FDA Warning about Kids Spinbrush

Feb 20 2012

FDA Warning about Kids Spinbrush

FDA Warns Spinbrushes Are Potential Choking Hazard

The FDA recently released a warning about a certain children’s toothbrush. If you have this brush, bring it in and we’ll swap it out with a safer manual brush. Below is the alert released by AAPD (American Academy of Pediatric Dentistry):

recalled brushesThe U.S. Food and Drug Administration (FDA) issued a warning to parents, caregivers, consumers, and dental care professionals about reports of serious injuries and potential hazards associated with the use of all models of the Spinbrush — specifically the Arm & Hammer or Crest Spinbrush. Reports warned that while turned on, the brush head has either “popped off” or broken off in the user’s mouth or near the face, causing cuts to the mouth and gums, chipped or broken teeth, swallowing and choking on the broken pieces, and injuries to the face and eyes.

The manufacturers of the Spinbrush have added a safety warning to the packaging and taken other steps to lessen the risk since the FDA began investigating complaints about the toothbrushes last year, a news release stated.

Advice to Parents, Caregivers and Consumers

Before using the Spinbrush, inspect it for any damage or loose brush bristles. If you find any, do not use the brush. Report it to Church & Dwight, which can be reached toll-free at (800) 352-3384 or (800) 561-0752.

Make sure the brush head is connected tightly to the brush handle, and test the brush outside of your mouth before using. If the connection feels loose or the brush head easily detaches from the handle, do not use the brush. Report it to Church & Dwight.
Use care not to bite down on the brush head while brushing.

To prevent injuries, always supervise children and adults who may need assistance when using the Spinbrush.

Follow the instructions and recommended replacement guidelines included with the Spinbrush.

Report injuries or problems with the Spinbrush to MedWatch- the FDA’s Safety Information and Adverse Event Reporting Program – either online (http://www.fda.gov/MedWatch), by regular mail, by fax or by phone.

Regular Mail: Use postage-paid, pre-addressed FDA form 3500 (http://www.fda.gov/MedWatch)
Fax: (800) FDA-0178
Phone: (800) 332-1088

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