Recall

Cilantro recall announced due to possible Salmonella contamination

cilantro recall

Best Syndication News

(Best Syndication News) - The US Food and Drug Administration (FDA) announced a voluntary recall of 88.5 pounds of Satur Farms Cilantro due to a the possibility of the fresh produce being contaminated with Salmonella.

Satur Farms Cilantro distributed their produce to New York City and Long Island, New York. The cilantro was only sent to food service customers in ½ pound And 1 pound bulk packaging. There is a small white sticker with the lot number 6361 printed on it. None of the cilantro was sent to retail stores.

No illnesses were reported to the FDA in association with this cilantro recall. Symptoms of Salmonella infection includes fever, diarrhea, nausea, vomiting and abdominal pain. Sometimes the diarrhea can be bloody. The infection can become serious or deadly for the very young, the elderly, and those with a weak immune system. The more serious illness can cause the infection to spread to the bloodstream which can cause arterial infections, endocarditis and arthritis.

Toyota Recall April 2011 – List some RAV 4 and Highlander vehicles with airbag sensor problem

Toyota Recall April 2011 – List some RAV 4 and Highlander vehicle airbag sensor problem

(Best Syndication News) - Toyota has announced a voluntary safety recall involving some RAV 4 and Highlander and Highland HV vehicles because of sensors that control the airbags could malfunction. The airbag check light will illuminate on the dashboard but the company said that the airbag still would be able to work in an accident. However, if both sensors fail then the side curtain airbag would activate along with the seat belt pretensioner.

This recall involves around 94,000 vehicles that were sold in the United States. Certain 2007 and 2008 RAV4 vehicle and certain 2008 Highlander and Highlander HV vehicles are included in this recall. There are not other vehicle models or years announced in this recall.

TOPOMAX recall announced for two lots of prescription medication

TOPOMAX recall announced for two lots prescription medication

Best Syndication News

(Best Syndication News) - Two lots of TOPAMAX® (topiramate) 100mg dosage with 60 tablets in the bottle have been voluntarily recalled because of an unusual odor said the manufacturer, Ortho-McNeil Neurologics Division of Ortho-McNeil-Janssen Pharmaceuticals, Inc. The smell they believe is related to a trace amount of TBA (2,4,6 tribromoanisole). The TBA could have come from a chemical preservative that is applied to wood such as the pallets that were used during transportation. The company received four consumers that reported the smell, which prompted the voluntary recall.

The recall involves around 57,000 bottles, but they believe there are less than 6,000 bottles that are in the marketplace. The two lots were shipped to US and Puerto Rico locations between October 19, 2010 and December 28, 2010.

Ford Recall – List of F150 Pick up trucks and Lincoln Mark LT vehicles being recalled

Ford Recall – List of F150 Pick up trucks and Lincoln Mark LT vehicles being recalled

Best Syndication News

(Best Syndication News) - Ford has issued a recall for potentially 1,325,000 vehicles that could have a problem with the frontal driver side air bags inflator module. In the worst case scenario the defect could cause the front driver side air bag to deploy which could lead to the driver losing control of there vehicle while driving. The National Highway and Traffic Safety Administration (NHTSA) announced that this is an expanded recall to include more vehicles.

The list of model years and vehicles involved in the April 14, 2011 Ford Recall are:

Certain 2004-2006 Ford F-150 Pick Up Trucks
Certain 2006 Lincoln Mark LT vehicles

Citalopram and Finasteride Recall announced because of label mixup says FDA

Citalopram and Finasteride Recall announced because of label mixup says FDA

Best Syndication News

(Best Syndication News) - The US Food and Drug Administration (FDA) announced a recall for citalopram and finasteride prescription medications because the wrong labels may have been put on these bottles mixing the two of them up. Greenston LLC, a subsidiary of Pfizer, is the manufacturers of these two medications that involved in this recall.

The list of recalled citalopram and finasteride prescription drugs are as follows:

• Citalopram 10 mg Tablets (100-count bottle), lot number FI0510058-A

• Finasteride 5 mg Tablets (90-count bottle), lot number FI0510058-A

Syndicate content
Share/Save/Bookmark

      

Post to Facebook

Important: The material on Best Syndication is for informational purposes only and is not meant to be advice. Authors may have or will receive monetary compensation from the company's product/s mentioned. You should always seek professional advice before making any legal, financial or medical decisions and this website cannot substitute or replace any trained professional consultation.
Use of this site means that you agree to our TERMS OF SERVICE

Advertise On This Site
Copyright © 2006-2015 By Best Syndication All Rights Reserved