FDA Device recall Z-0487-2015
Cannulaide, Model 101
- FDA Device
- Class II
- terminated
- Published 2014-12-10
On 2014-12-10 the FDA classified a Class II recall of Cannulaide, Model 101 by Beevers Manufacturing And Supply, citing cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0487-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2007-01-18 |
| Published | 2014-12-10 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Beevers Manufacturing And Supply |
| Distribution | US |
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
Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.
Identifiers
| code_info | Lot 20060928. Product expired in 2009. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0487-2015%22
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