Tuesday, August 4, 2015
1012 C Street  •  Floresville, TX 78114  •  Phone: 830-216-4519  •  Fax: 830-393-3219  • 

WCN Site Search


Lost & Found

Lost/dognapped: Black Lab/Pyrenees male puppy, about 30 pounds, vaccination tag on collar, last seen on Wood Valley Dr., Wood Valley Acres, Adkins, Sat., July 18 around noon. 210-827-9533.

VideoLost: Female longhair Chihuahua that had been trimmed, near 3rd and Hwy. 97, Floresville, miss her very much. Call Jeri, 409-781-3191.
Found: Horse by F.M. 2579 and C.R. 126, Floresville. Call 818-416-3372 to describe.
More Lost & Found ads ›

Help Wanted

The Floresville Independent School District is accepting applications for: Licensed Plumber, Monday-Friday from 7:30-4:30. Applications may be submitted online at www.fisd.us. FISD Personnel Office is located at 1200 5th St., Floresville, Texas, 830-393-5300, (Office hours: 8:00–4:30). Applications will be accepted until all positions are filled. An Equal Opportunity Employer. 
Optometric assistant needed for Hill Country Vision Center, no experience necessary, must be a people person, quick learner, multi-tasker, good with computers and time management. Bring resume to 495 10th St., Ste. 105, Floresville, Mon.-Fri. from 8-5. 830-393-7744.
More Help Wanted ads ›

Featured Videos





Video Vault ›
WCN essential oilsWCN Citizens Forum 5/28/15WCN printing

Breaking News


Ritedose recalls mislabeled Albuterol




E-Mail this Story to a Friend
Print this Story
U.S. Food and Drug Administration
January 3, 2011, 4:36pm
1,895 views | Post a comment

The Ritedose Corporation is conducting a voluntary recall of 0.083% Albuterol Sulfate Inhalation Solution, 3 mL (in 25, 30, and 60 unit dose vials). This product is a prescription inhalation solution, administered via nebulization, for the treatment and maintenance of acute asthma exacerbations and exercise induced asthma in children and adults. This product is being recalled because the 2.5 mg/3 mL single use vials are embossed with the wrong concentration of 0.5 mg/ 3 mL and therefore, represents a potential significant health hazard. The following lot numbers manufactured by The Ritedose Corporation under NDC: 0591-3797-83, 0591-3797-30, and 0591-3797-60 are included in the recall: 0N81, 0N82, 0N83, 0N84, 0NE7, 0NE8, 0NE9, 0NF0, 0P12, 0P13, 0P46, 0P47, 0PF0, and 0S15. No other Albuterol formulations or products are included in this recall.

The product is packaged as a single use unit dose vials in a protective foil overwrap packaged in a shelf carton. Only the unit dose vials are incorrectly embossed as containing 0.5 mg/3 mL. The correct concentration of 2.5 mg/3 mL is labeled on the primary foil overwrap pouches and shelf cartons. This product was distributed nationwide and Puerto Rico.

Administration of this defective product could result in a range of potential health effects that spans from temporary and medically reversible to life threatening and death. There is significant concern that health professionals who read the incorrect embossed concentration may upwardly adjust the volume of product used resulting in an administered amount that is 5 times the recommended dose. In the hospital setting, the vials are often not accompanied by the rest of the packaging, making it more likely that such a dosing error could occur. Significant overdosing of a patient could lead to signs and symptoms of albuterol toxicity, which includes tremors, dizziness, nervousness, headache, seizures, angina, high blood pressure, low potassium levels, and rapid heart rates up to 200 beats/minute.

The Ritedose Corporation is working cooperatively with the U.S. FDA to implement a nationwide recall as quickly and efficiently as possible.

Consumers should immediately return the affected product to the place it was obtained (i.e. doctor’s office, pharmacy, etc.). Wholesalers and retailers should return the product to the following address:

Total Product Destruction
Attn: RECALL
8025 Howard Street
Spartanburg, SC 29303

For more information concerning this recall contact The Ritedose Corporation directly at phone: 803-935-3995 Monday through Friday 8am to 5 pm EST or by e-mail: recall@ritedose.com.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program online, or regular mail or by fax.
 

Your Opinions and Comments


Be the first to comment on this story!


You must be logged in to post a comment.




Not a subscriber?
Subscriber, but no password?
Forgot password?

Breaking News Archives


Malcolm's Custom Welding
Connally Memorial MC breaking news banner
Southern Electric
auto chooserVoncille Bielefeld homeTriple R DC ExpertsDrama KidsHeavenly Touch homeAllstate & McBride Realty

  Copyright © 2007-2015 Wilson County News. All rights reserved. Web development by Drewa Designs.