Beevers Manufacturing & Supply, Inc. 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 inf Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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 inf
Brand
Beevers Manufacturing & Supply, Inc.
Lot Codes / Batch Numbers
Lot 20060928. Product expired in 2009.
Products Sold
Lot 20060928. Product expired in 2009.
Beevers Manufacturing & Supply, Inc. is recalling Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethan due to Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.
Recommended Action
Per FDA guidance
Beevers Manufacturing and Supply, Inc. (BMS) of McMinnville, Oregon, began notifying consignees about this recall on 1/18/2007. Customers were advised to inspect blue box that say size 2 (CA 102) and check if size 1 (CA 101) was packed inside. Salter Labs provided BMS' recall report to FDA in October 2014.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026