FDA recall record

Compass Health Brands Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage recall — FDA Z-1720-2015

Roscoe Medical has recently identified the need to update its user manual with additional warning statements regarding proper handling and storage of the…

Class IIclassification
Z-1720-2015official record ID
Jun 17, 2015report date

Recall record at a glance

Official recordZ-1720-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCompass Health Brands
Report dateJun 17, 2015
Recall initiation dateApr 20, 2015
Quantity219,353 Manuals
LocationStrongsville, OH, United States

Official product description

Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage: Inhaler therapy that converts liquid medicine into a fine mist that is easily inhaled.

Why the product was recalled

Roscoe Medical has recently identified the need to update its user manual with additional warning statements regarding proper handling and storage of the nebulizer. These warnings are to better inform end users of proper care when using and storing a Roscoe Medical Nebulizer to reduce user damage (wear & tear) to the power cord.

Distribution information

Worldwide Distribution US nationwide in the states of: AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV & WY and countries of:: Australia, Canada, Chile, Colombia, Costa Rica, Dominican Republic, Ecuador, France, Hong Kong, India, Norway, Spain, Trinidad and Tobago & United Kingdom.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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