Babyganics bubble bath recalled due to possible bacterial contamination

Consumers should visit babyganicsbubblebathrecall.com to cheque product status

RACINE, Wis.
,

April 19, 2022

/PRNewswire/ — Babyganics is voluntarily recalling ii lots of xx-ounce bottles of babyganics® 20oz chamomile verbena bubble bath, due to the presence of the bacterium
Pluralibacter gergoviae.

During internal testing related to product shelf life beyond the Babyganics bubble bathroom line, it was discovered that 2 specific lot numbers of this product contained the bacterium. While infants may be more than susceptible than adults,
Pluralibacter gergoviae
does not usually crusade salubrious individuals to get ill. However, information technology may pose a risk of infection to those who are immunocompromised or accept broken or irritated skin, such as diaper rash.

The simply products afflicted are babyganics® 20oz chamomile verbena bubble bathroom UPC eight 13277 01375 four with lot codes
Y314
and
Y315
found at the bottom of the packaging and contained in a white plastic bottle with a light-green plastic lid. The products were sold in the last two months only at select retailers in the U.S. Our testing confirmed that no other Babyganics products contained this bacterium.

Babyganics takes pride in its commitment to vigorous consumer safety standards and providing peace of mind for parents, which is why the decision was made to voluntarily recover these bottles from retailers and to proactively reach out to consumers. Consumers with the afflicted product will be provided a full refund afterward submitting their product and contact information at babyganicsbubblebathrecall.com. This website will also provide instructions to consumers for how to dispose of the product.

Consumers who accept come into contact with the affected production and aren’t feeling well should contact their doctor. The Babyganics wellness and rubber squad is also bachelor 24/7 at 833-359-6304. Additionally, whatever adverse events with the utilise of this production should be reported via the FDA’s MedWatch Program by one of the following methods:

Past telephone at 888.463.6332

By mail:

MedWatch
The FDA Rubber Information and Adverse Event Reporting Plan
US Nutrient and Drug Assistants
Center for Drug Evaluation and Research
5600 Fishers Lane,
Rockville Doctor
20857-0001
On the MedWatch Web site at: http://www.fda.gov/medwatch/

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SOURCE Babyganics