[Recalled] FLUTTER Percussor respiratory device, packaged one unit per clear plastic package. Product Usage: Product is a percussor device, intended to be used as a mucus clearance device for patients with mucus producing respiratory
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | FLUTTER Percussor respiratory device, packaged one unit per clear plastic package. Product Usage: Product is a percussor device, intended to be used as a mucus clearance device for patients with mucus producing respiratory conditions such as: atelectasis, bronchitis, bronchiectasis, cystic fib |
|---|---|
| Brand / manufacturer | Aptalis Pharmatech Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1006-2015 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 13 November 2014 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Customer notification that the device may be difficult to open or close.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.