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Recall of Infant and Neonatal-Sized FilterLine H Set and VitaLine H Set Sampling Lines
Date:5/20/2011

">http://www.philips.us/filter.  New products are being supplied to affected customers at no charge.

Philips has notified the FDA of its decision to voluntarily recall the affected product.  Customers who have questions about the recall or wish to report product problems may contact their local Philips Representative.

Any adverse events experienced with the use of this product should be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088, by fax at 1-800-FDA-0178, by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at www.fda.gov/medwatch.


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