Saturday, August 30, 2014

Kraft Recalls Regular Kraft American Singles Pasteurized Prepared Cheese

Kraft Foods Group Voluntarily Recalls Select Varieties of Regular Kraft American Singles Pasteurized Prepared Cheese Product Due to Ingredient Supplier's Out-of-Standard Storage Temperatures


Kraft Foods Group is voluntarily recalling 7,691 cases of select varieties of regular Kraft American Singles Pasteurized Prepared Cheese Product. A supplier did not store an ingredient used in this product in accordance with Kraft’s temperature standards. While unlikely, this could create conditions that could lead to premature spoilage and/or food borne illness; therefore, the company is issuing the recall as a precaution. Kraft has had no consumer illness complaints for this product associated with this recall. The affected product is limited to four varieties with “Best When Used By” dates of February 20, 2015, and February 21, 2015.
The affected product was shipped to customers across the United States. It was not distributed outside of the United States.
The following varieties are being recalled: 
ProductSize
Name of Product
Units/Case
Best When Used By Code Dates
Package Code
Case Code
12 oz.12 oz Kraft American Singles (16 slices)4820 FEB 2015 and 21 FEB 20150 21000 60464 700 21000 60464 00
16 oz.16 oz Kraft American Singles (24 slices) (36 count case)3620 FEB 20150 21000 61526 100 21000 61450 00
16 oz.16 oz Kraft American Singles (24 slices) (12 count case)1220 FEB 20150 21000 61526 100 21000 61526 00
64 oz.64 oz (4 lb) Kraft American Singles (4x24 slice)820 FEB 20150 21000 63360 900 21000 62559 00
Consumers can find the “Best When Used By” dates on the bottom of the product package. No other Kraft Singles products are impacted by this recall.
The affected product was produced at Kraft’s Springfield, MO manufacturing facility.
Consumers who purchased any of these products should not eat them. They should return them to the store where purchased for an exchange or full refund. Consumers also can contact Kraft Foods Consumer Relations at 1-800-396-5512. 


Solace International, Recall of Dermatend Original and Dermatend Ultra Due to Safety Concerns

Solace International, Inc. Issues Voluntary Nationwide Recall of Dermatend Original and Dermatend Ultra Due to Safety Concerns


Solace International, Inc. is voluntarily recalling all lots of Dermatend Original and Dermatend Ultra, in all sizes and dosage form, to the distributor/wholesaler level. A mole should be removed under the supervision of a dermatologist. Dermatend is not FDA approved, thus has not been shown to be safe and effective for the uses suggested in the labeling. Using these Dermatend products instead of seeking medical attention could result in delayed diagnosis of conditions such as cancer.
Currently, the Dermatend Original and Dermatend Ultra products are used to remove moles, warts and skin tags. Dermatend Original and Dermatend Ultra are packaged in a flexible plastic tubes labeled with the product name in blue letters. All units and lots are affected by the recall.
Solace International, Inc. is notifying its distributors/wholesalers by certified letter and is arranging for the return of all recalled products. Distributors/wholesalers that have Dermatend Original and Dermatend Ultra product, which is being recalled, should return all units and cases to Solace International, Inc. Consumers who purchased Dermatend Original and Dermatend Ultra to remove moles and warts should immediately discontinue use and consult their physician.
Consumers with questions regarding this recall can contact Solace International, Inc. at 775-323-1413 orinfo@dermatend.com, Monday through Friday from 8:00 a.m. to 5:00 p.m. PST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Regeneca Worldwide, Expands Recall of Regeneslim Appetite Control Capsules

Regeneca Worldwide, a Division of Vivaceuticals, Inc Expands the Voluntarily Recall of Regeneslim Appetite Control Capsules Due to the Presence of DMAA that May Pose Possible Health Risk


Regeneca Worldwide a division of VivaCeuticals, Inc. Las Vegas, NV is expanding the voluntary nationwide recall of its RegeneSlim appetite control dietary supplement to include lot #823230415, lot #EX0616r 15813, Lot # EX0616R15814 and Lot #11414re5516 because FDA analysis confirmed the presence of DMAA. DMAA is also known as 1,3-dimethylamylamine, methylhexanamine, or geranium extract. DMAA is commonly used as a stimulant, pre-workout, and weight loss ingredient in dietary supplement products. The Food and Drug Administration (FDA) has warned that DMAA is potentially dangerous to health as it can narrow blood vessels and arteries, which can cause a rise in blood pressure or other cardiovascular problems such as shortness of breath, arrhythmias, tightening in the chest, and heart attack. RegeneSlim is purchased by and distributed through a direct sales force within the United States and Puerto Rico, and through online sales, for both personal consumption and retail sales.
RegeneSlim is packaged in approximately 3 1/2” by 3” green and white sachets that contain 2 capsules, with the name RegeneSlim displayed prominently on the front of the sachet.
There have been no illnesses reported to date.
This voluntary recall was the result of FDA analysis confirming the presence of DMAA in RegeneSlim and our company's sampling. The company continues their investigation as to what caused the problem.
Consumers who have purchased RegeneSlim with the above-mentioned lot numbers are advised to immediately stop using the product and are urged to return it to the place of purchase for a full exchange. Consumers with questions may contact the company at 1-949-281-2600 between the hours of 9 a.m. and 6 p.m. PDT. Consumers should contact their physician or healthcare provider if they experience any problems that may be related to taking or using RegeneSlim.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
Complete and submit the report Online: www.fda.gov/medwatch/report.htm disclaimer icon
Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm disclaimer icon or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

4C Foods Corp. Voluntarily Recalls 4C Grated Cheese Homestyle Parmesan Because of Salmonella Contamination

4C Foods Corp. is recalling its 6-oz. glass jars of "4C Grated Cheese HomeStyle Parmesan", UPC 0-41387-32790-8 with code dates BEST BY JUL 21 2016 and JUL 22 2016 due to possible contamination with Salmonella. This recall does not impact any other 4C cheese products.
Salmonella is an organism that can cause serious and sometimes fatal infections in young children, elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses.
No illnesses have been reported to date in connection with this problem.
On July 24, 2014, Product was distributed to: IA, IL, MI, MN, ND, NE, SD, and WI through retail stores.
Item is packed as 12 glass jars per case, code dates BEST BY JUL 21 2016 and JUL 22 2016 can be located on jar back side toward bottom portion.
The potential risk was brought to 4C's attention by FDA during routine testing. This recall affects 308 cases that were shipped of the affected date codes.
Consumers do not need to return the product to the store where it was purchased. Instead, consumers are urged to dispose of the recalled product and its container. Please contact 4C Foods at 1-718-272-7800 ext. 176, Monday – Friday, 9:30 AM to 4:30 PM (Eastern Time), for a replacement or full refund and for general inquires.