Cannulaide — Class II medical device recall Z-0483-2015
Terminated recall by Beevers Manufacturing & Supply, Inc., reported 2014-12-03, distributed in CA, FL, GA, LA, MA, NJ, OR. Cannulaide recalled May 2008 due to improper seal of the pouch. The improper seal of the Cannulaide's package
| Recall number | Z-0483-2015 |
|---|---|
| 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 | 2008-05-13 |
| Classified | 2014-11-26 |
| Reported by FDA | 2014-12-03 |
| Terminated | 2014-11-28 |
| Distributed | CA, FL, GA, LA, MA, NJ, OR |
| Countries outside the US | CA, FR, GB, JP, NL |
| Reason classes | packaging |
| Lot numbers | 102, 103, 52834, 53813, 54219 |
| Model numbers | 101, 102, 103 |
Product
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.
Reason for recall
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.
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-0483-2015. 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.