Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage:… — Class II medical device recall Z-1720-2015
Terminated recall by Compass Health Brands, reported 2015-06-17, distributed nationwide. Roscoe Medical has recently identified the need to update its user manual with additional warning statements r
| Recall number | Z-1720-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Compass Health Brands, Strongsville, OH, United States |
| Recall initiated | 2015-04-20 |
| Classified | 2015-06-05 |
| Reported by FDA | 2015-06-17 |
| Terminated | 2016-10-25 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CL, CO, CR, DO, EC, ES, FR, GB, HK, IN, NO, TT |
| Quantity | 219,353 manuals |
Product
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.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1720-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.