Drug recall
Cannulaide, Model 101, 102, 103. Respirator. The Cannulaide product is composed of die-cut hydrocolloid-coated…
FDA recall event 69627 · Class II · Beevers Manufacturing & Supply, Inc.
Key facts
| Event ID | 69627 |
|---|---|
| Recall numbers | Z-0483-2015 |
| Recalling firm | Beevers Manufacturing & Supply, Inc. |
| Product type | Devices |
| 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | May 13, 2008 |
| Report date | Dec 3, 2014 |
| Termination date | Nov 28, 2014 |
| City | McMinnville |
| State | OR |
| Country | United States |
| FEI number | 3023468 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: