Drug recall
Airways Development LLC WaterPAP Positive Airway Pressure Device Reference #WP-7700.
FDA recall event 72848 · Class II · Airways Development LLC
Key facts
| Event ID | 72848 |
|---|---|
| Recall numbers | Z-0552-2016 |
| Recalling firm | Airways Development LLC |
| Product type | Devices |
| Products | Airways Development LLC WaterPAP Positive Airway Pressure Device Reference #WP-7700. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Airways Development LLC has received a complaint about a canister leaking from WaterPAP Lot 8605A. During a review with their supplier it could not be determined if this was an isolated incident or if… |
| Initiation date | Sep 24, 2015 |
| Report date | Dec 30, 2015 |
| Termination date | May 9, 2016 |
| City | Kenilworth |
| State | NJ |
| Country | United States |
| FEI number | 3000210458 |
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: