Beevers Manufacturing & Supply, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0487-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: January 18, 2007

Date Posted: December 10, 2014

Recall Number: Z-0487-2015

Event ID: 69648

Reason for Recall:

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

Status: Terminated

Product Quantity: 393 units

Code Information:

Lot 20060928. Product expired in 2009.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated