ISSUE:
Nutek Disposables, Inc. initiated a nationwide voluntary product recall
at the retail level of all lots of baby wipes that it manufactured
under the brand names Cuties, Diapers.com, Femtex, Fred's, Kidgets,
Member's Mark, Simply Right, Sunny Smiles, Tender Touch, and Well
Beginnings, because some packages may contain bacteria. These wipes were
distributed by Nutek prior to October 21, 2014 to the following retail
stores: Walgreens, Sam's Club, Family Dollar, Fred's, and Diapers.com.
After
receiving a small number of complaints of odor and discoloration, Nutek
conducted microbial testing that showed the presence of the bacteria
Burkholderia cepacia (B. cepacia), in some of these products. B. cepacia poses
little medical risk to healthy people. However, people who have certain
health problems like weakened immune systems or chronic lung diseases,
particularly cystic fibrosis, may be more susceptible to infections with
B. cepacia.
As
of October 3, 2014, the date of the original withdrawal, the company
had received only one report of irritation. Numerous reports of
complaints have since been received by the company that include rash,
irritation, infections, fever, gastro-intestinal issues, and respiratory
issues, though these reports have not been confirmed to be related to
the use of these products.
BACKGROUND:
The company has not identified the cause of the problem, but is
continuing to investigate. In the interim, Nutek has stopped shipping
baby wipes manufactured at the facility.
RECOMMENDATION:
Consumers who have purchased this product can return it to the place of
purchase for a full refund. Consumers with questions may contact the
company at 1-855-646-4351, Monday through Friday, 10 AM – 4 PM EDT.
If you believe you have a weakened immune system or chronic lung
disease and you have used one of the affected wipe products, you should
call your doctor promptly for medical advice.
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:
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