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February 7, 2012

North Carolina Firm Recalls Chicken Salad Products Due To Possible Listeria Contamination

Bost Distributing Company doing business as Harold Food Company, a Bear Creek, N.C. establishment, is recalling approximately 1,200 pounds of chicken salad products. The products contain eggs that are the subject of a Food and Drug Administration (FDA) recall due to concerns about contamination with Listeria monocytogenes, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today.

The following products are subject to recall: [View Label]

  • 30-lb. boxes of "Harold Food Co. Grand Strand Deluxe Chicken Salad."

Each box has a "Sell By" date of 2/15/2012 and bears the establishment number "P-20479" inside the USDA mark of inspection. The products were sent to a distributor in South Carolina for further distribution to retail establishments in North Carolina and South Carolina. The chicken salad products may have been repackaged as sandwiches under a brand other than Harold Food Co. and no longer bear the identifying information listed above.

Through a follow-up investigation of the FDA's recall of hard-cooked eggs sold by Michael Foods Egg Products Co., it was determined that Bost Distributing Company had received hard-cooked eggs that may be contaminated with Listeria monocytogenes. The chicken salad products contain the recalled eggs and are the subject of this FSIS recall. FSIS, FDA, and the company have received no reports of illnesses associated with consumption of these products.

FSIS routinely conducts recall effectiveness checks to verify that recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at:
www.fsis.usda.gov/FSIS_Recalls/Open_Federal_Cases/index.asp.

Consumption of food contaminated with Listeria monocytogenes can cause listeriosis, an uncommon but potentially fatal disease. Healthy people rarely contract listeriosis. However, listeriosis can cause high fever, severe headache, neck stiffness and nausea. Listeriosis can also cause miscarriages and stillbirths, as well as serious and sometimes fatal infections in those with weakened immune systems, such as infants, the elderly and persons with HIV infection or undergoing chemotherapy. Individuals concerned about an illness should contact a health care provider.

Consumers and media with questions about the recall should contact Bost Distributing Company's General Manager, Jeff Bennett, at (919) 775-5931.

See the full article »

February 7, 2012

Designs Direct Recalls Rooster-Themed Lamps Sold Exclusively at Fred's Inc. Due to Risks of Shock and Fire

Rooster
The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Living Traditions 21-inch Rooster Lamps

Units: About 2,000

Importer: Designs Direct, of Covington, Ky.

Hazard: The electrical cord can fray near the base of the lamp, posing a fire or shock hazard to consumers.

Incidents/Injuries: None reported.

Description: This recall involves Living Traditions 21-inch rooster-themed lamps. The brown polyresin lamps have an off-white shade and a carved 9-inch rooster affixed to the base. A label on the underside of the base reads "Distributed By Fred's Inc" and "SKU 61589."

Sold exclusively at: Fred's Inc. stores nationwide between October 2011 and November 2011 for about $20.

Manufactured in: China

Remedy: Consumers should immediately stop using the recalled lamp and contact Designs Direct for a refund.

Consumer Contact: For more information, contact Designs Direct toll-free at (888) 770-7062 between 7 a.m. and 6 p.m. CT Monday through Friday or visit the firm's website at www.regcen.com/roosterlamp

See the full article »

February 7, 2012

TOYOTA / RAV4 2011

Vehicle Make / Model:             Model Year:
TOYOTA / RAV4                         2011

Component:
Air bags:side/window

Potential Number of Units Affected:
427

Summary:
Toyota is recalling certain model year 2011 RAV4 vehicles, manufactured from November 24, 2011, through December 19, 2011. In the curtain shield airbags, propellant with the incorrect specification was used for the initiator assembled in the airbag inflator. In this condition, the inflator may not perform properly, causing one or both curtain shield airbags to not deploy.

Consequence:
In the event of a crash, the airbags may not deploy and will not be able to properly protect an occupant, increasing the risk of injuries.

Remedy:
Toyota will notify owners, and dealers will check the vehicle identification number to identify the curtain shield assemblies and replace the assemblies as necessary with new ones free of charge. The safety recall is expected to begin early March 2012. Owners may contact Toyota at 1-800-331-4331.

