Feed: FDA Recalls - AggScore: 45.7

Benzocaine and Babies: Not a Good Mix

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Parents should avoid using benzocaine products to relieve teething pain for children under 2. They are at risk for the disease methemoglobinemia.

OSKRI CORP. ISSUES ALLERGY ALERT on UNDECLARED CASHEWS in “PEACH GRANOLA”

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OSKRI Corp. of Lake Mills, WI is recalling 3.53 ounce bags of “Peach Granola”, because it may contain undeclared cashews. People who have an allergy or severe sensitivity to cashews and/or other nuts run the risk of serious or life-threatening allergic reaction if they consume these products.

Teva’s Adderall 30 mg Tablets: Counterfeit Product – Contains Wrong Active Ingredients

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The counterfeit versions of Adderall should be considered as unsafe, ineffective and potentially harmful.

FDA warns consumers about counterfeit version of Teva’s Adderall

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The U.S. Food and Drug Administration is warning consumers and health care professionals about a counterfeit version of Teva Pharmaceutical Industries’ Adderall 30 milligram tablets that is being purchased on the Internet. Adderall, which is approved to treat attention deficit hyperactivity disorders (ADHD) and narcolepsy, is a prescription drug classified as a controlled substance – a class of drugs for which special controls are required for dispensing by pharmacists.

V Maxx RX: Recall – Undeclared Drug Ingredient

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Undeclared active ingredient may interact with nitrates found in some prescription drugs (such as nitroglycerin) and lower blood pressure to dangerous levels.

The Menz Club, LLC . Issues a voluntary nationwide recall of V-Maxx Rx due to undeclared sulfoaildenafil

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An FDA lab analysis of V Maxx Rx Lot # 101109 distributed by The Menz Club, LLC was found to contain undeclared sulfoaidenafil. Sulfoaidenafil is an analog of sildenafil, an FDA approved prescription drug used to treat Erectile Dysfunction (ED), making V Maxx Rx, an unapproved new drug.

Hocean Inc. Recalls Nitre Power 4oz Plastic Bags Because of Possible Health Risks

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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.

Baxa Corporation Abacus Total Parenteral Nutrition (TPN) Calculation Software: Class I Recall – Potential Dosing Errors

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Problems associated with mix-ups related to salt-based or ion-based ordering of electrolytes.

Industry Reminder: Labeling of Ethoxyquin in Animal Feed

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The FDA Center for Veterinary Medicine (CVM) would like to remind industry about the labeling and safe use requirements for ethoxyquin, an approved food additive used in animal feed.

L.A. Link (Huntington Beach) Corporation Recalls Shiitake-Ya Brand Gourmet Shiitake Slices Because Of Possible Health Risk

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L.A. LINK (HUNTINGTON BEACH) CORPORATION of Cerritos, California is recalling Shiitake-Ya brand Gourmet Shiitake Slices with a “SELL BY date” of 04/16/2013 because the mushrooms may be contaminated with the chemicals carbendazim, fluoranthene, and pyrene. Residues of these chemicals are not approved on dried mushrooms.