Recall notice from NHTSA's Office of Defects Investigation

You are receiving this message because you have requested to be notified if there is a safety recall regarding Vehicles from NHTSA's Office of Defects Investigation.

Please click on the following NHTSA Campaign ID links to view the recall information.

NHTSA Campaign ID Number :	13V049
Manufacturer :	Spartan ERV
Make / Model Years :	SPARTAN / 2008-2009
Subject :	Hydraulic Cylinders Improperly Heat Treated
NHTSA Campaign ID Number :	13V047
Manufacturer :	Rolls-Royce Motor Cars, Ltd.
Make / Model Years :	ROLLS-ROYCE / 2013
Subject :	Fuel Filler Neck Anti-Misfueling Device Missing
NHTSA Campaign ID Number :	13V046
Manufacturer :	Spartan ERV
Make / Model Years :	SPARTAN / 2005-2011
Subject :	Inclinometer may Allow Platform to Tilt too Low
NHTSA Campaign ID Number :	13V043
Manufacturer :	Chrysler Group LLC
Make / Model Years :	CHRYSLER / 2013 DODGE / 2013
Subject :	Fuel Leakage or Engine Stall
NHTSA Campaign ID Number :	13V042
Manufacturer :	Fontaine Modification
Make / Model Years :	FONTAINE / 2011-2013
Subject :	Steering Cross Shaft Assembly may Detach

Thank you,

Recalls Subscription Team
Office of Defects Investigation (ODI)
National Highway Traffic Safety Administration (NHTSA)
U.S. Department of Transportation (DOT)

---

Please follow one of these links to update your profile or unsubscribe.

To file a vehicle safety-related complaint, please go online to our File a Complaint web page, or call us toll-free at 1-888-327-4236.

To find out more about NHTSA, please go to the Safercar.gov website or call our Vehicle Safety Hotline toll-free at 1-888-327-4236.

Our Privacy Policy can be found at this web page.

If you have questions regarding these e-mails, please go to the NHTSA Contact web page.

This is a system-generated e-mail. Do NOT respond to the sender of this e-mail.

Herbalife Issues Allergy Alert due to Undeclared Milk Allergen in Instant Healthy Meal Nutritional Shake Mix Packets

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

Herbalife Issues Allergy Alert due to Undeclared Milk Allergen in Instant Healthy Meal Nutritional Shake Mix Packets

02/22/2013 10:21 PM EST

Herbalife International of America announced the voluntary recall of certain lots of its niche Instant Healthy Meal Nutritional Shake Mix packets because the label identifies the product as dairy-free, when it may in fact contain trace amounts of milk proteins. Individuals with severe allergies to milk run the risk of serious or life-threatening allergic reaction if they consume products containing milk proteins.

. For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? support@govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420

Voluntary Recall of Dakota Specialty Milling Select Flours and Grain Blends

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

Voluntary Recall of Dakota Specialty Milling Select Flours and Grain Blends

02/22/2013 08:30 PM EST

Dakota Specialty Milling has initiated a voluntary recall of a limited number of its specialty flours and grain blends in cooperation with the Food and Drug Administration due to the possible presence of fragments of thin metal wire from a defective screen on one of its manufacturing lines at a milling facility. This recall was initiated as a precaution to ensure consumer product safety.

. For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? support@govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420

King Arthur Flour Voluntarily Recalls Flour

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

King Arthur Flour Voluntarily Recalls Flour

02/22/2013 06:06 PM EST

February 22, 2013 - Norwich, Vt. – King Arthur Flour has initiated a voluntary recall of a limited number of its bags of flour due to the possible presence of small (7-9 mm) blue polyurethane balls that are used in the sifting process. The balls have a smooth surface and no sharp edges and are made from food grade material.

. For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? support@govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420

Affymax and Takeda Announce a Nationwide Voluntary Recall of All Lots of OMONTYS® (peginesatide) Injection

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

Affymax and Takeda Announce a Nationwide Voluntary Recall of All Lots of OMONTYS® (peginesatide) Injection

02/23/2013 10:30 PM EST

Affymax, Inc. (Nasdaq: AFFY) and Takeda Pharmaceutical Company Limited (Takeda) today have decided to voluntarily recall all lots of OMONTYS® (peginesatide) Injection to the user level as a result of new postmarketing reports regarding serious hypersensitivity reactions, including anaphylaxis, which can be life-threatening or fatal. The companies have been working actively with the U.S. Food and Drug Administration (FDA) which has indicated its agreement with this decision.

. For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? support@govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420

Hy-Vee Issues VoluntaryRecall of Certain Dog Food Products

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

Hy-Vee Issues VoluntaryRecall of Certain Dog Food Products

02/23/2013 09:22 AM EST

Hy-Vee, Inc. today issued a voluntary recall of certain bags of Hy-Vee dog food due to elevated levels of a chemical contaminant commonly found in corn. Routine random tests conducted by the Iowa Department of Agriculture indicated higher-than-normal levels of aflatoxin in some samples of Hy-Vee dog food produced at a Kansas City plant operated by Pro-Pet, LLC.

. For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? support@govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420

Bruce Foods Corporation Expands Recall to Indiana of Food Club Red Enchilada Sauce Because of Possible Health Risk

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

Bruce Foods Corporation Expands Recall to Indiana of Food Club Red Enchilada Sauce Because of Possible Health Risk

02/23/2013 01:22 PM EST

Bruce Foods Corporation of New Iberia, LA is recalling mislabeled cans of 10 oz Food Club Red Enchilada Sauce with code GES 462449, Best Before Date: 12/3/2016 that could contain Green Enchilada Sauce instead of Red Enchilada Sauce. Only the Food Club Green Enchilada contains wheat and soy.

. For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? support@govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420