See the full article »

February 7, 2012

HONDA / ACCORD 2012; HONDA / CROSSTOUR 2012

Vehicle Make / Model:         Model year:      
HONDA / ACCORD               2012
HONDA / CROSSTOUR       2012

Component:
Air bags:side/window

Potential Number of Units Affected:
347

Summary:
Honda is recalling certain model year 2012 Accord and Crosstour vehicles. The driver-side or passenger-side side curtain airbag inflator may not have been manufactured according to correct specifications.

Consequence:
In the event of a crash, the side curtain airbag may fail to deploy, increasing the risk of injury.

Remedy:
Honda will replace the driver’s side or passenger’s side side curtain airbag as needed free of charge. The safety recall is expected to begin on or about February 10, 2012. Owners may contact Honda customer service at 1-800-999-1009.

See the full article »

February 6, 2012

Nest Collective Voluntarily Recalls Select Revolution Foods Jammy Sammy - Strawberry Jam & Peanut Butter Snack Size Sandwich Bars Due to a Labeling Error (Undeclared Peanut on Inner Wrapper)

Nest Collective ™ announced today that it is voluntarily recalling 8150 selling units of its Jammy Sammy™ - Strawberry Jam & Peanut Butter Flavor Snack Size Sandwich Bars due to a mislabeled inner wrapper. The cartons contain the best by date June 28, 2012 and are marked with the following universal product code (UPC) #89676600116 6 located on the bottom of the package. People who have an allergy or severe sensitivity to peanuts (or peanut butter) run the risk of serious or life-threatening allergic reaction if they consume these individual bars.

These cartons are sold online and at retail stores nationwide.

No illnesses have been reported in connection with this product and no other Revolution Foods products are affected.

The recall was undertaken because, while the cartons of this lot of product are correctly labeled, some of the individual bars are incorrectly labeled as Grammy Sammy - Honey Graham and Strawberry Yogurt™, and show the ingredient statement of that product. Both the selling unit and individually wrapped bars include information that the product was produced in a facility that processes peanuts as well as other allergens. The Jammy Sammy™ product contains organic peanut flour and organic peanut extract, but the inner wrappers are mislabeled with the Grammy Sammy information. Consumers who are allergic to peanut products should not use these products. People experiencing any health issue should seek immediate medical attention.

Specific UPC codes for these products are below:

 

BrandProductFlavorPackageBest ByUPC
Revolution Foods Jammy Sammy Strawberry Jam & Peanut Butter 5 count carton 06/28/12 8 96766 00116 6

 

 

 

Images of the 5 count carton can be found at http://products.revfoods.com/products/jammy-sammy.1

Consumers who purchased this product should return it to the store where it was purchased for a full refund or contact Nest Collective at info@nest-collective.com.

The recall is being undertaken with the knowledge of the U.S. Food & Drug Administration. Consumers with any questions are asked to call 1-866-362-1562 between the hours of 8am – 8pm EST Monday – Friday and 8am – 5pm EST Saturday & Sunday, or email: info@nest-collective.com.

See the full article »

February 6, 2012

Healthy People Co. Issues a Voluntary Recall of Specific Lots of the Dietary Supplements Found to Contain Undeclared Drug Ingredients

Supplements
Supplements1
Supplements2
Supplements3
Healthy People Co. announced today that it is conducting a voluntary nationwide recall of the company’s dietary supplements sold under the brand names Healthy People Co. specific to the following Lot Numbers:  

Product NamePackagingLots
Mince Belle Dietary Supplement 30 Capsules HPCMB/10-026, HPCMB/10-027, HPCMB/10-029, HPCMB/10-020, HPCMB/10-021; UPC7503013203305
PERFECT Men Dietary Supplement 30 Capsules HPCPM/002; UPC7503013203190
EVERLAX Dietary Supplement 30 Capsules HPCEX/074, HPCEX/076, HPCEX/072; UPC7503013203046
EVER Slim Dietary Supplement 30 Capsules HPCES-079, HPCES-070, HPCES-071; UPC7503013203053
Herbal Drink Acai-man Mangosteen Dietary Supplement 16.6 fl oz HPJAC/004 : UPC7503013203015
EVER SLIM Shake Mix Dietary Supplement Strawberry 17.6 oz HPESSF/168: UPC7503013203084
EVER SLIM Shake Mix Dietary Supplement Chocolate 17.6 oz HPESSC/061: UPC7503013203077

 

 

 

 

 

 

 

 

 

 

 

 

Healthy People Co. is conducting a voluntary recall because FDA lab analysis has confirmed the presence of Sibutramine and Tadalafil, making these products unapproved new drugs.

