... other interested parties. Although FDA approves medical products, FDA does not endorse either the product or the company. This is the retyped text of a letter from Schering / Key. Contact the company for a copy of any referenced enclosures. URGENT-DRUG PRODUCT RECALL Schering / Key PROVENTILÂ ® brand of albuterol, USP Inhalation Aerosol (17g / 200 inhalations). PROVENTILÂ ® brand of albuterol, USP Inhalation Aerosol Refill (17g / 200 inhalations). PROVENTILÂ ® brand of albuterol, USP, Inhalation Aerosol Institutional Pack (6.8 ... for Human Medical Products 2005 Safety Alerts for Human Medical Products 2004 Safety Alerts for Human Medical Products 2003 Safety Alerts for Human Medical Products 2002 Safety Alerts for Human Medical Products 2001 Safety Alerts for Human Medical Products 2000 Safety Alerts for Human Medical Products-Proventil (albuterol) Dear Healthcare Professional Letter Mar 2000 FDA posts safety alerts, public health advisories, press releases and other notices from companies as a service to health professionals, consumers and other interested parties. Although FDA approves medical products, FDA does not endorse either the product or ...

... copy of any referenced enclosures. FOR IMMEDIATE RELEASE Contact: Robert J. Consalvo (973) 822-7409 SCHERING LABORATORIES RECALLS CERTAIN AEROSOL INHALERS MANUFACTURED PRIOR TO SEPT. 30, 1999 KENILWORTH, N.J, March 29, 2000 â €“ Schering Laboratories is voluntarily conducting a recall of certain prescription inhalation aerosol asthma products (see table below) that were manufactured prior to Sept. 30, 1999, with the exception of those already-opened PROVENTILà ’ albuterol inhalers and PROVENTIL inhaler refills or Warrick brand of albuterol inhalers and Warrick inhaler refills that are currently ... used by asthma patients with good results. Schering Laboratories is issuing this recall as a precaution to address the remote possibility that an aerosol inhaler may not contain active drug, although the company believes that all of its aerosol products currently in the marketplace are safe and effective. Asthma patients who are using their already-opened PROVENTIL or Warrick brand of albuterol inhalers with good results do not need to replace those individual units, regardless of when the inhalers were manufactured. Product Lot Numbers*Patient Action PROVENTIL and Warrick brand of (albuterol, USP ...

... for Human Medical Products 2005 Safety Alerts for Human Medical Products 2004 Safety Alerts for Human Medical Products 2003 Safety Alerts for Human Medical Products 2002 Safety Alerts for Human Medical Products 2001 Safety Alerts for Human Medical Products 2000 Safety Alerts for Human Medical Products-Aerosol Inhalers Recall -Proventil (albuterol) & Vanceril (beclomethasone dipropionate) Schering Laboratories is voluntarily recalling certain prescription inhalation aerosol asthma products that were manufactured prior to Sept. 30, 1999, with the exception of those already-opened Proventil albuterol inhalers and Proventil inhaler refills or Warrick brand of albuterol ... and Warrick inhaler refills that are currently being used by asthma patients with good results. [March 29, 2000-Letter -Proventil-Schering Laboratories] [March 29, 2000-Letter -Vanceril 42 mcg & 84 mcg-Schering Laboratories] [March 29, 2000-Press Release-Schering Laboratories]-- Links on this page: Page Last Updated: 07 / 31 / 2009 Note: If you need help accessing information in different file formats, see Instructions for Downloading Viewers and Players. Home About FDA Contact Us A ...

... Drugs and Therapeutic Biological Products Product Name Date Issued / Updated Albuterol Sulfate Inhalation Solution unit-dose vials (Dey LP brand) 09 / 10 / 2009 Alka-Seltzer Plus Day & Night Cold Formula Liquid Gels-Incorrect Packaging 12 / 09 / 2009 Atlas Operations, Inc: Recall of Sexual Enhancement Products 04 / 14 / 2010 Dietary Supplements Sold on Internet by Bodybuilding.com 11 / 03 / 2009 Body Building Products (Marketed as Containing Steroids or Steroid-like Substances) 07 / 28 / 2009 Botox and Botox Cosmetic (Botulinum toxin Type A) and Myobloc ... Issued" to re-order the items in a list by date. Click" Product Name" to re-order the items alphabetically. MedWatch" What's New" Archive, May 29-Dec 31, 2009-Drugs and Therapeutic Biological Products Product Name Date Issued / Updated Albuterol Sulfate Inhalation Solution unit-dose vials (Dey LP brand) 09 / 10 / 2009 Alka-Seltzer Plus Day & Night Cold Formula Liquid Gels-Incorrect Packaging 12 / 09 / 2009 Atlas Operations, Inc: Recall of Sexual Enhancement Products 04 / 14 / 2010 Dietary Supplements Sold ...

... in alphabetical order. Click" Date Issued" to re-order the items in a list by date. Click" Product Name" to re-order the items alphabetically.-Drugs Product Name Date Issued / Updated Accolate (zafirlukast) 09 / 15 / 2000 Aerosol Inhalers Recall -Proventil (albuterol) & Vanceril (beclomethasone dipropionate) 03 / 29 / 2000 Agenerase (amprenavir) 05 / 01 / 2000 Clinipad Corporation Products 03 / 09 / 2000 Colchicine 12 / 23 / 2000 Depakote (divalproex sodium delayed-release tablets) and Depakote (divalproex sodium ... particles in capsules) 07 / 31 / 2000 Depacon (valproate sodium injection) 07 / 31 / 2000 Depakene (valproic acid capsules and syrup) 07 / 31 / 2000 Eskalith CR (lithium carbonate) 03 / 17 / 2000 Etodolac Capsules 300 mg 10 / 06 / 2000 Sterile FUDR (floxuridine) 01 / 24 / 2000 Fluothane (halothane, U.S.P) 03 / 10 / 2000 Lamictal (lamotrigine) Tablets and Lamisil (terbinafine hydrochloride) Tablets 06 / 28 / 2000 Lithobid (lithium carbonate 300 mg slow-release tablets) ...