Beevers Manufacturing & Supply, Inc. recalls Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethane film with an integ

Recalled December 10, 2014 · FDA recall Z-0487-2015 · Beevers Manufacturing & Supply

Hazard

Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102. · FDA Class II

Units

393 units

Sold at

Worldwide Distribution: US (nationwide) and country of: ME-Musaffah.

Description

Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.

Product

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.

Manufacturer(s)

Beevers Manufacturing & Supply, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →