Some salsalate recalled

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Actavis Totowa LLC, a generic drug manufacturer, has voluntarily

Recalled all drug products manufactured at its Little Falls, New

Jersey facility. An FDA inspection at Little Falls revealed

Operations which did not meet the FDA's or Actavis' standards

For good manufacturing practices.

This recall includes all AMIGESIC 500 mg and 750 mg CAPLETS

Manufactured by Actavis Totowa, LLC.

For more information, please visit: http://www .FDA.gov/O

C/Po/firmr ecalls/act avis08_08. HTML or http://www .actavis.U

S/RecallFAQ

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WHAT DOES THIS MEAN?

IGuard is currently monitoring safety alerts for SALSALATE. If

You are still using this medication, look at your bottle to see

If it was manufactured by Actavis Totowa LLC - or take your

Bottle to your pharmacy for your pharmacist to check.

This recall is not associated with a product complaint or health

Hazard. As a result, if you are using medications covered by

This recall you should continue to take them as directed until

You speak with your pharmacist - the risk of suddenly stopping

This medication is likely to be greater than any risk associated

With their manufacturing. Most pharmacies will provide you with

Replacement medication if you return with your original bottle.

For updated risk ratings on all of your registered medications,

Or to update your medication list, please log into your profile

(https://secure.iGuard.org/user). You can also reach your

Profile by clicking on the link in the top right corner of any

Page on our web site.

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