Sibutramine is an FDA-approved drug for appetite suppressant for the treatment of obesity, making dietary supplements: Mince Belle, Everlax, Ever Slim, Ever Slim Shake Mix Dietary Supplement Strawberry, and Ever Slim Shake Mix Dietary Supplement Chocolate unapproved drugs. It is a Schedule IV controlled substance and because of the risks associated with its use, it should be taken only under the direct supervision of a qualified health care professional. Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk to patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. Sibutramine has been withdrawn from the U.S. marketplace. The active drug ingredient is not listed on the label for the products listed above.

Tadalafil is an FDA-approved drug for the treatment of male Erectile Dysfunction (ED), making Perfect Men Dietary Supplement and Herbal Drink Acai-man Mangosteen Dietary Supplement unapproved drugs.

FDA advises that this poses a threat to consumers because tadalafil may interact with nitrates found in some prescription drugs such as nitroglycerin and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Healthy People Co. advises any customers in possession of the products listed above with matching the lot numbers to return any unused product for a full refund to the company directly. Customers can call 626-939-4132 M-F 9am-5pm (PST) for instructions on the return and refund process.

See the full article »

February 6, 2012

California Firm Recalls Prepared Sandwiches that Contain Hard-Cooked Eggs Produced By Michael Foods.

Eggsalad2
Tunasalad
GH Foods CA, LLC was notified by their supplier that the eggs supplied to them were from Michael Foods, Inc, who recalled Hard-Cooked eggs due to potential contamination by Listeria monocytogenes.

GH Foods CA, LLC, Sacramento, California, is therefore recalling sandwiches, associated with the affected eggs, due to potential contamination of Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and individuals with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and still births among pregnant women.

The sandwiches affected by the recalled eggs from Michael Foods, Inc., were distributed in the state of California. Products were sold in Walgreens retail stores only.

The product is packaged in a cellophane wrapper and sold under the Delish brand. Products affected include the code dates listed below. Code dates are listed on the Principal Display Panel. 

 Product  UPC Code Enjoy by Date
 DeLish brand Egg Salad on HoneyWheat Sandwich  8.5 oz.  0.49022-51925.1  1/17/12 through 2/5/12
 DeLish brand Tuna Salad on Multigrain Bread Sandwich  8.5 oz  0.49022-51928.2  1/22/12 through 2/5/12

 

 

 

 

There have been no confirmed reports of illness associated with these products.

Consumers who may have the product, including expired product, are urged to discard the product or return it to the store for a refund.

If consumers have additional questions or concerns regarding these sandwiches, please contact Donald Johnson at (888) 449-9386, Monday-Friday 8 am – 5 pm, PST.

See the full article »

February 6, 2012

Greencore, USA – Cincinnati, Recalls Egg Salad Sandwiches with Brand Name Quick Café and Take Away Café because of Possible Health Risk

Greencore, USA is recalling approximately 550 pounds of egg salad sandwiches.   

The sandwiches contain eggs manufactured by Michael Foods Inc that are the subject of a previous recall due to possible contamination with Listeria Monocytogenes.

The firm is recalling the product because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.  Individuals concerned about an illness should contact a health care provider.

The problem was discovered when Greencore, USA – Cincinnati, was notified by one of its suppliers that hard-cooked eggs were possibly contaminated with Listeria monocytogenes and were being recalled by Michael Foods Egg Products Co. The egg salad sandwiches contain the recalled eggs. 

The sandwich products were produced starting  Jan. 18, 2012 and then distributed to retail stores in Ohio, Illinois, Indiana, Kentucky and Tennessee. The company has received no reports of illnesses associated with consumption of these products.

The following products are subject to recall

  • 7.66 oz Take Away Café Egg salad sandwiches with the Sell by date of 1/25/12 though 2/7/12. Barcode UPC : 745466128195
  • 5.68 oz Quick Café Egg salad Wedge with an Enjoy by date of 1/22/12 through 2/4/12. Barcode UPC: 073508830042

The source of the problem is with the manufacturer of the eggs, Michael Foods and not Greencore USA Inc. No other Greencore products or manufacturing facilities are affected.

