The Recall Desk

Manufacturer

Aptalis Pharmatech Inc.

1 recall in our database name Aptalis Pharmatech Inc. as the manufacturing or recalling firm.

What the numbers show

Total
1
Critical
0
Severe
0
Most recent
2015-01-28

Of the 1 recalls from Aptalis Pharmatech Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–1 of 1

  • LowFDA (Devices)·Z-1006-2015·2015-01-28

    Aptalis Flutter Percussor Respiratory Device Recalled for Packaging Defect

    Aptalis Pharmatech Inc. is recalling approximately 49,000 Flutter Percussor respiratory devices because the packaging may be difficult to open or close.

    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, bronch
    Category
    Medical Device
    Distribution
    Distributed nationwide