US Recalls

Posted By Jim Vititoe on February 28, 2011

E&J Brandy Announces A Nationwide Recall Of Stainless Steel Flasks Due To Possible Lead Risk

Contact:
John Segale
916-600-1081

FOR IMMEDIATE RELEASE - February 25, 2011 - E&J Brandy announces the following voluntary recall. Consumers should immediately stop using the stainless steel flask sold in E&J® VSOP gift sets in 2006, 2007, 2008, 2009 and 2010 and in E&J® XO gift sets sold in 2006. This voluntary recall pertains only to stainless steel flasks manufactured for E&J Brandy because laboratory results revealed that brandy stored in the flask under certain conditions may show elevated levels of lead. Prolonged exposure to elevated levels of lead may have negative health effects. This recall does not pertain to any bottles of E&J Brandy.

The affected flasks included in the 2006, 2007, 2008, 2009 and 2010 E&J® VSOP gift sets are silver, rectangular in shape and have “E&J VSOP” etched on the front. The affected flasks included in the 2006 E&J® XO gift sets are silver and round in shape with “E&J” etched on the front. These gift sets were sold throughout the United States through a variety of retail stores as recently as this past holiday season. Some flasks in leather cases were also given away as a promotional item in 2007.

Consumers in possession of an affected stainless steel flask should call the consumer recall hotline at 1-866-959-8477 at any time for instructions on how to return the product and receive a full refund. The brandy contained in the gift set is unaffected and may be safely consumed but any brandy or other liquid in the flask should not be consumed.

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

Category: FDA | No Comments »
Tags: lead

Posted By Jim Vititoe on February 28, 2011

Contact:
Raymond Leung
718-963-1010

FOR IMMEDIATE RELEASE - February 17, 2011 - W H & Group LLC., at 287 Vandervoort Ave, Brooklyn, New York 11211 is recalling Dried Fish discovered by New York State Dept. of Agriculture and Markets Food Inspectors during a routine inspection and subsequent analysis of product by food lab personnel confirming that the fish was not eviscerated prior to processing.

This product may be contaminated with Clostridium botulinum spores, which can cause Botulism, a serious and potentially fatal food-borne illness.

The sale of this type of fish is prohibited under New York State Agriculture and Markets regulations because Clostridium botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish has been linked to outbreaks of botulism poisoning. Symptoms of botulism include blurred or double vision, general weakness, poor reflexes, difficulty swallowing and respiratory paralysis.

The recalled Dried Fish comes in an unmarked cardboard box. Each fish is approximately 7-7.5 inches in length. The fish is sold in a bulk form or and may be re-packed into clear unlabeled, uncoded plastic bags. It is a product of China. The product was sold in New York State.

No illnesses have been reported to date in connection with this problem. Consumers who have Dried Fish are advised not to eat it, but should return it to the place of purchase. Consumer with questions may contact the company at 718-963-1010.

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

Category: FDA | 2 Comments »
Tags: Clostridium botulinum spores

Posted By Jim Vititoe on February 28, 2011

Contact:
Carrie Price
209-835-6300

FOR IMMEDIATE RELEASE - February 24, 2011 Tracy, California – Taylor Farms Pacific is voluntarily recalling the follow items with the specific product codes dates in a limited distribution showing Best if Used by from 2/7/11 to 3/7/11 out of an abundance of caution due to a possible health risk from Listeria monocytogenes. No illnesses have been reported in association with the recall.
Listeria monocytogenes is a bacterium that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include fever, muscle aches, gastrointestinal symptoms such as nausea or diarrhea. Most healthy adults and children rarely become seriously ill. The illness primarily impacts pregnant women and adults with weakened immune systems.

