Cannulaide — Class II medical device recall Z-0487-2015

Terminated recall by Beevers Manufacturing & Supply, Inc., reported 2014-12-10, distributed nationwide. Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.

Recall number	`Z-0487-2015`
Product type	Medical device
Classification	Class II
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	Beevers Manufacturing & Supply, Inc., McMinnville, OR, United States
Recall initiated	2007-01-18
Classified	2014-12-01
Reported by FDA	2014-12-10
Terminated	2014-12-01
Distributed	Nationwide (US)
Quantity	393 units
Reason classes	labeling
Lot numbers	`20060928`
Model numbers	`101`

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.

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0487-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.