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Category archives for: Recalls

Nationwide Recall of Joyful Slim Herb Supplement

FDA lab analysis of this herb supplement was found to contain the undeclared drug, desmethyl sibutramine, an FDA-approved drug used as an appetite suppressant for weight loss. Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery [...]

PG Voluntarily Recall Scope Mouthwash Bottles

The Procter & Gamble Company (P&G) (NYSE:PG) is voluntarily recalling a small percentage of 1-liter bottles of Scope Original Mint and Scope Peppermint mouthwash with malfunctioning child-resistant caps in the United States and Canada. The company said it is taking this precautionary step after finding that the child-resistant cap does not work in a small [...]

P&G Voluntarily Recalls 4 Hour Decongestant Nasal Spray

The Procter & Gamble Company (NYSE:PG) announced today it is voluntarily recalling its 4-Hour Decongestant Nasal Spray. The product was distributed nationwide in the United States. The company said it is taking this voluntary precautionary step after finding that the product formulation may not meet the expiration dates on the package. This recall is not [...]

Four Product Lots of Recalls Benadryl® Allergy Ultratab™ Tablets

McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling five product lots as an addition to the list of products included in the company’s January 15th, 2010 product recall. The additional lots involved are four product lots of BENADRYL® ALLERGY ULTRATAB™ TABLETS, 100 count, sold in the U.S.; and one product lot of EXTRA STRENGTH [...]

Pfizer Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility

Pfizer Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility Media Contact: Rick Chambers, O: (269) 833-6387 M: (269) 760-0770 Investors Contact: Suzanne Harnett O:(212) 733-8009 M:(646) 256-9250 FOR IMMEDIATE RELEASE – June 03, 2010 – NEW YORK, NY – [...]

West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags Due To Possible Health Risk

West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags Due To Possible Health Risk Contact: DeVaughn Edwards/Sr. Director of Quality Assurance and Compliance. Tel: 732-542-1191 ext. 2723 FOR IMMEDIATE RELEASE – June 03, 2010 – West-Ward Pharmaceuticals Inc., of Eatontown, NJ, is voluntarily recalling all lots of Claris LifeSciences Inc. manufactured [...]

Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Ondansetron in 5% Dextrose Injection, 32 mg/50 mL Manufactured by Claris Lifesciences

Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Ondansetron in 5% Dextrose Injection, 32 mg/50 mL Manufactured by Claris Lifesciences Contact: Aline Schimmel 312-646-6295 FOR IMMEDIATE RELEASE – SCHAUMBURG, IL – June 2, 2010 – Sagent Pharmaceuticals, Inc. today announced the voluntary nationwide recall of all lots of ondansetron injection in 5% [...]

Claris Lifesciences initiates a nationwide voluntary recall of all lots of Ciprofloxacin Inj. USP 200 mg / 100 mL, Ciprofloxacin Inj. USP 400 mg / 200 mL, Metronidazole Inj. USP 500 mg/100 ml and Ondansetron Inj., 32 mg / 50 mL.

Claris Lifesciences initiates a nationwide voluntary recall of all lots of Ciprofloxacin Inj. USP 200 mg / 100 mL, Ciprofloxacin Inj. USP 400 mg / 200 mL, Metronidazole Inj. USP 500 mg/100 ml and Ondansetron Inj., 32 mg / 50 mL. FOR IMMEDIATE RELEASE – June 1, 2010 – Claris Lifesciences today announces the voluntary [...]

Recall: John Frieda Collection Sheer Blonde Lustrous Touch Strengthening Conditioner

PRODUCT: John Frieda Collection Sheer Blonde Lustrous Touch Strengthening Conditioner with Satin Finishers. CODE: Unit: Y321CE27 RECALLING FIRM/MANUFACTURER: Recalling Firm: KAO Brands Co., Cincinnati, OH, Manufacturer: Tri Tech Laboratories, Inc., Lynchburg, VA. REASON Product is contaminated with the microorganism, Burkholderia cepacia. VOLUME OF PRODUCT IN COMMERCE: 5,346 bottles DISTRIBUTION: Nationwide via recalls.org.

Recall: Family Dollar brand Baby Hair & Body Wash

PRODUCT: Family Dollar brand Baby Hair & Body Wash, 15 oz, SKU: 912028, UPC#-400910167679. CODE: None RECALLING FIRM/MANUFACTURER: Recalling Firm: Family Dollar Services, Inc., Charlotte, NC, Manufacturer: RNA Corp., Blue Island, IL. REASON: Incorrect directions for use; Directions for Use include instructions to apply and leave on as a moisturizer. VOLUME OF PRODUCT IN COMMERCE: [...]

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