This precautionary recall is being conducted to reach retailers as well as consumers. Consumers should check their refrigerators for the above mentioned items with the code date from 2/7 to 3/7. If they have the product, they should not consume it, but rather immediately discard it. Retailers should immediately stop the sale of the affected products and check their inventories and store shelves to confirm that none of the product is mistakenly present or available for purchase by consumers or in warehouse inventories. Taylor Farms customer service representatives are already contacting retailers and are in the process of confirming that the recalled product is not in the stream of commerce. The cases were distributed by Taylor Farms to 6 states, including; CA, AZ, NV, OR, UT, WA. Distribution dates were
from February 7 to February 24.

The precautionary recall notification is being issued due a positive result for Listeria monocytogenes in a random sample collected and analyzed by the Washington Department of Agriculture. Taylor Farms is coordinating closely with regulatory officials. Immediately upon learning about the positive test result, Taylor Farms conducted a traceability assessment and a full review of its food safety documentation, all of which were found to be in compliance.

Retailers and Consumers with questions may call the Taylor Farms Response Center at 209-835-6300 Monday – Friday, 8 a.m. – 5 p.m., Pacific Time.

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

Category: FDA | 1 Comment »
Tags: listeria monocytogenes

Posted By Jim Vititoe on February 28, 2011

NHTSA Campaign ID Number : 11V120
Manufacturer : RICHIE’S AUTO RESTYLING
Make / Model Years : WEBASTO / 9999
Subject : SUNROOF SEPARATION
NHTSA Campaign ID Number : 11V118
Manufacturer : AUTO ACCENTS
Make / Model Years : WEBASTO / 9999
Subject : SUNROOF SEPARATION
NHTSA Campaign ID Number : 11V116
Manufacturer : DUTTON’S UPHOLSTERY
Make / Model Years : WEBASTO / 9999
Subject : SUNROOF SEPARATION
NHTSA Campaign ID Number : 11V115
Manufacturer : TOYOTA MOTOR NORTH AMERICA, INC.
Make / Model Years : LEXUS / 2006-2007
Subject : FLOOR CARPET PAD
NHTSA Campaign ID Number : 11V114
Manufacturer : SUNROOF & RESTYLERS CITY, INC
Make / Model Years : WEBASTO / 9999
Subject : SUNROOF SEPARATION
NHTSA Campaign ID Number : 11V113
Manufacturer : TOYOTA MOTOR NORTH AMERICA, INC.
Make / Model Years : LEXUS / 2008-2011
TOYOTA / 2003-2010
Subject : PEDAL ENTRAPMENT
NHTSA Campaign ID Number : 11V112
Manufacturer : TOYOTA MOTOR NORTH AMERICA, INC.
Make / Model Years : LEXUS / 2004-2007
TOYOTA / 2004-2006
Subject : FLOOR CARPET COVER
NHTSA Campaign ID Number : 11V110
Manufacturer : DAIMLER TRUCKS NORTH AMERICA
Make / Model Years : FREIGHTLINER / 2011
WESTERN STAR / 2011
Subject : ALTERNATOR CABLE ROUTING
NHTSA Campaign ID Number : 11V109
Manufacturer : DAIMLER TRUCKS NORTH AMERICA
Make / Model Years : FREIGHTLINER / 2010-2011
Subject : REAR SUSPENSION SPRING FRACTURE
NHTSA Campaign ID Number : 11V108
Manufacturer : AMERICAN SUZUKI MOTOR CORP.
Make / Model Years : SUZUKI / 2008-2010
Subject : REGULATOR ASSEMBLIES
NHTSA Campaign ID Number : 11V107
Manufacturer : FORD MOTOR COMPANY
Make / Model Years : FORD / 2005-2006
Subject : INADVERTANT DRIVER AIR BAG DEPLOYMENT
NHTSA Campaign ID Number : 11V104
Manufacturer : THINK NORTH AMERICA, INC.
Make / Model Years : THINK / 2011
Subject : TRANSMISSION PARK MECHANISM ADJUSTMENT
NHTSA Campaign ID Number : 11V103
Manufacturer : SHOWHAULER TRUCKS INC.
Make / Model Years : SHOWHAULER / 2003-2006
Subject : REFRIGERATORS/POSSIBLE FIRE/NORCOLD
NHTSA Campaign ID Number : 11V099
Manufacturer : DIAMOND COACH CORPORATION
Make / Model Years : DIAMOND COACH / 2006-2010
Subject : EVAPORATOR ASSEMBLIES/POSSIBLE FIRE
NHTSA Campaign ID Number : 11V092
Manufacturer : POP’S TOP SHOP
Make / Model Years : WEBASTO / 9999
Subject : SUNROOF SEPARATION