Greencore USA Inc takes food safety and the protection of its customers and consumers very seriously. It has robust traceability and quality systems and took immediate action on being informed of the potential problem, initiating the recall, tracing and accounting for all potentially affected product and quarantining and destroying remaining inventory.

For further questions regarding this recall, please contact the following Greencore representatives:

Media Inquires: Andrew Hearns – VP, Quality and Development – 978-225-2950 - Greencore USA
Customer Inquiries: Mary Young – Technical Manager - 513-645-1985 – Greencore Cincinnati Monday – Friday, 8:00 am – 5:00 pm EST.

See the full article »

February 6, 2012

New Jersey Firm Recalls Cobb and Spinach Salads Due to Possible Listeria Contamination

F&S Produce Company Inc., a Deerfield, N.J. establishment, is recalling approximately 389 pounds of Cobb and spinach salads. The salads contain eggs that are the subject of a Food and Drug Administration (FDA) recall due to concerns about contamination with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The following products are subject to recall: [View Labels]

  • 10-oz. plastic containers of “Fresh Garden Highway Spinach Salad with Bacon”
  • 10.75-oz plastic containers of “Fresh Garden Highway Cobb Salad”

The products subject to recall have a “Sell By” date through 2/8/2012, and bear the establishment number “Est. 39897” as well as the USDA mark of inspection The products were distributed to a warehouse in Pennsylvania for further distribution to retail locations.

The problem was discovered when F&S Produce Company Inc.was notified by one of its suppliers that hard-cooked eggs (a product inspected by the FDA) had tested positive for Listeria monocytogenes, and are being recalled by Michael Foods Egg Products Co. The salads contain the recalled eggs and are the subject of this FSIS recall. FSIS, FDA, and the company have received no reports of illnesses associated with consumption of these products.

FSIS routinely conducts recall effectiveness checks to verify that recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at:  www.fsis.usda.gov/FSIS_Recalls/Open_Federal_Cases/index.asp.

Consumption of food contaminated with Listeria monocytogenes can cause listeriosis, an uncommon but potentially fatal disease. Healthy people rarely contract listeriosis. However, listeriosis can cause high fever, severe headache, neck stiffness and nausea. Listeriosis can also cause miscarriages and stillbirths, as well as serious and sometimes fatal infections in those with weakened immune systems, such as infants, the elderly and persons with HIV infection or undergoing chemotherapy. Individuals concerned about an illness should contact a health care provider.

Media and Consumers with questions about the recall should contact Douglas Nicoll, Ph.D, Director of Technical Services, at 800-886-3316 ext. 217.

See the full article »

February 3, 2012

Bumbleride Recalls Indie & Indie Twin Strollers Due to Fall Hazard

Stroller1
Stroller
Name of Product:
Bumbleride Indie & Indie Twin Strollers

Units: About 28,000 (an additional 2,700 were sold in Canada)

Importer: Bumbleride Inc., of San Diego, Calif.

Hazard: The front wheel can break at the axle hub, causing the stroller to tip and posing a fall hazard.

Incidents/Injuries: There have been 36 incidents of the front wheel cracking, including two reports of the stroller tipping over resulting in minor injuries.

Description: The recalled Bumbleride Indie strollers are model numbers I-107, I-110 and I-205 with a DOM (Date of Manufacture) from January 2009 through August 2011 sold in multiple colors. The DOM (Date of Manufacture) can be found on a white rectangular sticker affixed to the side of the seat frame. The recalled Bumbleride Indie Twin strollers are model numbers IT-108, IT-111, and IT-305 with a DOM (Date of Manufacture) from January 2009 through August 2011 sold in multiple colors. The DOM (Date of Manufacture) can be found on a white rectangular sticker affixed to the underside of the handle.

Sold at: Buy Buy Baby and other baby product stores nationwide, online at Bumbleride.com, and other online retailers between January 2009 and January 2012 for between $500 and $700.

Remedy: Consumers should immediately stop using the recalled strollers and contact Bumbleride to receive a free front wheel retrofit kit.

Consumer Contact: For additional information, visit the firm’s website at www.support.bumbleride.com or contact Bumbleride at support@bumbleride.com or at (800) 530-3930 between 8 a.m. and 4 p.m. PT Monday through Friday.

See the full article »