Montague Elementary School
475 Route 206, Montague, NJ 07827
Phone: 973.293.7131 Fax: 973.293.3391
475 Route 206, Montague, NJ 07827
Phone: 973.293.7131 Fax: 973.293.3391
Health & Nutrition
McNeil , PPC, Inc. has a voluntary recall of certain lots of the following unexpired products:
Children’s and Infant’s Liquid Motrin
Children’s and Infant’s Liquid Tylenol
Children’s Zertec
Children’s Liquid Benedryl
Go to the website: www.mcneilproductrecall.com and check the products you have at home to see if they are being recalled. The NDC # is located just above the product name on the front label. You can request a refund or a high dollar coupon to replace your unexpired products if they are the one’s being recalled.
Children’s and Infant’s Liquid Motrin
Children’s and Infant’s Liquid Tylenol
Children’s Zertec
Children’s Liquid Benedryl
Go to the website: www.mcneilproductrecall.com and check the products you have at home to see if they are being recalled. The NDC # is located just above the product name on the front label. You can request a refund or a high dollar coupon to replace your unexpired products if they are the one’s being recalled.
Product Recall: PediaCare Children’s Products
PediaCare Children's Products [Blacksmith Brand]: Recall of four products
Blacksmith Brands and FDA notified healthcare professionals and patients about a nationwide recall of all lots of four PediaCare children's products. These products are sold exclusively in the United States and were manufactured by McNeil Consumer Healthcare at McNeil's Fort Washington, PA plant.
The four PediaCare items involved in the recall are:
The four PediaCare items involved in the recall are:
PediaCare Multi-Symptom Cold 4oz. UPC # 3 0045-0556-05 9
PediaCare Long Acting Cough 4oz. UPC# 3 0045-0465-04 7
PediaCare Decongestant 4oz. UPC# 3 0045-0554-04 8
PediaCare Allergy and Cold 4oz. UPC# 3 0045-0552-04 4
PediaCare Long Acting Cough 4oz. UPC# 3 0045-
PediaCare Decongestant 4oz. UPC# 3 0045-
PediaCare Allergy and Cold 4oz. UPC# 3 0045-
Blacksmith Brands initiated the recall as a precautionary step because the products were manufactured at a McNeil plant in which a recent FDA inspection found serious problems in meeting FDA's current good manufacturing practice requirements. The company advises consumers who have purchased these recalled products to discontinue use. Read the complete MedWatch 2010 Safety summary, including a link to the firm press release, at: http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm214036.htm