Smiths Medical ASD Inc. recalls Portex Acapella DH Vibratory PEP Device - Product Usage: a s
Recalled Product
Portex Acapella DH Vibratory PEP Device - Product Usage: a single patient use device that provides Positive Expiratory Pressure (PEP) Therapy for patients who have Cystic Fibrosis, COPD, asthma, and lung diseases with secretory problems, and patients with atelectasis.
Hazard / Issue
Shipping box may contain wrong model.
Issued by
FDA
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