FDA Device recall Z-0552-2016
Airways Development LLC WaterPAP Positive Airway Pressure Device Reference #WP-7700
- FDA Device
- Class II
- terminated
- Published 2015-12-30
On 2015-12-30 the FDA classified a Class II recall of Airways Development LLC WaterPAP Positive Airway Pressure Device Reference #WP-7700 by Airways Development, citing 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 is….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0552-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-09-24 |
| Published | 2015-12-30 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Airways Development |
| Distribution | US |
Product
Airways Development LLC WaterPAP Positive Airway Pressure Device Reference #WP-7700.
Reason
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 the whole lot is impacted.
Identifiers
| code_info | Reference #WP-7700; Lot 8605A |
|---|
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-0552-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.