October 2015
As your facility prepares for Baby-Friendly, part of your job will include one-on-one parent education regarding artificial infant milks (AIM). With that in mind, did you know this:
"On September 22, 2010, Abbott issued a voluntary recall of certain Similac powdered infant formula after identifying a common warehouse beetle (both larvae and adults) in the finished product at their Sturgis, Michigan plant. The company immediately put all product manufactured at the Michigan plant on hold and ceased manufacturing at that location. FDA has advised against consumption of the recalled product and urged consumers to follow the manufacturer's instructions for reporting and returning the formula."
Or that in 2012, the FDA in the United States issued a recall for these products:
Gerber Good Start Gentle Powdered Infant Formula: Recall - Off-Odor
ISSUE: Gerber notified the public that it recalled one lot of Gerber Good Start Gentle Powdered Infant Formula, 23.2 ounce plastic package, because the affected product might have an off-odor noticeable to some consumers. In some cases, spit-up and other gastrointestinal complaints have been reported. The recall applies to batch GXP1684, expiration date of March 5, 2013.
RECOMMENDATION: Consumers who have the product with the batch code and expiration date above should contact the Gerber Parents Resource Center at 1-800-487-7763 for replacement. Gerber is working with retailers to retrieve any remaining product from this batch.
Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:
Complete and submit the report Online: www.fda.gov/MedWatch/report.htm
Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
How can you sign up for regular announcements of recalls on AIM? Go here http://www.fda.gov/Safety/Recalls/ to do so. For those of you who are outside of the US, is there a similar agency in your country who provides this information? Please share that information here for the benefit of Step2Education instructors as well as all the students who receive this message.Does your facility keep a log of what patient receives which AIM as well as a way to contact them (after discharge) if recalls such as these occur and affect them? Where does the liability for your facility end? Just some things to think about and perhaps discuss with your Legal/Ethics departments.
Kathy
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Last Updated: September 2018