Category: National Highway Traffic Safety Administration Office of Defects Investigation (ODI) | 1 Comment »
Tags:

Posted By Jim Vititoe on February 25, 2011

Contact:
(718) 894-5145

FOR IMMEDIATE RELEASE - February 18, 2011 - New York State Acting Agriculture Commissioner Darrel J. Aubertine today alerted consumers to undeclared peanuts in Dry Fruit “Kachori”, packaged and distributed by Maya Overseas Food Inc., located at 48-85 Maspeth Ave in Maspeth, New York. People who have severe sensitivity to peanuts may run the risk of serious or life-threatening reactions if they consume this product.

The recalled Dry Fruit “Kachori” are packaged in a 8.75 ounce, cardboard box. There is no apparent production code on the package. Product distribution includes 13 states (NY, FL, NJ, CT, MA, VA, NH, NC, VT, DE, MD, GA, PA) and Puerto Rico.

Routine sampling by New York State Department of Agriculture and Markets’ food inspectors and subsequent analysis of the product by the New York State Food Laboratory revealed the product contained peanut allergens, which were not declared on the label.

No illnesses have been reported to date to this Department in connection with this product. Consumers who have purchased Dry Fruit “Kachori” may return to place of purchase or discard the product. Consumers with questions about the recalled product may phone the distributor at (718) 894-5145.

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

Category: FDA | No Comments »
Tags: peanut allergens

Posted By Jim Vititoe on February 25, 2011

Contact:
Carol Armenta
(323)319-1503

FOR IMMEDIATE RELEASE - February 17, 2011 - Pacific American Fish Co, Inc. of Vernon, California is recalling SHI306 Shishamo 4L 5PC (23-28G) Wild, Pack 4/20TR, Lots 202885-2 & 201011-3, Master Carton information. Based on FDA Import Alert, this type of processing and size of product has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause food borne illness. Consumers are warned not to use the product even if it does not appear to be spoiled.

Common symptoms of C. botulinum may be difficulty in breathing, weakness of other muscles, abdominal distension and constipation. C. botulinum can also cause the further symptoms if Shishamo was not properly cooked at recommended temperatures and consumed in large quantities. Those people with compromised immune systems, the elderly, and children have a higher risk and could possibly experience general weakness, dizziness, double-vision and trouble speaking or swallowing. People experiencing these problems should seek immediate medical attention.

Product was distributed in California, Kansas, Hawaii, Washington, New York, Texas via retail stores.

Shishamo Roe Capelin in retail packages can be identified as 5 pieces of frozen fish packaged in a styrofoam plate, wrapped in plastic. Label reads Pacific American Fish Co, Roe Capelin, and says Shishamo in Japanese script.

No illnesses have been reported to date, this product recall is prompted by FDA’s Import Alert regarding the salt-cured, uneviscerated fish, larger than 5 inches in length. The Shishamo in question exceeded that size parameter by 1/4″ to 1 1/4 inches and therefore is slightly over the stated regulation.

Should you have any Pacific American Fish Co. Shishamo Roe Capelin, please return to place of purchase for a full refund. Consumers may contact the company at (323) 319-1503, Monday - Friday, 8:00 AM -. 5:00 PM PST for additional information.

Thank you for your attention to this matter.

