Pediacare Recall

Pediacare Recall

6/4/10: The FDA announced recently that Blacksmith Brands, Inc., is voluntarily recalling four Pediacare products including:
1. PediaCare Multi-Symptom Cold 4oz. UPC # 3 0045-0556-05 9
2. PediaCare Long Acting Cough 4oz. UPC# 3 0045-0465-04 7
3. PediaCare Decongestant 4oz. UPC# 3 0045-0554-04 8
4. PediaCare Allergy and Cold 4oz. UPC# 3 0045-0552-04 4

Blacksmith said the reason for the recall is that these Pediacare products were made at the McNeil Consumer Healthcare Fort Washington, PA plant that has been temporarily shut down. A recent FDA inspection at that facility found serious problems in meeting the FDA's current good manufacturing practice requirements. The recall was not initiated as a result of any consumer reports of adverse events and no consumer complaints have been received about the safety or purity of the products.

A press release issued by the company states, "While the recall was not initiated as a result of either any consumer reports of adverse events or complaints with respect to the PediaCare products, tiny particles have been found in other non-PediaCare products which were manufactured at the McNeil plant. While the potential for serious medical events is remote, the company advises consumers who have purchased these recalled products to discontinue use. Blacksmith Brands is asking Retail and Wholesale customers to withdraw the four products from their shelves and warehouses and return the product to Blacksmith Brands."

The company urges consumers to discontinue use of the recalled products. For more information, see: FDA Press Release 5-28-10