Aptalis Pharmatech FLUTTER Percussor respiratory device, packaged one unit per clear plastic recall — FDA Z-1006-2015
Customer notification that the device may be difficult to open or close.
Overview of recall records associated with Aptalis Pharmatech Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Customer notification that the device may be difficult to open or close.
This page summarizes recall records in which the official source identifies Aptalis Pharmatech Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.