Recalls in August 2013

American Importing Co (d/b/a Amport Foods) of Minneapolis, Minn., is recalling one lot of Amport Milk Chocolate Raisins because they may contain peanuts, an allergen not listed on the label. 

No adverse reactions or illnesses have been reported to date.

This recall is based on a discovery that a container of Milk Chocolate Peanuts was erroneously labeled as Milk Chocolate Raisins.

This product was distributed to Albertsons, Farm Fresh/Supervalu, Hy-Vee and The Kroger Co. stores in the Mid-Atlantic, Midwest and West.

The affected product is as follows:

• 12-oz Clear Tub (UPC: 0 71725 71190 8) Lot Code: 078X344 Best Buy: 12-19-13

The lot number can be found printed on the bottom of the tub in black ink.

The label for this product also includes a statement "ALLERGY INFORMATION: THIS PRODUCT IS PRODUCED ON EQUIPMENT SHARED WITH PEANUT AND TREE NUT PRODUCTS."

 This recall relates only to a single lot of Amport Milk Chocolate Raisins. No other Amport products are affected.

Consumers who purchased the affected product should return it to the place of purchase for a full refund.

Consumers with questions may contact the company at 855-273-0466. Please mention "Milk Chocolate Raisin Recall".

Wellness Pharmacy is recalling the following medications:

This recall was initiated after the firm was notified that Food and drug Administration (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. FDA has concerns that test results obtained from Front Range Labs may not be reliable.

If there is microbial contamination in medications intended to be sterile, patients are at risk of serious infections which may be life threatening. Wellness Pharmacy has yet to receive any reports of adverse events related to this recall.

Recalled medications were distributed to individual patients and physician offices nationwide. The liquid medications are in either clear or amber sterile vials ranging in size from 1ml to 50ml. They can be identified by the label on each vial, which will have the name of the drug, strength or concentration, lot number, use by date, and vial size.

Wellness Pharmacy is notifying customers by phone and regular mail. Patients and physicians should immediately discontinue use of these lots of medications, and return the recalled unexpired medications to Wellness Pharmacy.

To return medication or request assistance related to this recall, patients and physicians should contact Wellness Pharmacy at 205-879-6551 or 800-227-2627, Monday through Friday, between 9 a.m. and 4 p.m. CDT.  

Wilton Industries of Woodbridge, Ill., is recalling about 717,000 Chefmate 2-quart tea kettles in the U.S and Canada.

Steam can travel up the handle, or water can spill from the spout, posing a burn hazard to the consumer. In addition, the leaking steam can cause the kettle to fail to whistle. If water completely evaporates from the kettle, the aluminum bottom can melt onto the stove and pose a burn hazard.

The firm says it has received five reports of steam traveling up the handle, three reports of hot water spilling from the spout and a report of a hot handle. In addition, four consumers reported the tea kettle base melting onto the stove burner. No injuries have been reported.

This recall involves Chefmate 2-quart tea kettles sold with a black enamel finish and a solid black resin handle. The Chefmate logo is stamped on the bottom of the aluminum tea kettle.

The tea kettles, manufactured in Indonesia and China, were sold exclusively at Target stores nationwide and online at Target.com from January 2006, through May 2013, for about $9.

Consumers should immediately stop using the recalled tea kettles and return them to any Target store, or contact Wilton Industries for a full refund.

Consumers may contact Wilton Industries toll-free at (866) 255-9237 from 8 a.m. to 4:30 p.m. CT Monday through Thursday, and 8 a.m. to 1 p.m. CT Friday.

The Procter & Gamble Company is recalling specific lots of dry pet food that have the potential to be contaminated with Salmonella.

The products were distributed in the U.S. and represent roughly one-tenth of one percent (0.1%) of annual production. No Salmonella-related illnesses have been reported to date.

These products were made during a 10 day window at a single manufacturing site. No other dry dog food, dry cat food, dog or cat canned wet food, biscuits/treats or supplements are affected announcement.

Consumers who purchased a product listed below should stop using the product and discard it and contact P&G toll-free at 800-208-0172 (Monday – Friday, 9:00 AM to 6:00 PM EST).

Recalled products include:

EUKANUBA DRY DOG FOODS

IAMS DRY DOG FOODS

IAMS DRY CAT FOODS

Jaguar Land Rover North America is recalling 1,989 model year 2011-2014 XK convertible vehicles manufactured October 1, 2010, through August 1, 2013.

The switch in the overhead roof console, which also activates the power operated windows when the convertible roof is opening or closing, does not move downward to close the windows. The power windows may be activated inadvertently and pinch or injure an arm or finger.

Jaguar will notify owners, and dealers will replace the overhead roof console, free of charge. The recall is expected to begin by September 27, 2013.

Owners may contact Jaguar at 1-800-452-4827. Jaguar's recall number is J030.

Zero Motorcycles is recalling 268 model year 2011 and 2012 S and DS motorcycles.

The front caliper mounting bolts are susceptible to corrosion which could lead to their cracking and possible fracture. If a front caliper bolt fractures, the caliper may come loose and interfere with the rotation of the front wheel. This could cause the front wheel to stop suddenly, increasing the risk of a crash

Zero Motorcycles will notify owners, and dealers will replace the front caliper bolts. The recall is expected to begin mid-August 2013.

Owners may contact Zero Motorcycles at 1-888-841-8085.

Kawasaki Motors is recalling 11,097 model year 2013 Ninja 300 and 300 ABS motorcycles manufactured July 16, 2012, through April 27, 2013.

Due to an improper setting in the Electronic Control Unit (ECU), the motorcycle may stall under deceleration. A stall under deceleration increases the risk of a crash.

Kawasaki will notify owners, and dealers will replace the ECU. The recall is expected to begin in mid-August 2013.

Owners may contact Kawasaki at 1-866-802-9381.