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

Category: FDA | 1 Comment »
Tags: clostridium botulinum

Posted By Jim Vititoe on February 25, 2011

Contact:
Steve Spatzier
800-257-6174 / 609-654-7901 EXT. 280

FOR IMMEDIATE RELEASE - February 23, 2011 - Haddon House of Medford, New Jersey is recalling Asian Gourmet Cheese Rice Crackers (UPC 076606-710889), because it may contain undeclared milk and food coloring additives used to create the cheese powder listed on the label. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

The Asian Gourmet Cheese Rice Crackers was distributed in the following states and was distributed by Haddon House Food Products to numerous retailers: AL, CT, DE, FL, GA, IL, IN, KY, ME, MD, MA, MI, MS, NH, NJ, NY, NC, OH, PA, RI, SC, TN, VT, VA, Washington, DC, WV, WI.

Specific information on how the product can be identified is as follows. This recall includes all lot numbers. Product is packed in a semi transparent cellophane package red in color with a black and white logo ASIAN Gourmet – Rice Crackers – Cheese. The UPC number of 076606-710889 can be found on the back of the package next to the Nutritional Panel.

As of this date, no illnesses have been reported due to this recall. This recall was initiated when it was discovered the following ingredients had not been included on the products’ ingredient statement: the ingredients of the cheese powder (Cheese Solids, Milk Solids, Salt, Disodium Phosphate, Calcium Chloride, FD & C Yellow 5, FD & C Yellow 6, Silicon Dioxide). The packaging does not declare the milk allergen.

This is a voluntary recall. Anyone possessing this product may return it to their place of purchase for a full refund. Please address any questions or concerns you have pertaining to the recall of Asian Gourmet Cheese Rice Crackers to Steve Spatzier, Haddon House Food Products, Inc., telephone 1-800-257-6174 between the hours of 8 a.m. and 5 p.m. Monday through Friday eastern standard time.

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

Category: FDA | No Comments »
Tags: undeclared milk

Posted By Jim Vititoe on February 25, 2011

Contact:
Steve Cutter
Phone: 510-653-8212
E-mail: natcho86@juno.com

FOR IMMEDIATE RELEASE - February 18, 2011- Oakland, CA – Natural Choice Distribution Company Inc. is recalling certain ready-to-eat sandwiches and wraps because the products’ labels fail to declare food allergens:

• Products that have “cheese” listed as an ingredients do not declare the allergen MILK
• Products that have “whole grain bread” listed as an ingredient do not declare the allergens WHEAT and SOY
• Products that have “expeller pressed canola mayonnaise” listed as an ingredient do not declare the allergen EGG

No illnesses have been reported. People who have allergies to MILK, WHEAT, SOY, OR EGGS run the risk of a serious or life-threatening allergic reaction if they consume these products.

Fare and Square Sandwiches, Superfresh Sandwiches, and Real Wraps Burritos ready to eat sandwiches and wraps are distributed throughout California. The products affected are listed below.

Only products with the following USE BY dates are included:

All Real Wraps burritos
With USE BY dates: 2/20, 2/21, 2/22, 2/23, 2/25, 2/26, 2/27 and 2/28
UPC codes: 614294201038, 614294201052, 61429201090, 614294201076, 614294201120

Superfresh Foods Avocado, Jack and Tomato sandwich and Vegetarian Smoked Turkey sandwich
With USE BY dates: 2/21, 2/22, 2/23 and 2/24
UPC codes: 614294030157, 614294035992

All Fare and Square sandwiches
With USE BY dates: 2/21, 2/22, 2/23 and 2/24
UPC codes: 011059107800, 011059108005, 011059108814, 011059108104, 011059108203

Natural Choice Distribution Company is taking this action to protect consumers who may be unaware that the ingredients contain the aforementioned allergens. The Company is currently putting additional allergen labels on all of the affected products but there is a possibility of some products with undeclared allergen labels still out at retail stores or in consumers’ homes.

