Cannulaide, Model 101, 102, 103. Respirator. The Cannulaide product is composed of die-cut h...
FDA Recall #Z-0483-2015 — Class II — May 13, 2008
Product Description
Cannulaide, Model 101, 102, 103. Respirator. 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.
Reason for Recall
Cannulaide recalled May 2008 due to improper seal of the pouch. The improper seal of the Cannulaide's package could potentially affect the device shelf life.
Recalling Firm
Beevers Manufacturing & Supply, Inc. — McMinnville, OR
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
16,575 units total (15,625 units in US and 950 units outside US)
Distribution
Worldwide Distribution - US Distribution including the states of LA, GA, OR, MA, NJ, FL and CA., and the countries of Canada, France, Japan, Netherlands and United Kingdom.
Code Information
CA 101: Lot 54219; CA 102: Lot 52834; CA 103: Lot 53813;
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated