Cubist Pharmaceuticals Issues Voluntary Nationwide Recall of Four Lots of Cubicin (Daptomycin for Injection) 500mg in 10ml Single Use Vials Due to Presence of Particulate Matter

Lexington, Mass. – Cubist Pharmaceuticals, Inc. (NASDAQ: CBST) today announced it is voluntarily recalling four lots of CUBICIN® (daptomycin for injection) to the user level due to the presence of particulate matter found in a number of vials from these lots. No adverse events have been reported to date in association with a product complaint of vials containing glass particulates.

Hardmenstore.com Issues Voluntary Nationwide Recall of 72HP, Evil Root and Pro Power Max Due to Undeclared Sildenafil

Upon request of the FDA, Hardmenstore.com is voluntarily recalling 1000 lots of 72HP, Evil Root and Pro Power Max at the consumer level. According to representatives of the FDA, 72HP, Evil Root and Pro Power Max have reportedly been found to contain amounts of the PDE-5 Inhibitor, sildenafil, which is the active ingredient in an FDA-approved drug for erectile dysfunction (ED).

Wellness Pharmacy, Inc. Issues Nationwide Voluntary Recall of Certain Sterile Products due to Laboratory Results Indicating Microbial Contamination

This recall was initiated after Wellness Pharmacy was notified that in a recent inspection of Front Range Labs, FDA investigators observed methods used by Front Range Labs to assess sterility and other qualities (e.g., strength and stability) may have resulted in Wellness Pharmacy receiving inaccurate sterility test results on these lots.

JCB Laboratories Issues Voluntary Recall of Six Drug Product Lots Due to Concerns of Sterility Assurance at Testing Vendor

WICHITA, Kan. – JCB Laboratories (JCB) is issuing a recall of six lots of sterile drug products to the user level due to concerns of sterility assurance following a recent inspection by the U.S. Food and Drug Administration of Front Range Laboratories of Loveland, Colo., one of the contract testing labs used by JCB. The following compounded products are subject to the recall:

Park Pharmacy & Compounding Center is Issuing a Voluntary Recall of Two Compounded Sterile Preparations. The Recall is Due to a Lack of Sterility Assurance

Irvine, Ca. Park Pharmacy & Compounding Center is voluntarily recalling two lots of products Methylcobalamin 5mg/ml 30ml Amber Vials Lot #06132013@1 Exp: 12/10/2013 and Multitrace-5 Concentrate 10ml Amber Vials Lot #05212013@20 Exp: 11/17/2013 for injection, to the consumer level. In a recent inspection, FDA investigators observed that methods used by the laboratory to assess sterility may have resulted in pharmacies receiving inaccurate laboratory test results.

Dove Chocolate Discoveries Issues Allergy Alert on Undeclared Nuts in Dark Chocolate Covered Fruit Collection Box

MOUNT ARLINGTON, NJ –DOVE CHOCOLATE DISCOVERIES (DCD) is voluntarily recalling its Dark Chocolate-Covered Fruit Collection boxes marked Item #3265D, lot code #317DAIDS01 because some boxes may contain undeclared nuts. People who have an allergy or severe sensitivity to nuts run the risk of serious or life-threatening allergic reaction if they consume this product.

Product Recall of Kroger’s Break ‘n Bake Chocolate Chip Cookie Dough Due to Peanut Butter Cup Cookie Dough Mispacked Into Chocolate Chip Cookie Dough Packages

Today, ConAgra Foods, in cooperation with the U.S. Food and Drug Administration (FDA), is recalling a limited number of Kroger’s Break ‘N Bake chocolate chip cookie dough packages due to peanut butter cup cookie dough inadvertently mispacked into chocolate chip cookie dough packages. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life- threatening allergic reaction if they consume this product.