Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
FLUTTER Percussor respiratory device Recalled by Aptalis Pharmatech Inc. Due to Customer notification that the device may be difficult...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Aptalis Pharmatech Inc. directly.
Affected Products
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 fibrous, chronic obstructive pulmonary disease (COPD) and asthma.
Quantity: Approximately 49,000 units
Why Was This Recalled?
Customer notification that the device may be difficult to open or close.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Aptalis Pharmatech Inc.
Aptalis Pharmatech Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report