Moog Medical Devices Group Expands Administration Set Recall

Moog Medical Devices Group Expands Administration Set Recall 
SALT LAKE CITY, UT -- (Marketwire) -- 01/21/13 --  Moog Medical
Devices Group (MMDG) is expanding a previous recall (Z-1659-2012
through Z-1672-2012) communicated in May 2012 and related to a
reverse pump segment in one of its administration sets. The recall
expansion affects the United States only and a single additional
product lot containing 1,820 administration sets total. The affected
product information is listed below: 
Administration Set Part Number: 340-4114, Lot Number: CF1210880 
As of the date of this release, MMDG has not received any reports
injury or death as a result of this recall. 
Direct customers and distributors will be notified of the process for
obtaining replacement administration sets. Patients in a home
environment, please contact your home healthcare provider or
clinician for proper handling and the replacement process of your
affected set(s). Contact the Moog Medical Customer Advocacy Group at
(800) 970-2337 if you have questions about this recall expansion. 
For more information on the original administration set recall please
Adverse reactions or quality problems experienced with the use of
this product may be reported to the FDA's MedWatch Adverse Event
Reporting program either online, by regular mail or by fax. 
Regular Mail:        
 Use postage-paid FDA form 3500 available at: 
 Mail to MedWatch 5600
Fishers Lane, 
 Rockville, MD 20852-9787    
About Moog
 Moog Inc. is a worldwide designer, manufacturer, and
integrator of precision control components and systems. Moog's
high-performance systems control military and commercial aircraft,
satellites and space vehicles, launch vehicles, missiles, automated
industrial machinery, wind energy, marine and medical equipment.
Additional information about the company can be found at 
Shaunalee Wall 
Product Information
801-264-1001 x297 
Ann Marie Luhr
Investor Relations
FAX -716/687-4457 
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