Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cannulaide Recalled by Beevers Manufacturing & Supply, Inc. Due to Cannulaide recalled May 2008 due to improper seal...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Beevers Manufacturing & Supply, Inc. directly.
Affected Products
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.
Quantity: 16,575 units total (15,625 units in US and 950 units outside US)
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 7 states: CA, FL, GA, LA, MA, NJ, OR
About Beevers Manufacturing & Supply, Inc.
Beevers Manufacturing & Supply, Inc. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report