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      Medical Device Recall News Release

      Health & Life Co., LTD. Issues Nationwide Recall of EZ Breathe™ Atomizer, Model #EZ-100


      News provided by

      Nephron Pharmaceuticals Corporation

      May 08, 2013, 05:12 ET

      Share this article

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      NEW TAIPEI CITY, Taiwan, May 8, 2013 /PRNewswire/ --

      Recall Managed By: Nephron Pharmaceuticals Corporation
      Health & Life Co., LTD
      9F, No. 186, Jian Yi Road
      Zhonge District 23553         
      New Taipei City, Taiwan
      886.2.82271300   www.healthandlife.com.tw

      Continue Reading
      Nephron Pharmaceuticals Corporation
      Nephron Pharmaceuticals Corporation
      Nephron Pharmaceuticals Corporation
      Nephron Pharmaceuticals Corporation
      Nephron Pharmaceuticals Corporation
      Nephron Pharmaceuticals Corporation
      Nephron Pharmaceuticals Corporation
      Nephron Pharmaceuticals Corporation
      Nephron Pharmaceuticals Corporation
      Nephron Pharmaceuticals Corporation

      On May 8, 2013, Health & Life, Co., LTD, initiated a nationwide recall of 242,892 EZ Breathe™ Atomizers, Model #EZ-100, after becoming aware of an increase in the number of complaints.  The Atomizers have been determined to have the possibility of a manufacturing defect which results in a quarter-inch diameter washer becoming dislodged from the EZ Breathe™ Atomizer, which potentially could result in a choking hazard.  This product is manufactured by Health & Life Co., LTD. in Taiwan for Nephron Pharmaceuticals Corp.,  who is managing the recall activities.  No injuries have been reported to date.

      The EZ Breathe™Atomizer can be found in these three presentations:

      1) Packaged in the Asthmanefrin® Starter Kit, NDC 0487-2784-10.  Each Asthmanefrin® Starter Kit contains 10 vials of Asthmanefrin® medication that are manufactured by Nephron Pharmaceuticals Corp. and one EZ Breathe™ Atomizer.

      Affected Asthmanefrin® Starter Kit Lot #'s: R2029A, R2029B, R2039A, R2042A, R2045A, and R2047A.

      (Photo: http://photos.prnewswire.com/prnh/20130508/FL10469-a )

      2) EZ Breathe™ Atomizers Model # 100 
      Affected Atomizer Serial Number Ranges:

      1206034476 - 1206069065

      1209069180 - 1209069202

      1207003710 – 1207038299

      1209069203 – 1209069460

      1207046505 – 1207081124

      1210000001 - 1210103680

      1208027421 - 1208062155

      1210104001 - 1210104044

      1209000001 - 1209069179

      Serial numbers can be identified on the
      battery door of the atomizer (see below)

      (Photo: http://photos.prnewswire.com/prnh/20130508/FL10469-b )
      (Photo: http://photos.prnewswire.com/prnh/20130508/FL10469-c )
      (Photo: http://photos.prnewswire.com/prnh/20130508/FL10469-d )

      3) Replacement Medication Cup
      Affected Lot #'s: 120902, 120903 and 120904 
      (lot numbers are found on the medication cup packaging)

      (Photo: http://photos.prnewswire.com/prnh/20130508/FL10469-e )

      Recalled  EZ Breathe™ Atomizers were manufactured from May 21, 2012 through October 29, 2012 and distributed from August 3, 2012 through April 24, 2013.

      This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

      Nephron Pharmaceuticals Corp. is notifying its distributors and customers by either direct mail, email or telephone and is arranging for the return of all recalled Atomizers.  Nephron Pharmaceuticals Corp. distributed  EZ Breathe™ Atomizers contained in Asthmanefrin® Starter Kits nationwide to drug wholesalers, pharmacies and individuals.

      Consumers who have affected EZ Breathe™ Atomizers (as referenced above) should stop using, and contact the EZ Breathe Atomizer Recall Customer Care Center at 1-855-413-8920, between the hours of 8:00 am and 5:00 pm EDT, for return and replacement of their EZ Breathe™ Atomizer at no charge. 

      Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA:

      • Online at http://www.fda.gov/Safety/MedWatch/HowToReport/default.htm1 (form available to fax or mail), or call FDA 1-800-FDA-1088

      SOURCE Nephron Pharmaceuticals Corporation

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