All models of the electric Spinbrush can break into small parts and cause potentially serious problems, according to the FDA that regulates toothbrushes as medical devices intended to help prevent tooth decay.

• Spinbrush Proclean
• Spinbrush ProClean Recharge
• Spinbrush Pro Whitening
• Spinbrush SONIC
• Spinbrush SONIC Recharge
• Spinbrush Swirl
• Spinbrush Classic Clean
• Spinbrush For Kids
• Spinbrush Replacement Heads

“FDA’s concern is that the unexpected release of any part of this battery-powered toothbrush during use poses a risk of injury,” says Steven Silverman, director of the Office of Compliance in FDA’s Center for Devices and Radiological Health. “And the risk is higher in children or adults who may need assistance but are not supervised while using the toothbrush.”

Parents, caregivers, and consumers are urged to routinely check for damaged or loose bristles before turning on the Spinbrush, and to make sure the brush head is connected tightly to the handle.

“It’s important that consumers know how to avoid the risks associated with using the Spinbrush,” says Shumaya Ali, M.P.H., a consumer safety officer at the Food and Drug Administration. “We’ve had reports in which parts of the toothbrush broke off during use and were released into the mouth with great speed, causing broken teeth and presenting a choking hazard.”

Suspect a problem? Call Spinbrush manufacturer Church & Dwight Company, Inc. at 800-352-3384 or 800-561-0752.

File a voluntary report of injuries or problems with the FDA by phone (800-332-1088), fax (800-332-0178), online, or sending a postage-paid, pre-addressed FDA form 3500 via regular mail.

Source: FDA Consumer Health Information

FDA Safety Notice: Please remember to replace your brush head after 3 months of use, or if the brush is damaged, or if parts become loose. Extended usage, loose parts or excessive wear could lead to brush head breakage, generation of small parts and possible choking hazard. Inspect brush for loose parts before use.

Toothbrush Can Chip Teeth and Cause Choking The Saturday Evening Post

For example, on March 16, 2011, the FDA released a Consumer Update advising that the only over-the-counter asthma inhaler sold in the U.S. will no longer be available after December 31 as part of an international agreement to stop the use of substances that damage the environment. Primatene Mist (epinephrine) inhalers, FDA approved for temporary relief of occasional symptoms of mild asthma, are being discontinued because they use chlorofluorocarbons (CFCs) to move the medicine out of the inhaler so patients can breathe the medicine into their lungs. CFCs harm the environment by decreasing the earth’s ozone layer. This layer of the atmosphere protects us from some of the sun’s harmful ultraviolet radiation, which can increase the risk of skin cancers and cataracts.

And here’s more news for inquiring minds and curious health-conscious consumers.

The FDA’s MedWatch Safety Alerts for February 2011 includes two recalls:

1. Svelte 30 orange & gray capsules marketed as a natural herb for weight loss and two lots of counterfeit Extenze Tablets—both sold as dietary supplements—were found to contain sibutramine, a controlled substance that was withdrawn from the market in October 2010 for safety reasons. Do not use the Svelte 30 or Extenze products described above. Return them to the place where you bought them for a refund.
2. Triad alcohol prep pads, swabs, and swabsticks, sold over-the-counter by themselves or packaged with some medical devices and prescription medicines for injection may be contaminated. The recalled disinfecting products list the manufacturer as either “Triad Group” or one of the following names: Cardinal Health, PSS Select, VersaPro, Boca/Ultilet, Moore Medical, Walgreens, CVS, and Conzellin. Do not use any of the products listed above. Return them to the place where you bought them for a refund.

Get Resourceful

FDA Consumer Updates by email are free for the asking.

Food Recalls, Market Withdrawals, and Safety Alerts [www.fda.gov/Safety/Recalls/default.htm] are also available.

To report a serious medical product problem to FDA’s MedWatch Adverse Event Reporting Program, go online (see left side of page) or call 1-800-332-1088.

Source: FDA Consumer Health Information, www.fda.gov/ForConsumers

How to Keep Updated on Drug Safety The Saturday Evening Post