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  2. Skechers Shape-Ups ad claims said to be misleading ... - AOL

    www.aol.com/news/2010-09-01-skechers-shape-ups...

    Skechers, the go-to brand for cheerleader sneakers, is facing a federal class-action lawsuit over allegedly exaggerating the health benefits of its hot-selling Shape-Ups line and reaping "millions ...

  3. FTC to Skechers: You'd Better Shape Up - AOL

    www.aol.com/news/2012-05-19-ftc-to-skechers-youd...

    It was a sketchy claim to begin with: Just wearing Skechers (NYS: SKX) toning sneakers would let you lose weight; firm up your legs, behind, and abdomen; and close the national debt faster than ...

  4. Skechers - Wikipedia

    en.wikipedia.org/wiki/Skechers

    Skechers was founded in 1992 by Robert Greenberg, who had previously founded LA Gear in 1983 (he stepped down as CEO of that company the same year he founded Skechers). Greenberg sought to focus on men's street shoes; Skechers' early products were utility-style boots popular in grunge fashion. [3]

  5. Skechers draw backlash for full-page ad in Vogue that reeks ...

    www.aol.com/finance/skechers-draw-backlash-full...

    The realization made the @polishlaurapalmer turn on the ad and Skechers itself. Calling the image “alarmingly ugly,” she issued a warning for companies looking to hastily integrate AI. Screen ...

  6. Rocker bottom shoe - Wikipedia

    en.wikipedia.org/wiki/Rocker_bottom_shoe

    The shoes are generically known by a variety of names, including round bottom shoes, [1] round/ed sole shoes, [2] and toning shoes, [3] but also by various brand names. [4] Tyrell & Carter identified at least six standard variations of the rocker sole shoe and named them: toe-only rocker , rocker bar , mild rocker , heel-to-toe rocker ...

  7. FDA recall policies - Wikipedia

    en.wikipedia.org/wiki/FDA_recall_policies

    FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.

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