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Lost & Found

Our beloved Gracie is missing since October, Dachshund/Lab mix, microchipped, about 30 pounds, black with little white. $1000 reward for safe return. Call with any information, 830-393-9999 or 419-250-9099.
Lost: Shadow, black female mixed Lab, last seen by F.M. 1303 and Broken Arrow, Jan. 11, white patch on chest, tail curls when happy, 30 lbs. Call/text 817-705-1116.
Found, black and white female dog-Stockdale area. call to identify. 2102165738
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Help Wanted

HEAD REGISTERED NURSE. Camino Real Community Services (CRCS) is looking for a Texas licensed Registered Nurse with clinical psychiatric nursing and management experience to serve as our Lead RN for a Crisis Residential Facility. Position is in Lytle, Texas with hours that are generally between 8 a.m.–7 p.m., Monday through Friday, but includes some weekend coverage-schedule requires flexibility. Must participate in on-call rotation to ensure the facility remains operational. This position is 75% direct care. Submit resume to Camino Real CS, Attn: HRS, P.O. Box 725, Lytle, TX 78052. Fax 830-772-4304. Visit www.caminorealcs.org for details. EOE.
Maverick Grill is hiring wait staff, dishwashers, kitchen help, and line cooks. Apply in person at 6671 U.S. Hwy. 181 N., Floresville, between 2-5 p.m. Monday-Saturday.
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Breaking News


McNeil recalls several over-the-counter medications




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U.S. Food and Drug Administration
January 18, 2011, 9:57am
1,879 views | Post a comment

In consultation with the U.S. Food and Drug Administration (FDA), McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc. is voluntarily recalling, at the wholesale level, certain lots of TYLENOL® 8 Hour, TYLENOL® Arthritis Pain, and TYLENOL® upper respiratory products, and certain lots of BENADRYL®, SUDAFED PE®, and SINUTAB® products distributed in the United States, the Caribbean, and Brazil. These products were manufactured at the McNeil plant in Fort Washington, PA prior to April 2010, when production at the facility was suspended. The company is initiating the recall as a precautionary measure after an extensive review of past production records found instances where equipment cleaning procedures were insufficient or that cleaning was not adequately documented. It is very unlikely that this impacted the quality of these products.

McNeil Consumer Healthcare is also initiating a voluntary recall of certain product lots of ROLAIDS® Multi-Symptom Berry Tablets distributed in the United States, in order to update the labeling. The company initiated the recall after determining that the product labeling does not include the language “Does not meet USP” as required by regulation.

Both of these recalls are being initiated at the wholesale level. No action is required by consumers or healthcare providers and consumers can continue to use the product. These actions are not being undertaken on the basis of adverse events.

McNeil identified the inadequacies as part of a thorough, proactive product quality and process assessment of all McNeil produced products. As previously announced, McNeil has been implementing a Comprehensive Action Plan at its U.S. manufacturing facilities to improve the quality systems at those sites. This product assessment is a key milestone in the implementation of that plan, and the actions being undertaken as a result of the assessment are part of McNeil’s ongoing commitment to ensure that all its products meet the high quality standards that consumers expect.

Consumers can access full product details and other information about the recall on the www.mcneilproductrecall.com website or by calling our Consumer Care Center at 1-888-222-6036 (available Monday-Friday from 8 a.m. -- 8 p.m. ET and Saturday -- Sunday, 9 a.m. -- 5 p.m. Eastern Time).

Any adverse reactions may also be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

• Online: www.mcneilproductrecall.com

• Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at: www.fda.gov/MedWatch/getforms.htm. Mail to address on the pre-addressed form.

• Fax: 1-800-FDA-0178
 


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