WEEK ENDING MAY 26
WEEK ENDING MAY 19
WEEK ENDING MAY 5
Church & Dwight Co., Inc. is recalling Spinbrush® Rechargeable SONIC toothbrushes because the charging base may overheat with localized melting and sparking, possibly causing fire, shock or burns.
The recall is limited to select lots of Spinbrush® Rechargeable SONIC toothbrushes. Product with a lot number from one of the following ranges is affected by this recall: DD9310 to 9365 or DD0002 to 0122. The lot number can be found on the bottom of the charging base and on the packaging.
The indicated lots were distributed between February 2010 and October 2011 in all U.S. states and in Canada.
Consumers who have the affected units should stop using them and return them to Church & Dwight for a full refund. Consumers should call 1-888-709-4100 from 9:00 a.m. and 5:00 p.m. EDT, Monday through Friday (an automated service is available 24 hours a day or visit online at www.sonicrechargereturn.com for further information and to determine if they have product subject to this recall).
WEEK ENDING FEBRUARY 25
WEEK ENDING JANUARY 28
Johnson & Johnson Consumer Companies, Inc. is recalling from retailers one lot of AVEENO® BABY CALMING COMFORT® LOTION (full product details below) in Alabama, Arkansas, Florida, Georgia, Kansas, Louisiana, Mississippi, Tennessee and Texas.
This recall is being initiated after a test indicated that the lot exceeded the specifications for common bacteria.
Consumers who would like a refund or coupon, or who have questions or concerns about the recalled product, should call our Consumer Call Center at 1-877-298-2525 (available Monday-Friday 8 a.m. to 8 p.m. Eastern Time).
The lot number and UPC code for the recalled product is embossed on the tube.
FULL RECALLED PRODUCT LIST:
|PRODUCT NAME||LOT NUMBER||UPC CODE|
|AVEENO® BABY CALMING COMFORT® LOTION||0161LK||38137-0036456|
WEEK ENDING JANUARY 21
Perfect Image Solutions, LLC is
recalling all lots of Men's Minoxidil 15% Azelaic 5% Hair regrowth topical,
60mL; Men's Minoxidil 10% Azelaic 5% Hair regrowth topical, 60mL; Men's
Minoxidil 5% Azelaic 5% Hair regrowth topical, 60mL; Women's Minoxidil 3%
Azelaic 5% Hair regrowth topical, 60mL; and Hair regrowth shampoo enhanced with
Ketoconazole and salicylic acid, 180mL, to the consumer level. The products are
deemed “unapproved new drugs” under the law and U.S. Food and Drug
Administration regulations and may present potential health hazards.
These products are used to slow or stop hair loss and promote hair regrowth and are packaged in glass-dropper containers or plastic shampoo bottles, and are sold in single units. They are used by men and women generally in middle to late adulthood. The affected product lots include the following lot numbers and expiration dates:
|Product Name||Lots||Expiration||UPC Number|
|Men's Minoxidil 15% Azelaic 5% Hair regrowth topical, 60mL.||All||Up until Oct. 2013||736211275813|
|Men's Minoxidil 10% Azelaic 5% Hair regrowth topical, 60mL.||All||Up until Oct. 2013||736211276018|
|Men's Minoxidil 5% Azelaic 5% Hair regrowth topical, 60mL.||All||Up until Sept. 2014||736211276117|
|Women's Minoxidil 3% Azelaic 5% Hair regrowth topical, 60mL.||All||Up until Nov. 2013||736211274519|
|Hair regrowth shampoo enhanced with Ketoconazole and salicylic acid, 180mL.||All||Up until Dec. 2013||736211276414|
USA Far Ocean Group Inc. (U.S.A. Far Ocean), is recalling the Company's two products sold as cosmetic under the names Vagifresh Ball and Vagifresh Gel. These two products were also sold under the mixed package named Female One, which contained Vagifresh Ball, Vagifresh Gel and Vagifresh Liquid (this recall does not involve Vagifresh Liquid).
Lab analysis of Vagifresh Gel sample found the product contains benzocaine, the active ingredient for many anesthetic drug products. In addition, analysis of Vagifresh Ball sample found the product contains bacteria including Staphylococcus lentus, S. sciuri, Bacillus Lantus, Alloiococcus otitis, Aerococcus viridans, Aeromonas salmonicid, Gemella spp, Leuconostoc spp.
Following products are involved in this voluntary recall:
|Product||Package Size||UPC Codes|
|Vagifresh Ball||3 tablets individual pack/packed with Female One||689076499156|
|Vagifresh Gel||2 fl.oz. tube individual pack/Packed with Female One||689076499057|
All lots of the listed products are affected by this recall.
These products were sold via herbal stores, beauty shops, drug stores, internet and mail order.
Consumers in possession of products should also return any unused products to their immediate supplier for a direct refund.
Customers with questions can call USA Far Ocean Group, Inc. at 626-560-2435 Monday through Sunday between 9 a.m. and 5 p.m. (PST) for further instructions or information with respect to the return and refund process.