Delhaize America (Hannaford Bros) Recalls

FDAMay 4, 2013ME, MA, NH +2 more• Delhaize America (Hannaford Bros)

California Pizza Kitchen Crispy Thin Crust (Nestle) – Plastic Contamination (2013)

Plastic contamination. Four pizzas with specific production codes, are being recalled because they may contain fragments of clear plastic

FDAMay 2, 2013Nationwide• Nestle USA, Inc - Northbrook Pizza Head Office

DiGiorno Pizzeria White Pizza (Nestle) – Plastic Contamination (2013)

Plastic contamination. Four pizzas with specific production codes, are being recalled because they may contain fragments of clear plastic

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Class IIModerate

FDAMay 2, 2013Nationwide• Nestle USA, Inc - Northbrook Pizza Head Office

CLENZIderm (Medicis) – mislabeled product (2013)

cGMP Deviations; during the production process, CLENZIderm M.D. Daily Foam Cleanser was filled into some bottles labeled as CLENZIderm M.D. Pore Therapy

FDAMay 1, 2013Nationwide• Medicis Pharmaceutical Corp

XYMOGEN EP Dietary Supplement (XYMOGEN) – Undeclared Allergens (2013)

Undeclared Soy

Undeclared Soy and Milk on the label.

FDAMay 1, 2013AL, AK, AZ +39 more• Atlantic Pro Nutrients, Inc. dba XYMOGEN

Vicerex Sexual Enhancer (American Lifestyle) – Undeclared Ingredients (2013)

Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared tadalafil and the Black Ant product contains undeclared sildenafil. Tadalafil and sildenafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the Vicerex and the Black Ant products unapproved new drugs.

FDAApr 30, 2013Nationwide• American Lifestyle.Com

Black Ant Supplement (American Lifestyle) – Undeclared Ingredients (2013)

FDAApr 30, 2013Nationwide• American Lifestyle.Com

Nature's Earthly Choice Organic Quinoa (Global) – sand contamination (2013)

Nature's Earthly Choice Organic Quinoa may contain sand and grit.

Class IIILow

FDAApr 26, 2013MA, NY• Global Juices & Fruits LLC

Amoxicillin Oral Suspension (Teva) – Powder Discoloration (2013)

Discoloration: This recall is being carried out due to a yellow to brown discolored Amoxicillin powder on the inner foil seal of the bottles.

Class IIILow

FDAApr 26, 2013Nationwide• Teva Pharmaceuticals USA, Inc.

Maple View Farm Cookies & Cream Ice Cream (Maple View) – undeclared allergens (2013)

Undeclared allergens: Wheat and Soy (soybean oil).

FDAApr 25, 2013NC• Maple View Ice Cream

Maple View Farm Cookie Dough Ice Cream (Maple View) – undeclared allergens (2013)

Undeclared allergens: Wheat and Soy (soy lecithin).

FDAApr 25, 2013NC• Maple View Ice Cream

Maple View Farm Carolina Crunch Ice Cream (Maple View) – undeclared allergens (2013)

Undeclared allergens: Peanuts, Almond and Soy (soy lecithin and soybean oil).

FDAApr 25, 2013NC• Maple View Ice Cream

9100 Power Awning (Dometic) – Equipment Issue (2013)

Dometic is recalling certain WeatherPro motor powered awning models 805, 815, 825, 835, 845, 885, 855, and 905: 9100 Power awning models 910, 912, 913, 914, 915, 916, 917, and 91; and certain awning motor service kits with part numbers starting with 3307923 and 3310423. The serial number range for the WeatherPro and 9100 motor powered awnings is 306XXXXX thru 314XXXXX. These motor powered awnings were either sold in the aftermarket as replacement equipment or installed as original equipment on various recreation vehicles and horse trailers. The awning motor service kits were sold in the aftermarket as service parts for product already installed on recreation vehicles or horse trailers and do not carry an individual serial number. The awning motor service kit must be located by the part number shown above. The motor powered awnings and awning motor service kits were manufactured between February 13, 2013 and April 9, 2013. If the awning or service part installation sequence is not completely followed, the awning motor may unknowingly become damaged.

NHTSAApr 22, 2013Nationwide• DOMETIC

Ropinirole Tablets (Mylan) – Incorrect Labeling (2013)

Labeling: Label Error on Declared Strength- Unopened bottles of Ropinirole USP 3 mg tablets was found to be incorrectly labeled as Ropinirole USP 4 mg tablets..

FDAApr 22, 2013Nationwide• Mylan Pharmaceuticals Inc.

Amlodipine Besylate Tablets (Walmart) – Label Strength Error (2013)

Labeling: Label Error on Declared Strength-The recalled product has a misprint on the Amoldipine 10 mg label, 5 mg is listed in the USP description. Tablet strength is 10 mg.

FDAApr 22, 2013Nationwide• Legacy Pharmaceutical Packaging LLC

Glimepiride Tablets (Qualitest) – Oversized Tablet (2013)

Failed Tablet/Capsule Specifications: One oversized tablet was found in a sealed 100 count bottle of Glimepiride at the retail level.

FDAApr 19, 2013Nationwide• Qualitest Pharmaceuticals

Mini Boden Chunky Cord Dungarees (J.P. Boden) – Choking Risk (2013)

Choking Hazard

The recalled overall corduroy dungaree pants were sold in light brown and red in sizes 0-24 months and 2Y through 4Y. There are two snaps on each side of the overalls, side pockets and a center pocket with a sewn-in black and white tab label. There is a label on the back of the waist of the dungarees with item number 72092. The label inside the back strap of the dungarees reads "Baby Boden" and the buttons read "Mini Boden." Pants shipped directly to consumers came in a bag labeled "Mini Boden."

CPSCApr 18, 2013Nationwide• J.P. Boden Services Inc., of Pittston, Pa.

Fried Onion Powder (Pacific Pure Aid) – Gluten Mislabeling (2013)

The product contained gluten and is sold as gluten free.

FDAApr 17, 2013CA, IL, KY +2 more• Pacific Pure Aid

NORepinephrine IV Sodium Chloride (Unique Pharmaceutical) – mold contamination (2013)

Lack of Assurance of Sterility: A mold like substance was discovered on the surface of an unopened bag of Sodium Chloride 0.9% while prepping the bag for production.

FDAApr 17, 2013PA, TN, TX• Unique Pharmaceutical, Ltd

Roasted Red Bell Pepper Powder (Pacific Pure Aid) – Gluten Mislabeling (2013)

The product contained gluten and is sold as gluten free.