initiating a voluntary market withdrawal of the continuous spray Banana Boat sun care products identified in the table below due to a potential risk of product igniting on the skin if contact is made with a source of ignition before the product is completely dry.... Fri, 19 Oct 2012 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Stryker+Issues+Class+1+Recall+of+Neptune+Rover+Waste+Management+System+in+the+United+States%2C+Asia+Pacific%2C+Canada%2C+Japan%2C+Latin+America+and+EMEA September 25, 2012 - On June 5, 2012, Stryker initiated a Class 1 recall of the Neptune Waste Management System. The devices are being recalled because Stryker has received two reports of serious injury as a result of tissue damage associated with the use of the Neptune 2, including an event in which one customer connected the Neptune 2 System to a passive chest drainage tube post operatively, resulting in a fatality. The recall includes al... Tue, 25 Sep 2012 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/CRM+Laboratories+Issues+a+Voluntary+Nationwide+Recall+of+X-ROCK+3+Day+Pill+For+Men+and+Z-ROCK+All+Natural+Male+Supplement+Products+Marketed+as+Dietary+Supplements+to+Support+Male+Sexual+Performance+Due+to+Undeclared+Active+Ingredients - July 20, 2012 - CRM Laboratories is conducting a consumer/user level recall of all X-ROCK 3 Day Pill For Men and Z-ROCK products sold between October, 2011 and April, 2012. Finished product of X-ROCK 3 Day Pill for Men and Z-ROCK was tested and found to contain an analogue of an ingredient in an FDA-approved drug. Analytical tests conducted by the Food and Drug Administration (FDA) concluded that the products contained sildenafil and h... Tue, 24 Jul 2012 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Westone+Laboratories+Inc.+Issues+Voluntary+Nationwide+Recall+of+all+sizes+and+packaging+configurations+of+Oto-Ease+ear+lubricant+due+to+possible+microbial+contamination. - July 13,2012, Westone Laboratories, Inc. is initiating a voluntary nationwide recall of all sizes and packaging configurations of Oto-EaseŽ ear lubricant. The products have been found through a consumer complaint and the U.S. Food and Drug Administration (FDA) sample analysis to be potentially contaminated with pathogenic bacteria and mold. Use of the product as directed for easing the insertion of custom fit ear molds and hearing instruments (... Fri, 13 Jul 2012 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Sandoz+US+Announces+Precautionary+Recall+Of+Oral+Contraceptive+Introvale%26reg%3B%2C+Following+Report+Of+Packaging+Flaw - June 5, 2012 - Sandoz is conducting a voluntary recall of 10 lots of its generic oral contraceptive IntrovaleŽ in the US, following a recent report of a packaging flaw. The probability of this packaging flaw causing serious adverse health consequences is remote and Sandoz is not aware of any reports of related adverse events. This recall is being undertaken as a precautionary measure to minimize any potential of patients being impacted. The rec... Wed, 06 Jun 2012 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Hocean+Inc.+Recalls+Nitre+Power+4oz+Plastic+Bags+Because+of+Possible+Health+Risks - May 25, 2012 - HOCEAN, INC. of Commerce City, CA is recalling all Nitre Powder 4oz plastic bags with UPC 0 45027 97918 2, because it has the potential to be contaminated with higher levels of sodium nitrite. Consumption of hazardous amounts of sodium nitrites can lead to life-threatening illness and/or death. Nitre Powder was distributed to Asian food markets and other grocery stores from July 2008 to Fe... Fri, 25 May 2012 07:00:00 +0100 http://www.recallowl.com/Household+Recalls/Consumer+Products/Regeneca%2C+Inc.+Issues+A+Voluntary+Nationwide+Recall+Of+A+Specific+Lot+Of+RegenArouse+Because+Of+Potential+Health+Risks - February 10, 2012 - Regeneca, Inc. announced today that it is conducting a voluntary nationwide recall of RegenArouse, Lot Number 130100, because FDA lab analysis has confirmed the presence of Tadalafil making these products unapproved new drugs. Tadalafil is an FDA-approved drug used as treatment for male Erectile Dysfunction (ED). The active drug ingredient is not listed on the label for these products. Use of these products may pose a ... Sat, 11 Feb 2012 07:00:00 +0100