Consumers who have purchased these Fare and Square Sandwiches, Superfresh Sandwiches, and Real Wraps Burritos and are sensitive to these allergens are urged to return them to the place of purchase for full refund. Consumers with questions may contact Natural Choice Distribution Company Inc. at 1-510-653-8212 Monday through Friday between 8:00 am and 5:00 pm Pacific Standard Time.

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

Category: FDA | No Comments »
Tags: Undeclared Allergens

Posted By Jim Vititoe on February 25, 2011

Vehicle Make / Model: Model Year(s):
HONDA / FIT 2009-2010
Manufacturer: HONDA (AMERICAN HONDA MOTOR CO.) Mfr’s Report Date: FEB 16, 2011
NHTSA CAMPAIGN ID Number: 11V101000 NHTSA Action Number: N/A
Component: ENGINE AND ENGINE COOLING
Potential Number of Units Affected: 97,201
Summary:
HONDA IS RECALLING CERTAIN MODEL YEAR 2009-2010 HONDA FIT VEHICLES. THERE IS A POTENTIAL FOR ONE OR MORE OF THE FOUR SPRING ASSEMBLIES ON THE ENGINE’S VARIABLE VALVE TIMING AND LIFT ELECTRONIC CONTROL (VTEC) SYSTEM TO FAIL.
Consequence:
A FAILURE OF THE SPRING ASSEMBLIES MAY CAUSE THE VEHICLE TO STALL DURING OPERATION INCREASING THE RISK OF A CRASH.
Remedy:
DEALERS WILL INSPECT AND REPLACE THE SPRING ASSEMBLIES IN THE ENGINE IF NECESSARY FREE OF CHARGE. THE SAFETY RECALL IS EXPECTED TO BEGIN ON OR BEFORE MARCH 7, 2011. OWNERS MAY CONTACT HONDA AT 1-800-999-1009.
Notes:
HONDA’S SAFETY RECALL NO. R66. OWNERS MAY ALSO CONTACT THE NATIONAL HIGHWAY TRAFFIC SAFETY ADMINISTRATION’S VEHICLE SAFETY HOTLINE AT 1-888-327-4236 (TTY 1-800-424-9153), OR GO TO HTTP://WWW.SAFERCAR.GOV .

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

Category: National Highway Traffic Safety Administration Office of Defects Investigation (ODI) | 1 Comment »
Tags: spring assembly failure

Posted By Jim Vititoe on February 25, 2011

Contact:
Hua Shing International Trading Corp
Goa Wen: 212 -219 -1067
Tel: (212) 219 -1067
Fax: (212) 925-0042

FOR IMMEDIATE RELEASE - February 16, 2011 - HUA SHING INTERNATIONAL TRADING CORP AT 50 ELDRIDGE ST-1FL NEW YORK, NEW YORK, 10002 is recalling FROZEN SCDA (fish) discovered by New York State Department of Agriculture and Markets Food Inspectors during a routine inspection and subsequent analysis of product by Food Laboratory personnel confirming that the fish was not properly eviscerated prior to processing.

This product maybe contaminated with Clostridium botulinum spores, which can cause Botulism, a serious and potentially fatal food –borne illness.

The sale of this fish is prohibited under New York State Agriculture and Markets regulations because Clostridium botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish has been linked to outbreaks of botulism poisoning. Symptoms include blurred or double vision, general weakness, poor reflexes, difficulty in swallowing and respiratory paralysis.

The recalled FROZEN SCDA (fish) comes in a 400 gram (14oz.) vacuum packed plastic bag with the code 111 and is a product of China. FROZEN SCDA (fish) was sold in New York City.

No illnesses have been reported to date in connection with this problem. Consumers who have FROZEN SCDA (fish) are advised not to eat it, but should return it to the place of purchase. Consumers with questions may contact the company at 212-219-1067.

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

Category: FDA | No Comments »
Tags: botulism