FDAFDA · Food and drugs·Recall number Z-0487-2015
Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethane film with an integral hook strip (i.e., Velcro) to allow for the use of a loop material to help secure a nasal interface. The Cannulaide is applied under and over the nose of infants to provide a protective barrier to the philtrum, columella, septum, nares, and tip of nose. It is available in multiple sizes that vary the external geometry and nare hole size and spacing to allow for use on infants ranging from less than 700 grams to greater than 3000 grams. It is a non sterile, single patient use, disposable device.
Published December 10, 2014 · Recall initiated: January 18, 2007
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Beevers Manufacturing & Supply, Inc.
- Distributor
- Worldwide Distribution: US (nationwide) and country of: ME-Musaffah.
- Lot
- Lot 20060928. Product expired in 2009.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.